PARTICLE-MEDIATED DELIVERY OF BIOLOGICS
A composition for delivering a biologic to a subject generally includes a particulate substrate and an mRNA encapsulated by the particulate substrate. In some cases, the mRNA bay be indirectly attached to the particulate substrate. The mRNA encodes at least one therapeutic polypeptide. The composition may be delivered to a tissue of a subject to provide a therapeutic benefit to the tissue.
This application claims priority to U.S. Provisional Patent Application No. 62/426,090, filed Nov. 23, 2016, which is incorporated herein by reference in its entirety.
BACKGROUNDA heart attack, also called a myocardial infarction, occurs when a part of the heart muscle does not receive enough blood flow. The more time that passes without treatment to restore blood flow, the greater the damage to the heart muscle. Every year, about 735,000 Americans have a heart attack, including about 210,000 heart attacks that happen to people who have already had a first heart attack (Mozaffarian et al., Circulation, 131(4):e29-322 (2015)).
SUMMARYThis disclosure describes modifications to RNA molecules that increase the length of time that the modified RNA molecules exist in cells.
This disclosure further provides materials and methods for particle-mediated delivery of one or more biologics (e.g., RNA, modified RNA, and/or microvesicles) to a tissue (e.g., heart tissue). Microvesicles can represent manufactured particles or naturally occurring structures, such as exosomes. For example, this document provides particles (e.g., alginate gels) for delivering one or more RNAs to cardiac tissue to improve cardiac function.
As demonstrated herein, an alginate gel can be used to deliver mRNA to a heart tissue where the mRNA can be translated into a functional polypeptide. Particle-mediated delivery of RNA can induce robust and sustainable RNA expression. In some cases, particles can be used be designed to control temporal and/or spatial delivery of one or more encapsulated molecules (e.g., biologics).
In one aspect, therefore, this disclosure describes composition that generally include a particulate substrate and an mRNA attached to the particulate substrate. The mRNA includes at least one modification to inhibit degradation of the mRNA when the mRNA is in cytosol of a cell. The mRNA also encodes at least one therapeutic polypeptide. In some embodiments, the mRNA modification comprises a pseudoknot, an RNA stability element, or an artificial 3′ stem loop. In some embodiments, the particulate substrate can include a chemical modification of its surface. In various embodiments, the particulate substrate can include a nanoparticle, a plurality of nanoparticles, or a microparticle. In some embodiments, the therapeutic polypeptide can include an immunoglobulin heavy chain or an immunoglobulin light chain.
In general, one aspect of this document features a method for improving cardiac function. The method includes, or consists essentially of, administering a particle encapsulating an mRNA encoding a polypeptide useful for regenerating cardiac function and/or tissue to a mammal, thereby improving cardiac function of the mammal. The polypeptide can be NAP-2, TGF-a, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, and/or CD80/86. The mammal can be a human. The human can have undergone percutaneous coronary intervention for ST-elevation myocardial infarction. The administering can be an arterial administration. The particle can include alginate. The alginate can be in the form of an alginate gel. The alginate gel can include a calcium salt. The alginate gel including a calcium salt can have a ratio of alginate to calcium salt that can be from about 2:1 to about 10:1. The particle can be from about 5 μm to about 10 μm in diameter. The particle can be a biphasic particle. The biphasic particle can be a polarized particle. The biphasic particle can have a tail. The method can include administering the composition during a percutaneous coronary intervention. The particle can include a scaffold protein (e.g., collagen I, collagen II, collagen III, collagen IV, fibrin, and/or gelatin). The particle can encapsulate a polypeptide (e.g., an antibody having the ability to neutralize tumor necrosis factor activity, an antibody having the ability to neutralize mitochondrial complex-1 activity, or a resolvin-D1 agonist). The particle can encapsulate a lipopolysaccharide. The particle can encapsulate a microvesicle and/or exosome.
In another aspect, this document features a method for improving cardiac function in a mammal. The method includes, or consists essentially of, administering to a mammal a particle encapsulating an inhibitory RNA having the ability to reduce expression of a polypeptide selected from the group consisting of eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-a, IL-21, NOV, transferrin, TIMP-2, TNFaRI, TNFaRII, angiostatin, CCL25, ANGPTL4, and MMP-3, thereby improving cardiac function of the mammal. The mammal can be a human. The human can have undergone percutaneous coronary intervention for ST-elevation myocardial infarction. The administering can be an arterial administration. The particle can include alginate. The alginate can be in the form of an alginate gel. The alginate gel can include a calcium salt. The alginate gel including a calcium salt can have a ratio of alginate to calcium salt that can be from about 2:1 to about 10:1. The particle can be from about 5 μm to about 10 μm in diameter. The particle can be a biphasic particle. The biphasic particle can be a polarized particle. The biphasic particle can include a tail. The method can include administering the composition during a percutaneous coronary intervention. The particle can include a scaffold protein (e.g., collagen I, collagen II, collagen III, collagen IV, fibrin, and/or gelatin). The particle can encapsulate a polypeptide (e.g., an antibody having the ability to neutralize tumor necrosis factor activity, an antibody having the ability to neutralize mitochondrial complex-1 activity, or a resolvin-D1 agonist). The particle can encapsulate a lipopolysaccharide. The particle can encapsulate a microvesicle and/or exosome.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Methods and materials are described herein for use in the present disclosure; other, suitable methods and materials known in the art can also be used. The materials, methods, and examples are illustrative only and not intended to be limiting. All publications, patent applications, patents, sequences, database entries, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
The RNA stability element acts as a decoy to block UPF1 contact with the 3′UTR avoiding activation of the NMD. Poly(A) tail stem loop structures are used to diminish exosome-mediated mRNA degradation in constructs where a CAP/PABP independent IRES platform is used.
This disclosure relates to materials and methods for particle-mediated delivery of biologics (e.g., RNA and/or microvesicles) to tissue (e.g., heart tissue). This disclosure further describes modifications to RNA that increase the length of time that the modified mRNA molecules exist in cells and, therefore, the length of time that the modified mRNA molecules can be translated into produce polypeptides encoded by the modified mRNA.
This disclosure provides materials and methods for particle-mediated delivery of one or more biologics (e.g., RNA and/or microvesicles) to a mammal. For example, a particle (e.g., an alginate gel) described herein can be used to encapsulate RNA and deliver the encapsulated RNA to a tissue in a temporally and/or spatially specific manner. As used herein, the term “encapsulate” and variations thereof is used broadly to refer to any method by which a biologic is housed within a particle or bound, directly or indirectly, to the outer surface of a particle. As explained in more detail below, the particle can be nanoparticulate or microparticulate in scale. Thus, the term “encapsulate” includes, but does not require, that the particle completely surround the material being encapsulated. Rather, a material is encapsulated if it is merely captured to any degree within the dimensions of the particle, including any surface modifications. Surface modifications of the particle can facilitate indirect binding of the encapsulated material to the particle. In addition, macroencapsulation can be used to deliver a biologic by providing a protective vehicle by which to transmit the biologics either by direct injection or through a blood vessel into a target tissue.
In some cases, one or more particles (e.g., alginate gels) containing one or more biologics (e.g., RNAs and/or microvesicles) can be used to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent percutaneous intra intervention (PCI) for ST-elevation myocardial infarction (STEMI)).
In some cases, one or more particles (e.g., an alginate gels) containing one or more biologics (e.g., RNAs or microvesicles) can be used to improve cardiac function.
In some cases, a particle (e.g., an alginate gel) described herein can store mRNA within its interior, and release (e.g., deliver) the mRNA to a tissue (e.g., heart tissue) where the mRNA is expressed as a functional protein. For example, one or more particles containing one or more mRNAs can be used to increase expression of polypeptides useful for regenerating cardiac function and/or tissue (e.g., POU homeodomain proteins (such as Oct-4), NK2 homeobox proteins (e.g., NKX2 proteins), myocyte enhancing factors (e.g., MEF2), GATA binding proteins (e.g., GATA1, GATA2, GATA3, GATA4, GATA5, and GATA6), T-box transcription factors (e.g., TBX1, TBX2, TBX3, TBX4, TBX5, TBX6, TBX10, TBX15, TBX18, TBX19, TBX20, TBX21, and TBX22), mesoderm posterior proteins (e.g., MESP1 and MESP2), neutrophil-activating proteins (e.g., NAP-2 and NAP-3), transforming growth factors (e.g., TGF-α and TGF-β), erythroblastic leukemia viral oncogene-3 (ErBb3), vascular endothelial growth factor (VEGF), insulin-like growth factor 1 (IGF-1), fibroblast growth factor (FGF-2), platelet-derived growth factors (e.g., PDGFA, PDGFB, PDGFC, and PDGFD), Interleukin-2 (IL-2), CD19, CD20, and CD80/86).
In some cases, a particle (e.g., an alginate gel) described herein can store inhibitory RNA within its interior, and release (e.g., deliver) the inhibitory RNA to a tissue (e.g., heart tissue) where the inhibitory RNA inhibits or reduces expression of a protein. For example, one or more particles containing one or more inhibitory RNAs can be used to decrease expression of one or more of the following polypeptides: eotaxin-3, cathepsin-S, Dickopf-1 (DK-1), follistatin, suppression of tumorigenicity-2 (ST-2), GRO-α, interleukin-21 (IL-21), nephroblastoma overexpressed (NOV), transferrin, tissue inhibitor of metallopeptidase-2 (TIMP-2), tumor necrosis factor receptor-1 and -2 (TNFαRI and II), angiostatin, chemokine ligand-25 (CCL25), angiopoietin like-4 (ANGPTL4), and matrix metalloproteinase-3 (MMP-3).
ParticlesA particle described herein can be used for particle-mediated delivery of one or more molecules (e.g., biologics including RNA or microvesicles) to a mammal. In some cases, a particle that can be used to encapsulate one or more biologics is non-toxic, biocompatible, non-immunogenic, and/or biodegradable.
A particle that can be used to encapsulate one or more biologics as described herein can include one or more polysaccharides. Examples of polysaccharides that can be used in a particle that can be used to encapsulate one or more molecules (e.g., biologics) as described herein include, for example, guluronate, mannuronate, guluronate-mannuronate blocks, and combinations thereof such as alginate. In some cases, a particle that can be used to encapsulate one or more biologics as described herein can include alginate. An alginate in a particle that can be used to encapsulate one or more biologics as described herein can be from any appropriate source (e.g., seaweeds such as those in the genera Phaeophyceae, Rhodophyceae, Chlorophyceae, Macrocystis, and Laminaria, or bacteria such as those in the genera Pseudomonas and Azotobacter). An alginate in a particle that can be used to encapsulate one or more biologics as described herein can be an alginate salt (e.g., sodium alginate, potassium alginate, and/or calcium alginate) or alginic acid. For example, an alginate in a particle that can be used to encapsulate one or more biologics as described herein can be sodium alginate. An alginate in a particle that can be used to encapsulate one or more biologics as described herein can be in the form of a gel, a liquid, and/or a particle (e.g., a nanoparticle, a microparticle, or a macroparticle). For example, an alginate in a particle that can be used to encapsulate one or more biologics as described herein can be an alginate gel. In some cases, a particle described herein can be a liquid at the time of administration and can form a gel (e.g., can polymerize) at the administration site and/or the target site. An alginate gel can include a calcium solution (e.g., a calcium salt solution or another appropriate positively charged ionic solution). Examples of calcium salts that can be used in a calcium solution to form an alginate gel that can be used to encapsulate one or more biologics as described herein include, without limitation, calcium chloride, magnesium chloride, potassium chloride, and iron-based solutions. The ratio of alginate to calcium salt can be used to control the viscosity of the alginate gel that can be used to encapsulate one or more biologics as described herein. In some cases, the amount of alginate can be from about 0.05 percent to about 1.0 percent of the amount of calcium salt. In some cases, the ratio of alginate to calcium salt can be can be from about 2:1 to about 10:1 (e.g., from about 2:1 to about 9:1, from about 2:1 to about 8:1, from about 2:1 to about 7:1, from about 2:1 to about 6:1, from about 2:1 to about 5:1, from about 3:1 to about 10:1, from about 4:1 to about 10:1, from about 5:1 to about 10:1, from about 6:1 to about 10:1, from about 7:1 to about 10:1, or from about 8:1 to about 10:1). Examples of appropriate alginate/calcium ratios include, without limitation, those set forth in Table 1. An alginate gel encapsulating a biologic (e.g., mRNA) described herein can be made by any appropriate method. For example, an alginate gel can be made by hydrolyzing an alginate salt (e.g., sodium alginate) using a soluble calcium salt solution (e.g., calcium chloride) as a crosslinking agent.
A particle that can be used to encapsulate one or more biologics as described herein can be in the form of a liposome, an aggregate (e.g., a nano-aggregate), a capsule (e.g., a nanocapsule), a sphere (e.g., a nanosphere), a polymersome, or a micelle. A particle that can be used to encapsulate one or more biologics as described herein that is an alginate gel can be in the form of polymerized sphere. In some cases, a particle that can be used to encapsulate one or more biologics as described herein can be a liposome. Examples of liposomes include, without limitation, a multilamellar vesicle (MLV), a small unilamellar liposome vesicle (SUV), a large unilamellar vesicle (LUV), a giant unilamellar vesicle (GUV), a multivesicular vesicles (MVV), or a cochleate vesicle. A liposome can be composed of phospholipids, cholesterols, lipoproteins, fats, fatty acids, waxes, sterols, monoglycerides, diglycerides, and/or triglycerides. In some cases, a liposome is composed of phospholipids such as phosphatidic acid (phosphatidate; PA), phosphatidylethanolamine (cephalin; PE), phosphatidylcholine (lecithin; PC), phosphatidylserine (PS), phosphoinositides (e.g., phosphatidylinositol (PI), phosphatidylinositol phosphate (PIP), phosphatidylinositol bisphosphate (PIP2), and phosphatidylinositol triphosphate (PIPS)), ceramide phosphorylcholine (sphingomyelin; SPH), ceramide phosphorylethanolamine (sphingomyelin; Cer-PE), ceramide phosphoryllipid, or any combination thereof. Examples of appropriate liposomes include, without limitation, those set forth in Table 2. A liposome encapsulating a biologic (e.g., mRNA) described herein can be made by any appropriate method. For example, a liposome can be made by sonicating a dispersion of amphipatic lipids, such as phospholipids, in water.
A particle that can be used to encapsulate one or more biologics as described herein can be any size suitable for the selected delivery method. A particle that can be used to encapsulate one or more biologics as described herein can be from about 0.3 μm to about 12 μm (e.g., from about 0.5 μm to about 11.5 μm, from about 1 μm to about 11 μm, from about 2 μm to about 10.5 μm, or from about 4 μm to about 10 μm) in diameter (or as measure across the longest dimension). For example, a particle that can be used to encapsulate one or more biologics as described herein can be from about 4.5 μm to about 7.5 μm in diameter (or as measure across the longest dimension).
A particle (e.g., an alginate gel) encapsulating one or more biologics described herein also can include one or more additional molecules in order to achieve a desired property. In some cases, a particle encapsulating one or more biologics described herein can include one or more scaffold proteins. Examples of scaffold proteins include, for example, matrix proteins (e.g., collagen (e.g., collagen I/II/III/IV)), basement membrane proteins, structural proteins, gelatin, and/or fibrin) can be incorporated into a particle to provide the particle with sustained release properties. For example, an alginate gel encapsulating one or more biologics described herein can include alginate and gelatin, alginate and collagen, alginate and fibrin, or any other appropriate combination of alginate with one or more natural basement membrane proteins. In some cases, stimuli-sensitive molecules can be incorporated into a particle to provide the particle with drug release properties under specific stimuli (e.g., pH-sensitive particles and osmolarity/osmolality sensitive particles). For example, dioleoylphosphatidylethanolamine (DOPE) can be incorporated into a particle to provide a pH-sensitive particle that maintains stability at physiological pH (about pH 7.4), but destabilize under acidic conditions (e.g., about pH 3.5 to about pH 9) leading to the release of the encapsulated RNA in acidic environments.
A particle (e.g., an alginate gel) encapsulating one or more biologics described herein can be an amorphous particle having two or more distinct physical states. For example, an amorphous particle can be administered as a liquid and form a gel upon arriving at a target tissue.
A particle (e.g., an alginate gel) encapsulating one or more biologics described herein can be a biphasic particle (sometimes referred to as a Janus particle) having two or more distinct physical properties (e.g., surface chemistry) occurring on different portions of the particle surface. For example, a biphasic particle can have two or more portions that differ in hydrophilic/hydrophobic properties, polarization, solubility properties, volume percent or density of the particle composition, the presence/absence of an additional molecule (e.g., a compound providing sustained release properties), and/or the presence/absence of a tail. In some cases, a biphasic particle can be a spherical particle having hydrophilic portions and hydrophobic portions. For example, a biphasic particle can be designed to have a hydrophilic core and a hydrophilic coating. For example, a biphasic particle can be designed to have a hydrophilic core and a hydrophilic coating. In some cases, a biphasic particle can be a spherical particle having differential density. For example, a biphasic particle can be designed to have increased volume percent of an encapsulated biologic at one end of the particle. In some cases, a biphasic particle can be a spherical particle having a coating. For example, a biphasic particle can be designed to have a porous coating. In some cases, a biphasic particle can be a spherical particle having differential solubility. For example, a biphasic particle can be designed to have a first side that readily dissolves in certain physiological conditions and a second side that dissolves slowly in the same physiological conditions. In some cases, a biphasic particle can be a spherical particle having a tail extending from one portion of the particle surface. For example, a biphasic particle can be designed to guide particles in the blood flow. In some cases, a biphasic particle can be designed to have a first (e.g., leading) side that readily dissolves in certain physiological conditions and a second side that dissolves slowly in the same physiological conditions and includes a tail to guide particles in the blood flow.
A biphasic particle encapsulating one or more biologics described herein can be made using any appropriate method. In some cases, a biphasic particle can be made using stabilizer technology (e.g., including dry water approaches). For example, two or more separate soft liquid cores (e.g., two liquids having different hydrophobicity such as a hydrophobic entity and hydrophilic entity, or two liquids having different solubility such as water and an oil) can be stabilized and then merged into a biphasic particle. In some cases, a biphasic particle can be made using melt combination and fusion technology. For example, two or more separate streams (e.g., two streams of molten wax having differential properties, or two streams of polymers having different properties) can be merged (e.g., injected into a single stream) to form a biphasic particle. In some cases, a biphasic particle can be made using 3D-printer technology. For example, two or more coatings (e.g., two wax coatings having different properties) can be printed onto a particulate internal structural element (e.g., a particle of polystyrene foam such as STYROFOAM′) to form a biphasic particle. The particulate internal structural element can be removed (e.g., by acetone elimination) and replaced with one or more biologics. In some cases, a biphasic particle can be made using microfluidics technology. For example, two or more liquid flows (e.g., two liquids having different properties) can be flowed into a microfluidic channel to form biphasic droplets, which can be solidified (e.g., by thermal polymerization, elimination of sheer stress on spatially divalent particles, evaporation, coagulation, cation exposure, or pH) into biphasic particles. In some cases, a biphasic particle can be made using protection and de-protection technology. For example, a protection particle having a desired surface chemistry can be adsorbed onto a main particle; de-protection can yield the original surface of the main particle, which can be chemically modified.
In some cases, a biphasic particle can be made use other appropriate technologies. For example, other appropriate methods can include, without limitation, interfacial emulsification, acorn and dumbbell shaped formation, use of magnetic fields to shape and manipulate particles during fabrication, and direct surface coating deposition. In some embodiments, differential density can be achieved using organogels with varied density. In some embodiments, differential porosity can be achieved using salts at a particular surface of the particle. In some embodiments, differential solubility can be achieved using salts and/or using two or more different polymers (e.g., PEGs) having different solubilities. In some embodiments, various tails can be achieved using waxy components, chemically modifying (e.g., with long-chain reactants), and/or magnetizing a particle. Exemplary methods for making a biphasic particle encapsulating one or more biologics described herein are shown in
A particle (e.g. an alginate gel) encapsulating one or more biologics described herein can be used to deliver the encapsulated biologics to a target tissue (e.g., heart tissue). Mechanisms of targeting a particle described herein can include using an adhesive particle, a targeting moiety, particle size, capillary leakage in the setting of injury, capillary leakage in the setting of oncogenic neovasculogenesis, and/or direct injection (e.g., via an edema forming needle (e.g., a nitinol (nickel-titanium) helical needle) designed with graded side holes and no end hole (see, e.g.,
In some cases, an adhesive moiety can be conjugated to a particle described herein to retain an adhesive particle at the administration site. For example, an adhesive particle described herein can be administered (e.g., injected) directly to a target tissue (e.g., cardiac infarct bed). Examples of adhesive moieties include, without limitation, PEG, positive charge, and self-assembly within tissue. In some cases, a targeting moiety can be conjugated to a particle described herein to direct delivery of a particle to a target tissue (e.g., cardiac infarct bed). Examples of targeting moieties include, without limitation, antigens, tissue targeting peptides, small molecules, and cell surface molecules. For example, an antibody can be used to target surface proteins on a cell. In some cases, the size of the particle can be used to direct delivery of a particle to a target tissue (e.g., cardiac infarct bed). Human capillaries measure about 5 μm to 10 μm in diameter. Thus, a particle described herein having a diameter of from about 0.3 μm to about 12 μm can enter a capillary via the bloodstream, but be limited from exiting the capillary, where the biologics and/or an expressed polypeptide can diffuse into the capillary bed of a tissue (e.g., heart, dermal, lung, solid tumor, brain, bone, ligament, connective tissue structures, kidney, liver, subcutaneous, and vascular tissue). Exemplary methods for delivery of one or more biologics using a biphasic particle described herein are shown in
A particle (e.g., an alginate gel) encapsulating one or more biologics described herein can be used to deliver the encapsulated biologic to a target tissue (e.g., cardiac infarct bed) in a temporally and/or spatially specific manner. For example, a biphasic particle encapsulating one or more biologics as described herein can be designed to confer a specific orientation of the particle within a blood vessel, to direct the biphasic particle into a capillary, and/or to confer specific release conditions of the encapsulated biologics. In cases where a biphasic particle has hydrophilic portions and hydrophobic portions on the particle surface, delivery of one or more encapsulated biologics can be controlled by the solvent present at the delivery site and/or the target site. In cases where a biphasic particle has differential density, the differential density can orient the particle in the blood flow to direct the particle in an appropriate orientation for delivery of one or more encapsulated biologics. For example, a dense side of a biphasic particle can lead the particle in the direction of blood flow within a blood vessel. In cases where a biphasic particle has a porous coating, delivery of one or more encapsulated biologics can be controlled by the differential porosity. For example, different amounts of porosity can help deliver particles within the blood vessel and alter the pattern of delivery. In cases where a biphasic particle has differential solubility, the differential solubility can orient the particle in the blood flow to direct the particle in an appropriate orientation for delivery of one or more encapsulated biologics. In cases where a biphasic particle has a tail extending from one portion of the particle surface, the tail can orient the particle within a blood vessel to direct the particle into a capillary. For example, a biphasic particle can be designed to have a tail to orient the particle within a blood vessel and direct the particle into a blood vessel (e.g., a capillary) where the encapsulated biologic can be delivered.
BiologicsAny appropriate biologic can be encapsulated within a particle described herein for delivery to a tissue. Examples of biologics that can be encapsulated within a particle described herein include, without limitation, nucleotides, polypeptides, small molecules, microvesicles, exosomes, extracellular vesicles, engineered cells, or combinations thereof. In some cases, a biologic can be a purified biologic (e.g., purified microvesicles or exosomes).
A particle (e.g., an alginate gel) described herein can be used to encapsulate one or more polypeptides. In some cases, a particle described herein can be used to encapsulate one or more polypeptides useful to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, a particle encapsulating a biologic described herein can encapsulate one or more polypeptides useful for regenerating cardiac function and/or tissue or a nucleotide that encodes such a polypeptide. Examples of polypeptides useful for regenerating cardiac function and/or tissue include, without limitation, antibodies having the ability to neutralize tumor necrosis factor (TNF; e.g., TNF-α) activity, antibodies having the ability to neutralize mitochondrial complex-1 activity, and resolvin-D1 agonists.
A particle (e.g., an alginate gel) described herein can be used to encapsulate one or more nucleotides. Examples of nucleotides that can be encapsulated within a particle include, without limitation, mRNAs, inhibitory RNAs (e.g., antisense RNAs, microRNAs (miRNAs), small interfering RNAs (siRNAs), short hairpin RNAs (shRNAs), and agomiRs), antagomiRs, modified mRNAs, loop-engineered modified mRNAs (see, e.g.,
In some cases, a particle (e.g., an alginate gel) described herein can be used to encapsulate one or more mRNAs useful to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, a particle encapsulating a biologic described herein can encapsulate one or more mRNAs encoding a polypeptide useful for regenerating cardiac function and/or tissue can be encapsulated within a particle described herein. Examples of polypeptides that can be useful for regenerating cardiac function and/or tissue include, without limitation, TNF-α, mitochondrial complex-1, resolvin-D1, NAP-2, TGF-α, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, CD80/86, polypeptides described in WO 2015/034897, or an antibody directed against any of the foregoing polypeptides. For example, a human Nap-2 polypeptide can have the amino acid sequence set forth in, for example, National Center for Biotechnology Information (NCBI) Accession No. NP_002695.1 (GI No. 5473) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_002704 (GI No. 5473). In some cases, a human TGF-α polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_003227.1 (GI No. 7039) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_003236 (GI No. 7039). In some cases, a human ErBb3 polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001005915.1 or NP_001973.2 (GI No. 2065) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001005915.1 or NM_001982.3 (GI No. 2065). For example, a human VEGF can have the amino acids set forth in NCBI Accession Nos. AAA35789.1 (GI: 181971), CAA44447.1 (GI: 37659), AAA36804.1 (GI: 340215), or AAK95847.1 (GI: 15422109), and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. AH001553.1 (GI: 340214). For example, a human IGF-1 can have the amino acid sequence set forth in NCBI Accession No. CAA01954.1 (GI: 1247519) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. A29117.1 (GI: 1247518). For example, a human FGF-2 can have the amino acid sequence set forth in NCBI Accession No. NP_001997.5 (GI: 153285461) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_002006.4 (GI: 153285460). For example, a human PDGF can have the amino acid sequence set forth in NCBI Accession No. AAA60552.1 (GI: 338209) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. AH002986.1 (GI: 338208). For example, a human IL-2 can have the amino acid sequence set forth in NCBI Accession No. AAB46883.1 (GI: 1836111) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. 577834.1 (GI: 999000). For example, a human CD19 can have the amino acid sequence set forth in NCBI Accession No. AAA69966.1 (GI: 901823) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. M84371.1 (GI: 901822). For example, a human CD20 can have the amino acid sequence set forth in NCBI Accession No. CBG76695.1 (GI: 285310157) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. AH003353.1 (GI: 1199857). For example, a human CD80 can have the amino acid sequence set forth in NCBI Accession No. NP_005182.1 (GI: 4885123) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_005191.3 (GI: 113722122), and a human CD86 can have the amino acid sequence set forth in NCBI Accession No. AAB03814.1 (GI: 439839) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. CR541844.1 (GI: 49456642). For example, a polypeptide that can be useful for regenerating cardiac function and/or tissue can be an antibody directed against TNF-α, mitochondrial complex-1, or resolvin-D1. In some cases, a particle encapsulating a biologic described herein can encapsulate one or more mRNAs encoding NAP-2 and/or TGF-α.
In some cases, a particle (e.g., an alginate gel) described herein can be used to encapsulate one or more inhibitory RNAs useful to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, a particle described herein can encapsulate one or more inhibitory RNAs inhibiting and/or reducing expression of one or more of the following polypeptides: eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, MMP-3, and polypeptides described in WO 2015/034897. For example, a human eotaxin-3 polypeptide can have an amino acid sequence set forth in, for example, NCBI Accession No: No. NP_006063.1 (GI No. 10344) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_006072 (GI No. 10344). In some cases, a human cathepsin-S can have the amino acid sequence set forth in NCBI Accession No. NP_004070.3 (GI No. 1520) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_004079.4 (GI No. 1520). In some cases, a human DK-1 can have the amino acid sequence set forth in NCBI Accession No. NP_036374.1 (GI No. 22943) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_012242 (GI No. 22943). In some cases, a human follistatin can have then amino acid sequence set forth in NCBI Accession No. NP_037541.1 (GI No. 10468) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_013409.2 (GI No. 10468). In some cases, a human ST-2 can have the amino acid sequence set forth in NCBI Accession No. BAA02233 (GI No. 6761) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No D12763.1 (GI No 6761). In some cases, a human GRO-α polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001502.1 (GI No. 2919) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001511 (GI No. 2919). In some cases, a human IL-21 can have the amino acid sequence set forth in NCBI Accession No. NP_068575.1 (GI No. 59067) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_021803 (GI No. 59067). In some cases, a human NOV polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_002505.1 (GI No. 4856) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_002514 (GI No. 4856). In some cases, a human transferrin polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001054.1 (GI No. 7018) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001063.3 (GI No. 7018). In some cases, a human TIMP-2 polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_003246.1 (GI No. 7077) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_003255.4 (GI No. 7077). In some cases, a human TNFαRI polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001056.1 (GI No. 7132) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001065 (GI No. 7132). In some cases, a human TNFαRII polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001057.1 (GI No. 7133) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001066 (GI No. 7133). In some cases, a human angiostatin polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_000292 (GI No. 5340) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_000301 (GI No. 5340). In some cases, a human CCL25 polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_005615.2 (GI No. 6370) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_005624 (GI No. 6370). In some cases, a human ANGPTL4 polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_001034756.1 or NP_647475.1 (GI No. 51129) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_001039667.1 or NM_139314.1 (GI No. 51129). In some cases, a human MMP-3 polypeptide can have the amino acid sequence set forth in NCBI Accession No. NP_002413.1 (GI No. 4314) and can be encoded by the nucleic acid sequence set forth in NCBI Accession No. NM_002422 (GI No. 4314).
In some cases, a particle (e.g., an alginate gel) described herein can be used to encapsulate one or more nucleotides that modulate (e.g., mimic or inhibit) microRNAs involved in cardiac regenerative potency. For example, a particle described herein can be used to encapsulate one or more agomiRs that mimic one or more miRNAs to augment cardiac regenerative potency. For example, a particle described herein can be used to encapsulate one or more antagomiRs that inhibit one or more miRNAs to augment cardiac regenerative potency. Examples of miRNAs involved in cardiac regenerative potency include, without limitation, miR-127, miR-708, miR-22-3p, miR-411, miR-27a, miR-29a, miR-148a, miR-199a, miR-143, miR-21, miR-23a-5p, miR-23a, miR-146b-5p, miR-146b, miR-146b-3p, miR-2682-3p, miR-2682, miR-4443, miR-4443, miR-4521, miR-4521, miR-2682-5p, miR-2682, miR-137.miR-137, miR-549.miR-549, miR-335-3p, miR-335, miR-181c-5p, miR-181c, miR-224-5p, miR-224, miR-3928, miR-3928, miR-324-5p, miR-324, miR-548h-5p, miR-548h-1, miR-548h-5p, miR-548h-2, miR-548h-5p, miR-548h-3, miR-548h-5p, miR-548h-4, miR-548h-5p, miR-548h-5, miR-4725-3p, miR-4725, miR-92a-3p, miR-92a-1, miR-92a-3p, miR-92a-2, miR-134, miR-134, miR-432-5p, miR-432, miR-651, miR-651, miR-181a-5p, miR-181a-1, miR-181a-5p, miR-181a-2, miR-27a-5p, miR-27a, miR-3940-3p, miR-3940, miR-3129-3p, miR-3129, miR-146b-3p, miR-146b, miR-940, miR-940, miR-484, miR-484, miR-193b-3p, miR-193b, miR-651, miR-651, miR-15b-3p, miR-15b, miR-576-5p, miR-576, miR-377-5p, miR-377, miR-1306-5p, miR-1306, miR-138-5p, miR-138-1, miR-337-5p, miR-337, miR-135b-5p, miR-135b, miR-16-2-3p, miR-16-2, miR-376c.miR-376c, miR-136-5p, miR-136, let-7b-5p, let-7b, miR-3′7′7-3p, miR-377, miR-1273g-3p, miR-1273g, miR-34c-3p, miR-34c, miR-485-5p, miR-485, miR-370.miR-370, let-7f-1-3p, let-7f-1, miR-3679-5p, miR-3679, miR-20a-5p, miR-20a, miR-585.miR-585, miR-3934, miR-3934, miR-127-3p, miR-127, miR-424-3p, miR-424, miR-24-2-5p, miR-24-2, miR-130b-5p, miR-130b, miR-138-5p, miR-138-2, miR-769-3p, miR-769, miR-1306-3p, miR-1306, miR-625-3p, miR-625, miR-193a-3p, miR-193a, miR-664-5p, miR-664, miR-5096.miR-5096, let-7a-3p, let-7a-1, let-7a-3p, let-7a-3, miR-15b-5p, miR-15b, miR-18a-5p, miR-18a, let-7e-3p, let-7e, miR-1287.miR-1287, miR-181c-3p, miR-181c, miR-3653, miR-3653, miR-15b-5p, miR-15b, miR-1, miR-1-1, miR-106a-5p, miR-106a, miR-3909.miR-3909, miR-1294.miR-1294, miR-1278, miR-1278, miR-629-3p, miR-629, miR-340-3p, miR-340, miR-200c-3p, miR-200c, miR-22-3p, miR-22, miR-128, miR-128-2, miR-382-5p, miR-382, miR-671-5p, miR-671, miR-27b-5p, miR-27b, miR-335-5p, miR-335, miR-26a-2-3p, miR-26a-2, miR-376b.miR-376b, miR-378a-5p, miR-378a, miR-1255a, miR-1255a, miR-491-5p, miR-491, miR-590-3p, miR-590, miR-32-3p, miR-32, miR-766-3p, miR-766, miR-30c-2-3p, miR-30c-2, miR-128.miR-128-1, miR-365b-5p, miR-365b, miR-132-5p, miR-132, miR-151b.miR-151b, miR-654-5p, miR-654, miR-374b-5p, miR-374b, miR-376a-3p, miR-376a-1, miR-376a-3p, miR-376a-2, miR-149-5p, miR-149, miR-4792.miR-4792, miR-1.miR-1-2, miR-195-3p, miR-195, miR-23b-3p, miR-23b, miR-127-5p, miR-127, miR-574-5p, miR-574, miR-454-3p, miR-454, miR-146a-5p, miR-146a, miR-7-1-3p, miR-7-1, miR-326.miR-326, miR-301a-5p, miR-301a, miR-31′73-5p, miR-3173, miR-450a-5p, miR-450a-1, miR-7-5p, miR-7-1, miR-7-5p, miR-7-3, miR-450a-5p, miR-450a-2, miR-1291, miR-1291, miR-7-5p, miR-7-2, and miR-17-5p, miR-17.
Nucleotides (e.g., RNA) encapsulated within a particle described herein can be modified nucleotides. In some cases, nucleotides can be modified for increased stability. For example, one or more uracil residues of an RNA described herein can be replace with a modified uracil residue. Examples of modified uracil residues include, without limitation, pseudouridine (T), dihydrouridine (D), and dideoxyuracil. An mRNA may be modified to form a biofunctionalized microencapsulated modified mRNA (M3RNA), which are described in more detail below.
A particle (e.g., an alginate gel) described herein can be used to encapsulate other molecules in addition to or in place of a biologic. In some cases, a particle (e.g., an alginate gel) described herein can be used to encapsulate one or more small molecules. For example, a particle described herein can be used to encapsulate one or more small molecules useful to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, a particle described herein can encapsulate one or more small molecules useful for regenerating cardiac function and/or tissue. Examples of small molecules useful for regenerating cardiac function and/or tissue include, without limitation, lipopolysaccharides, tumor necrosis factor (e.g., TNF-α) antagonists, mitochondrial complex-1 antagonists, and resolvin-D1 agonists. In some cases, a particle (e.g., an alginate gel) described herein can be used to encapsulate one or more microvesicles and/or exosomes. In some cases, a particle described herein can be used to encapsulate one or more microvesicles and/or exosomes useful to treat a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, a particle described herein can encapsulate one or more microvesicles and/or exosomes useful for regenerating cardiac function and/or tissue. Examples of microvesicles and exosomes useful for regenerating cardiac function and/or tissue include, without limitation, microvesicles and exosomes isolated from plasma, blood-derived products, and cultured stem cells.
A particle (e.g., an alginate gel) described herein also can include one or more detectable labels. A detectable label can be incorporated into the particle or encapsulated within the particle. Examples of detectable molecules include, without limitation, bioluminescent label (e.g., luciferase), fluorescent molecules (e.g., GFP and mCherry), and radionuclide molecules. In some cases, an mRNA expressing a detectable label is encapsulated within a particle such that temporal and/or spatial delivery of the encapsulated RNA can be monitored in a mammal.
A particle (e.g., an alginate gel) described herein also can include one or more additional therapeutic molecules. A therapeutic molecule can be conjugated to a particle, embedded within a particle, encapsulated within a particle, or any combination thereof. Examples of therapeutic agents include, without limitation, stem cells (e.g., mesenchymal stem cells, cardiac stem cells, and bone marrow), pharmaceuticals (e.g., statins, analgesics, chemotherapeutics, beta blockers, antibiotics, and nutrients (e.g., carbohydrates, fats, vitamins, and minerals).
In some cases, a particle (e.g., an alginate gel) encapsulating one or more biologics described herein can be used to encapsulate one or more nucleotides useful for treating other diseases and/or conditions.
Microencapsulated Modified mRNA (M3RNA)
M3RNA is a unique platform by which to induce rapid expression of encoded genes into a broad array of tissues. In the context of the M3RNA platform, M3RNA refers to modified microencapsulated mRNA; naked modified RNA (unencapsulated) is referred to as M2RNA. M3RNA is well suited for generating antibodies against new infectious threats. Intrinsic to this technological platform is the ability to rapidly scale within a short timeframe and simultaneously deliver multiple gene constructs. Due to the use of mRNA as the driving biologics within this platform, there is no integrative or mutation risk with therapy. Furthermore, unlike AAV and other viral gene-delivery technologies, the M3RNA platform avoids risk of immune reaction to the delivery system allowing its repetitive use with different constructs. M3RNA can be readily evolved into an M3RNA-Ig delivery system allowing efficient, rapid and sustained expression of antibodies against putative pathogens following delivery.
M3RNA has been tested to deliver several reporter and therapeutic gene constructs in both in vitro and in vivo models. Further, M3RNA can accommodate multi-gene therapeutic capability. M3RNA can simultaneously deliver, for example, several cardioregenerative genes in the setting of acute myocardial infarction. Specific to the transformation of M3RNA towards an M3RNA-Ig platform, is the demonstration of simultaneous delivery of reporter genes that emulate the size of IgG heavy and light chains in the form of GFP/mCherry mRNA (720 bp) and Firefly Luciferase (FLuc) mRNA (1653 bp). The system has been scaled to a three-gene delivery platform in vivo demonstrating similar penetrance for all reporter genes tested. The microencapsulated modified messenger RNA achieves rapid and robust protein expression within multiple cell lines and primary cells (human dermal fibroblasts, human cardiac fibroblasts, HEK293 cells, HL-1 cardiomyocytes, HUVAC cells, neonatal rat cardiomyocytes, and neonatal rat skeletal muscle cells). Furthermore, microencapsulating M3RNA using, for example, PEGylated charged nanoparticles induce rapid (within two hours) in vivo expression following direct injection into multiple organ systems (including both skeletal and cardiac muscle) in murine and porcine models.
Kinetics of M2RNA (modified mCherry mRNA) transfected into HEK293 (human embryonic kidney) cells resulted in mCherry protein expression in as early as two hours. Daily quantification of expression yielded fluorescence images for HEK293 cells at indicated time periods are shown in
The M3RNA platform is compatible with “hard-to-transfect” primary cell phenotypes such as, for example, neonatal rat cardiomyocytes. Neonatal primary cardiomyocytes were isolated and plated yielding synchronous beating pattern of cardiomyocytes in the dishes. Cardiomyocytes were transfected with mCherry M3RNA and fluorescence images were acquired starting at four hours post-transfection for six days days. Representative images for multiple time periods are shown in
The M3RNA platform also is compatible with intramuscular delivery, providing high transfection efficiency comparable with results obtained with primary cardiomyocyte cultures (
Microencapsulation of modified messenger RNA within a PEGylated cation-based micro particle system provides an exemplary platform by which to deliver M3RNA in vivo. Reporter genes including mCherry (720 bp), GFP (720 bp) mRNA, and Firefly Luciferase (FLuc) mRNA (1653 bp) were used in the in vivo setting. FLuc provided an added dimension to the analysis as the kinetics of protein expression in live animals could be prospectively documented. Using Luciferin to excite transfection areas provided an exact approach to decipher the localization of the M3RNA signal following delivery. Following optimization using a subcutaneous route, the M3RNA platform was tested in a broad array of tissues including intrahepatic, intrarenal, intraocular, intramuscular and intramyocardial delivery (
Within the heart, rapid FLuc expression following direct myocardial injections of FLuc M3RNA into the anterior left ventricle was quantified at different time points, revealing rapid induction of gene expression sustained over a three-day observation period (
The M3RNA technology can be evolved to achieve a delivery platform for rapid creation of highly potent therapeutics. For example, biofunctionalized M3RNA can form the foundation of an M3RNA-Ig Delivery System (MIDS) capable of rapidly integrating new genetic sequences to target novel pathogens (e.g., viral pathogen such as, for example, Zika virus and H7N9).
Compatibility of the M3RNA platform for the gene length of IgG heavy and light chain has been confirmed with the concomitant use of FLuc and fluorescent reporter gene, showing simultaneous induction of up to three genes within cardiac muscle tissue in vivo. Rapid and sustainable expression of genes encoded in the M3RNA-Ig vector can be enhanced using specialized design of the 5′ and 3′ UTR of the RNA molecule. Design of the M3RNA-Ig vector can involve consideration of one or more of the following: (1) whether to join the heavy and light chain genes on a single transcript with a P2A ribosomal skipping sequence versus synthesis as separate transcripts; (2) the length/introduction of the 3′poly(A) tail; (3) the type of 5′m7G cap; (4) selection of modified nucleotides; (5) IRES and pseudoknot modification of the 5′ and 3′ UTR, respectively, to diminish rate of degradation; and/or (6) nanoparticle-mediated microencapsulation to identify an appropriate stoichiometry for in vivo skeletal muscle delivery.
In some embodiments, the heavy and light chains can be synthesized on two separate transcripts. This approach allows rapid parallel work to incorporate the VL/VH antigen binding domains within a multicloning site (
mRNAs synthesized with poly(A) tail of 300 or more nucleotides have significant longer half-life and superior translational properties. In some embodiments, therefore, the vector can include a suitable promoter (e.g., T7), the heavy chain and light chain coding regions, and 300 nucleotide poly(T) tract will serve as the backbone template for mRNA transcription. Vectors can be designed as two separate versions to accommodate large variances in the C-regions of new antibodies identified. The initial design can assume an unchanging C-region in prospective antibodies identified. Accordingly, the multi-cloning site in the heavy chain and light chain vectors can allow rapid parallel introduction of the V sequence into this region and initiation of the M3RNA-Ig manufacturing process. Conversely, in certain cases, a varied Ig backbone may suggest adjustment also to the C regions of the parallel vector systems. As such, to ensure the capability for rapid response, additional vectors engineered with multi-cloning sites allowing for insertion of the entirety of the heavy and light chains can be designed.
The mRNA CAP mediates efficiency of the expression of the gene product. In some embodiments, M3RNA-Ig may be generated using CAP-1 as an approach to avoid any innate immune responses that may be mediated using CAP-0. A design including CAP-1 can include post-transcriptional modifications using a Vaccinia Capping System followed by a CAP 2′ O-Methyltransferase. However, a CAP-dependent approach can involve interaction of the poly(A) binding protein (PABP), which can add significant length to the construct and thereby limit creativity at the 3′ site to further limit RNA degradation (
An M3RNA system can limit undesirable side effects of mRNA transfection and/or slow degradation of the M3RNA by introducing modified nucleotides such as, for example, 5′-methylcytidine in place of cytosine or pseudouridine (T), dihydrouridine (D), or dideoxyuracil in place of uracil. Modified NTPs are readily abundant as GMP starting material and can be rapidly introduced using standard RNA synthesis techniques, providing significant molecular and translational advantage following delivery.
Alternatively, another strategy for extending the life of an mRNA in the cytosol involves interfering with the nonsense-mediated decay pathway. In the canonical pathway, as the ribosome complex hits the gag stop region, the 30s/50s subunits disengage from the mRNA, thus rendering the 3′ UTR of the mRNA highly susceptible to a UPF-1 mediated decay (
Nanoparticles for Delivery of Encapsulated or Unencapsulated mRNAs
Design of efficient gene delivery vectors possessing the high transfection efficiencies and low cytotoxicity is one challenge for delivering modified mRNAs—e.g., M2RNA, M3RNA, or M3RNA-Ig) to cells, tissue, or organs. Nanoparticles represents an exemplary model viral vector-free approach to deliver modified mRNAs. Nanoparticles possess remarkable flexibility for gene delivery including tissue targeting, protect mRNA against nuclease degradation, improve M2RNA stability through ionic interactions between the negatively charged mRNA and positively charged nanoparticle surface, and increase transformation efficiency for safety. Nanoparticles are generally accepted for therapeutic applications. First, nanoparticles exist in the same size domains as proteins. Second, nanoparticles have large surface areas that can be easily modified using, for example, PEGylation (to increase blood circulation half-life), or a poloxamer, a poloxamine, or chitosan for efficient binding and delivery. Third, modified nanoparticles can have controllable absorption and release properties, particle size, and/or surface characteristics.
A wide variety of organic (lipid-based), inorganic, or hybrid materials are used to produce nanoparticles and are discussed in detail above. In some embodiments, cationic polymer nanoparticles are used to microencapsulate modified messenger RNA. Cationic polymers have positively charged groups in their backbone to interact with negatively charged mRNA-Ig molecules to form neutralized, nanometer-sized complexes.
Multiple metallic nanoparticles have been suggested to cause minimum cytotoxicity. In various embodiments, nanoparticles made of iron, silver, gold, or copper can be used, alone or in combination with other nanoparticles and/or other delivery technologies, for delivering mRNA-Ig molecules.
Nanoparticles may be surface modified to increase the efficiency of modified RNA molecules, whether M2RNA (or M2RNA-Ig) or M3RNA (or M3RNA-Ig). Nanoparticles may be modified to introduce, for example, either a biopolymer or PEGylation to increase blood circulation half-life. In some embodiments for the delivery of M3RNA-Ig to skeletal muscle, the surface of the nanoparticle may be modified to include a biopolymer. Suitable biopolymers include, for example, collagen, elastin, fibronectin, chitosan, dextran etc. In particular embodiments, the surface of the nanoparticle may be modified with chitosan. Chitosan exhibits a cationic polyelectrolyte nature and therefore provides a strong electrostatic interaction with negatively charged DNA or RNA molecules. Moreover, chitosan carries primary amine groups that makes it a biodegradable, biocompatible, and non-toxic biopolymer that provides protection against DNase or RNase degradation.
In alternative embodiments, the surface of the nanoparticles may be modified by PEGylation. The technique of covalently attaching the polyethylene glycol (PEG) to a given molecule, nanoparticle in this case, is a well-established method in targeted drug delivery systems. PEGylation involves the polymerization of multiple monomethoxy PEG (mPEG) that are represented as CH3O—(CH2—CH2O)n—CH2—CH2—OH. Introducing PEG molecules significantly increases the half-life of a nanoparticle due to its increased hydrophobicity, reduces glomerular filtration rate, and/or lowers immunogenicity due to masking of antigenic sites by forming protective hydrophilic shield. Suitable modifications include modifying the surface of the nanoparticles to possess 3000-4000 PEG molecules, which provides a suitable environment for the physical binding of DNA or RNA molecules.
Taken together, the combination of nanoparticles with PEG, chitosan, and M2RNA generate the M3RNA platform (
Beyond molecular design, another challenge facing delivery of biologics in muscle tissue is the physical barrier to efficient transfer of biologic payload due, at least in part, to the dense and contractile nature of muscle tissue. Four-dimensional modeling of delivery in tissue using Darcy's Law, a significant limitation has been identified at a level inherent to the design of the needle. By having a straight needle with an end hole, biologics delivery creates a dense pocket of material within skeletal muscle tissue that mimics an abscess. The dense pocket dramatically reduces local tissue uptake of the biologics and preferentially eliminates the biologic via lymphatic and capillary action to alleviate the pressure. Conversely, an adjusted needle design, shown in
This document also provides methods of using a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein. In some cases, a mammal at risk of experiencing a major adverse cardiac event (e.g., a mammal identified as being likely to experience a major adverse cardiac event as described herein) can be treated by administering a particle encapsulating one or more biologics described herein. For example, a mammal at risk of experiencing a major adverse cardiac event can be treated by administering a particle encapsulating mRNA encoding NAP-2, TGF-α, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, and/or CD80/86 to increase the level of NAP-2, TGF-α, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, and/or CD80/86 polypeptide expression. An increase in the level of one or more of these polypeptides can be used to reduce scar size and tissue remodeling and to improve cardiac function. For example, a mammal at risk of experiencing a major adverse cardiac event can be treated by administering a particle encapsulating an inhibitory RNA targeting eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, and/or MMP-3 to decrease the level of eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, and/or MMP-3 polypeptide expression. A decrease in the level of one or more of these polypeptides can be used to reduce scar size and tissue remodeling and to improve cardiac function.
Any type of mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., a mammal who underwent PCI for STEMI) can be treated with using particle-mediated delivery of one or more biologics described herein. For example, humans and other primates such as monkeys experiencing a major adverse cardiac event and/or at risk of experiencing a major adverse cardiac event can be treated with biologics as described herein. In some cases, dogs, cats, horses, cows, pigs, sheep, rabbits, mice, and rats can be treated with biologics as described herein.
Any appropriate method can be used to identify a mammal experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or a mammal at risk of experiencing a major adverse cardiac event (e.g., patients who underwent PCI for STEMI). For example, the methods of identifying a mammal at risk of experiencing a major adverse cardiac event described elsewhere (e.g., WO 2015/034897) can be used.
Once identified as experiencing a major adverse cardiac event (e.g., acute myocardial infarction) and/or being at risk of experiencing a major adverse cardiac event, the patient can be administered or instructed to self-administer one or more particles encapsulating a molecule (e.g., a biologic) as described herein.
When treating mammal experiencing a major adverse cardiac event or at risk of experiencing a major adverse cardiac event as described herein, the major adverse cardiac event can be any major adverse cardiac event. Examples of major adverse cardiac events include, without limitation, myocardial infarction (e.g., acute myocardial infarction), heart failure, recurrent myocardial infarction, repeat hospitalization for cardiac-related events, and ischemic heart disease. In some embodiments, the major adverse cardiac event treated as described herein can be myocardial infarction, such as acute myocardial infarction.
In some cases, particle-mediated delivery of one or more molecules (e.g., biologics) to a mammal as described herein can be used to improve cardiac function. Examples of improved cardiac function include, without limitation, increased survivorship, reduced hospitalization, symptom-free tolerance of physical activity, improved global physical fitness, improved cardiac ejection fraction, improved cardiac output, improved stroke volume, improved cardiac mass index, and reduced scar size.
In some cases, particle-mediated delivery of one or more biologics (e.g., mRNA) to a mammal as described herein can be used to increase expression of one or more (e.g., one, two, three, or more) polypeptides useful for regenerating cardiac function and/or tissue. Examples of polypeptides that can be useful for regenerating cardiac function and/or tissue include, without limitation, NAP-2, TGF-α, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, CD80/86, and polypeptides described in WO 2015/034897. An increase in the level of one or more of these polypeptides can be used to reduce scar size and tissue remodeling and/or improve cardiac function. Methods for increasing expression of a polypeptide useful for regenerating cardiac function and/or tissue in cells (e.g., cardiomyocytes) can include contacting the cells with one or more particles encapsulating, for example, an mRNA encoding the polypeptide. One or more particles encapsulating an mRNA encoding the polypeptide can be contacted with the cells by any appropriate method. The term “increased expression” as used herein with respect to the level of a polypeptide is any level that is greater than (e.g., at least about 10, 15, 20, or 25 percent greater than) a reference level for that polypeptide. The term “reference level” as used herein with respect to a polypeptide is the level of expression of that polypeptide typically observed by healthy humans or humans with a low risk of experiencing a major adverse cardiac event. For example, levels of NAP-2, TGF-α, and ErBb3 expression with respect to healthy humans or humans with a low risk of experiencing a major adverse cardiac event can be as described elsewhere (e.g., WO 2015/034897). In some cases, particle-mediated delivery of one or more biologics (e.g., mRNA) to a mammal as described herein can be used to increase expression of NAP-2 and/or TGF-α.
In some cases, particle-mediated delivery of one or more biologics (e.g., inhibitory RNA) to a mammal described herein can be used to decrease expression of one or more (e.g., one, two, three, four, five, six, seven, eight, nine, ten, or more) of the following polypeptides: eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, MMP-3, and polypeptides described in WO 2015/034897. A decrease in the expression level of one or more of these polypeptides can be used to reduce scar size and tissue remodeling and/or improve cardiac function. Methods for decreasing expression of one or more of eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, and MMP-3 in cells can include contacting the cells (e.g., cardiomyocytes) with one or more particles encapsulating, for example, an inhibitory RNA. One or more particles encapsulating an inhibitory RNA can be contacted with the cells by any appropriate method. For example, in humans, a particle encapsulating an inhibitory RNA described herein can be used to decrease expression of a human eotaxin-3, a human cathepsin-S, a human DK-1, a human follistatin, a human ST-2, a human GRO-α, a human IL-21, a human NOV, a human transferrin, a human TIMP-2, a human TNFαRI, a human TNFαRII, a human angiostatin, a human CCL25, a human ANGPTL4, a human MMP-3, or any combination thereof. The term “decreased expression” as used herein with respect to the level of a polypeptide (e.g., eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, or MMP-3) is any level that is lower than (e.g., at least about 10 percent, at least about 15 percent, at least about 20 percent, or at least about 25 percent lower than) a reference level for that polypeptide. The term “reference level” as used herein with respect to a eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-α, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, or MMP-3 polypeptide is the level of expression of that polypeptide typically observed by healthy humans or humans with a low risk of experiencing a major adverse cardiac event. Levels of eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-a, IL-21, NOV, transferrin, TIMP-2, TNFαRI, TNFαRII, angiostatin, CCL25, ANGPTL4, and MMP-3 expression with respect to healthy humans or humans with a low risk of experiencing a major adverse cardiac event can be as described elsewhere (e.g., WO 2015/034897).
A particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be administered to a mammal experiencing a major adverse cardiac event or likely to experience a major adverse cardiac event as a combination therapy with one or more additional agents/therapies used to treat a major adverse cardiac event. For example, a combination therapy used to treat a mammal identified as being likely to experience a major adverse cardiac event as described herein can include administering an alginate gel encapsulating one or more biologics described herein and treating with aggressive pharmacotherapy (e.g., beta-adrenoceptor blockade, angiotensin converting enzyme inhibitors, aldosterone antagonism treatments, and/or antiplatelet agents), hemodynamic support (e.g., intra-aortic balloon pump and/or mechanical augmentation of cardiac output), surgical intervention (e.g., coronary bypass grafting or left ventricular assist device placement), and/or device-based intervention (e.g., resychronization therapy or implantable cardiac defibrillators).
In embodiments where a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein is used in combination with additional agents/therapies used to treat a major adverse cardiac event, the one or more additional agents can be administered at the same time or independently. For example, an alginate gel encapsulating one or more biologics described herein can be administered first, and the one or more additional agents administered second, or vice versa. In embodiments where a particle (e.g., an alginate gel) encapsulating one or more biologics described herein is used in combination with one or more additional therapies used to treat a major adverse cardiac event, the one or more additional therapies can be performed at the same time or independently of the administration of one or more particles encapsulating one or more biologics described herein. For example, the one or more alginate gels encapsulating one or more biologics described herein can be administered before, during, or after the one or more additional therapies are performed.
In some cases, a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be used to treat numerous other diseases and/or conditions including, without limitation, a hematologic disorder or hematologic malignancy (e.g., lymphoma, lymphocytic leukemia, myeloma, myelogenous leukemia (e.g., acute myelogenous leukemia and chronic myelogenous leukemia), myelodysplastic syndromes, and myeloproliferative diseases), a musculoskeletal disorder (e.g., carpal tunnel syndrome, epidondylitis, tendinitis, back pain, tension neck syndrome, and hand-arm vibration syndrome), a pulmonary condition (e.g., asthma, chronic obstructive pulmonary disease, chronic bronchitis, emphysema, acute bronchitis, cystic fibrosis, pneumonia, tuberculosis, emphysema, pulmonary edema, acute respiratory distress syndrome, pneumoconiosis, and interstitial lung disease), a gastrointestinal, colorectal, anal-sphincter and/or pelvic organ disease (e.g., enterocolitis, infectious diarrhea, mesenteric ischaemia, inflammatory bowel disease, and pelvic inflammatory disease), a neurologic, spinal cord and/or intracranial disease (e.g., neural tube defects, cephalic disorders, raised or decreased intracranial pressure, meningitis, neuropathies, motor neuron diseases, demyelinating neuropathies, and nerve injuries), a dermatologic disorder (e.g., eczema (e.g., atopic dermatitis), warts, acne, and roseola), chronic inflammatory conditions (e.g., asthma, chronic peptic ulcer, tuberculosis, rheumatoid arthritis, chronic periodontitis, ulcerative colitis and crohn's disease, chronic sinusitis, chronic active hepatitis), and/or genetic defects.
In some cases, a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be formulated into a pharmaceutically acceptable composition for administration to a mammal experiencing a major cardiac event or at risk of experiencing a major cardiac event. For example, a therapeutically effective amount of an alginate gel encapsulating a biologic described herein can be formulated together with one or more pharmaceutically acceptable carriers (additives) and/or diluents. A pharmaceutical composition can be formulated for administration in solid or liquid form including, without limitation, sterile solutions, suspensions, sustained-release formulations, tablets, capsules, pills, powders, and granules.
Pharmaceutically acceptable carriers, fillers, and vehicles that may be used in a pharmaceutical composition described herein include, without limitation, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat.
A pharmaceutical composition containing a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be designed for oral, parenteral (including subcutaneous, intraarterial, intramuscular, intravenous, intracoronary, intradermal, or topical), or inhaled administration. When being administered orally, a pharmaceutical composition containing a particle (e.g., an alginate gel) encapsulating one or more biologics described herein can be in the form of a pill, tablet, or capsule. Compositions suitable for parenteral administration include aqueous and non-aqueous sterile injection solutions that can contain anti-oxidants, buffers, bacteriostats, and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents. Compositions for inhalation can be delivered using, for example, an inhaler, a nebulizer, and/or a dry powder inhaler. The formulations can be presented in unit-dose or multi-dose containers, for example, sealed ampules and vials, and may be stored in a freeze dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example water for injections, immediately prior to use. Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules, and tablets.
A pharmaceutically acceptable composition including a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be administered locally or systemically. In some cases, a composition containing a particle encapsulating one or more biologics described herein can be administered systemically by venous or oral administration to, or inhalation by a mammal (e.g., a human). In some cases, a composition containing a particle encapsulating one or more biologics described herein can be administered locally by percutaneous, subcutaneous, intramuscular, or open surgical administration (e.g., injection) to a target tissue (e.g., cardiac infarct bed) of a mammal (e.g., a human), or by arterial administration to the vascular supply of a target tissue (e.g., cardiac infarct bed) of a mammal (e.g., a human). For example, arterial administration of an alginate gel encapsulating one or more biologics described herein to the vascular supply of the heart can be used to deliver the biologics to the cardiac infarct bed of a human.
Effective doses can vary depending on the severity of the major cardiac event, the route of administration, the age and general health condition of the subject, excipient usage, the possibility of co-usage with other therapeutic treatments such as use of other agents, and the judgment of the treating physician.
The frequency of administration can be any frequency that improves cardiac function without producing significant toxicity to the mammal. For example, the frequency of administration can be from about once a week to about three times a day, from about twice a month to about six times a day, or from about twice a week to about once a day. The frequency of administration can remain constant or can be variable during the duration of treatment. A course of treatment with a composition containing a particle (e.g., an alginate gel) encapsulating one or more biologics described herein can include rest periods. For example, a composition containing an alginate gel encapsulating one or more biologics described herein can be administered daily over a two-week period followed by a two week rest period, and such a regimen can be repeated multiple times. As with the effective amount, various factors can influence the actual frequency of administration used for a particular application. For example, the effective amount, duration of treatment, use of multiple treatment agents, route of administration, and severity of the major cardiac event may require an increase or decrease in administration frequency.
An effective duration for administering a composition containing a particle (e.g., an alginate gel) encapsulating one or more molecules (e.g., biologics) described herein can be any duration that improves cardiac function without producing significant toxicity to the mammal. For example, the effective duration can vary from several days to several weeks, months, or years. In some cases, the effective duration for the treatment of a major cardiac event can range in duration from about one month to about 10 years. Multiple factors can influence the actual effective duration used for a particular treatment. For example, an effective duration can vary with the frequency of administration, effective amount, use of multiple treatment agents, route of administration, and severity of the major cardiac event being treated.
In certain instances, a course of treatment and the cardiac function of the mammal being treated for a major cardiac event can be monitored. Any appropriate method can be used to monitor cardiac function. For example, cardiac function can be assessed using blood tests, electrocardiography (ECG/EKG), cardiac stress testing, coronary catheterization, echocardiogram, and/or intravascular ultrasound at different time points.
In the preceding description, particular embodiments may be described in isolation for clarity. Unless otherwise expressly specified that the features of a particular embodiment are incompatible with the features of another embodiment, certain embodiments can include a combination of compatible features described herein in connection with one or more embodiments.
For any method disclosed herein that includes discrete steps, the steps may be conducted in any feasible order. And, as appropriate, any combination of two or more steps may be conducted simultaneously.
The present invention is illustrated by the following examples. It is to be understood that the particular examples, materials, amounts, and procedures are to be interpreted broadly in accordance with the scope and spirit of the invention as set forth herein.
Examples Example 1: mRNA Expression in FibroblastsmCherry mRNA was transfected into human dermal fibroblasts and human cardiac fibroblasts. Light phase and fluorescent microscopy was used to evaluate mRNA expression at 4 hours, 2 days, and 5 days post transfection (
These results demonstrated that mRNA can be sustainably expressed in dermal and cardiac fibroblasts.
Example 2: mRNA Co-Expression in Epithelial CellsmCherry mRNA and EGFP mRNA were transfected into HEK293 cells. Multi-channel fluorescent microscopy was used to evaluate mRNA expression at 24 hours post transfection (
These results demonstrated that multiple mRNAs can be co-expressed.
Example 3: mRNA Expression in CardiomyocytesmCherry mRNA was transfected into HEK293 cells. Light phase and fluorescent microscopy was used to evaluate mRNA expression at 24 hours, 3 days, and 5 days post transfection (
These results demonstrated that mRNA can be sustainably expressed in cardiomyocytes.
Example 4: In Vivo Expression of Subcutaneous Liposome-Delivered mRNAMice were administered a solution of luciferase mRNA via hydrodynamic tail vein injection (
Mice were administered liposomes containing mCherry mRNA via subcutaneous injection. mCherry expression was evaluated using fluorescent microscopy (
These results demonstrated that liposome delivered mRNA can be sustainably expressed in vivo following subcutaneous administration.
Example 5: In Vivo Expression of Intracardiac Liposome-Delivered mRNAMice were administered liposomes containing luciferase mRNA via echo guided intracardiac injection (
These results demonstrated that liposome delivered mRNA can be sustainably expressed in vivo following intracardiac administration.
Example 6: In Vivo Expression of Open-Chest Intracardiac Liposome-Delivered mRNAMice were administered liposomes containing luciferase mRNA via open chest intracardiac injection. Luciferase expression was imaged using a Xenogen (IVIS) imaging system (
These results demonstrated that liposome delivered mRNA can be sustainably expressed in vivo following intracardiac administration.
Example 7: In Vivo Expression of Alginate-Delivered mRNAPigs were administered alginate gel containing mCherry mRNA using previous reported approaches. The amount of mCherry expression was evaluated after the administration (
Previous methods of using alginate delivery of mRNA resulted in sequestration of biologics within the polymerized product with no intramyocardial expression.
Example 8: In Vivo Expression of Alginate-Delivered mRNAPigs were administered a reduced volume of alginate gel containing mCherry mRNA. mCherry expression was evaluated using fluorescent microscopy.
Reduced alginate gel volume resulted in diffuse delivery of biologics and loss of the majority of signal (3.6 radiance efficiency;
Pigs were administered alginate gels having varied alginate/calcium concentrations containing mCherry mRNA. mCherry expression was evaluated using fluorescent microscopy.
Targeted delivery into the infarct bed with an alginate/calcium gel remaining liquid in blood and escaping into the infarcted capillary bed where it polymerized and delivered the biologics with high efficiency (localized radiance level >10 versus 3-4 in prior efforts;
These results demonstrated that alginate gel delivered mRNA can be targeted to infarcted capillary beds.
Example 10: In Vivo Expression of Open-Chest Intracardiac Alginate-Delivered mRNAMice were administered alginate gels having varied alginate/calcium concentrations containing mCherry mRNA. mCherry expression was evaluated using fluorescent microscopy.
Alginate gel delivery resulted in sustained release of mCherry mRNA (
These results demonstrated that alginate gel delivered mRNA can be sustainably expressed in vivo following delivery.
Claims
1. A method for improving cardiac function in a mammal, the method comprising:
- administering to the mammal a composition comprising a particle encapsulating an mRNA, the mRNA encoding a polypeptide useful for regenerating cardiac function or regenerating tissue, thereby improving cardiac function of the mammal.
2. The method of claim 1, wherein the polypeptide is NAP-2, TGF-α, ErBb3, VEGF, IGF-1, FGF-2, PDGF, IL-2, CD19, CD20, or CD80/86.
3. The method of claim 1, wherein the mammal is a human.
4. The method of claim 3, wherein the human has undergone percutaneous coronary intervention for ST-elevation myocardial infarction.
5. The method of claim 1, wherein the composition is administered to the mammal by arterial administration.
6. The method of claim 1, wherein the particle comprises alginate.
7. The method of claim 6, wherein the alginate is in the form of an alginate gel.
8. The method of claim 7, wherein the alginate gel comprises a calcium salt.
9. The method of claim 8, wherein the alginate gel has a ratio of alginate to calcium salt can be from about 2:1 to about 10:1.
10. The method of claim 1, wherein the particle is from about 5 μm to about 10 μm in diameter.
11. The method of claim 1, wherein the particle is a biphasic particle.
12. The method of claim 11, wherein the biphasic particle is a polarized particle.
13. The method of claim 11, wherein the biphasic particle comprises a tail.
14. The method of claim 1, wherein the method comprises administering the composition during a percutaneous coronary intervention.
15. The method of claim 1, where the particle further comprises a scaffold protein.
16. The method of claim 15, where the scaffold protein is selected from the group consisting of collagen I, collagen II, collagen III, collagen IV, fibrin, and gelatin.
17. The method of claim 1, where the particle further encapsulates a polypeptide.
18. The method of claim 17, where the polypeptide is an antibody having the ability to neutralize tumor necrosis factor activity, an antibody having the ability to neutralize mitochondrial complex-1 activity, or a resolvin-D1 agonist.
19. The method of claim 1, where the particle further encapsulates a lipopolysaccharide.
20. The method of claim 1, wherein the particle further encapsulates a microvesicle and/or exosome.
21. A method for improving cardiac function in a mammal, the method comprising: administering to the mammal composition comprising a particle encapsulating an inhibitory RNA, the inhibitory RNA reducing expression of a polypeptide in which reduced expression of the polypeptide improves cardiac function, thereby improving cardiac function of the mammal, wherein the polypeptide is eotaxin-3, cathepsin-S, DK-1, follistatin, ST-2, GRO-a, IL-21, NOV, transferrin, TIMP-2, TNFaRI, TNFaRII, angiostatin, CCL25, ANGPTL4, or MMP-3.
22. The method of claim 21, wherein the mammal is a human.
23. The method of claim 22, wherein the human has undergone percutaneous coronary intervention for ST-elevation myocardial infarction.
24. The method of claim 21, wherein the composition is administered to the mammal by arterial administration.
25. The method of claim 21, wherein the particle comprises alginate.
26. The method of claim 25, wherein the alginate is in the form of an alginate gel.
27. The method of claim 26, wherein the alginate gel comprises a calcium salt.
28. The method of claim 27, wherein the alginate gel has a ratio of alginate to calcium salt can be from about 2:1 to about 10:1.
29. The method of claim 21, wherein the particle is from about 5 μm to about 10 μm in diameter.
30. The method of claim 21, wherein the particle is a biphasic particle.
31. The method of claim 30, wherein the biphasic particle is a polarized particle.
32. The method of claim 30, wherein the biphasic particle comprises a tail.
33. The method of claim 21, wherein the method comprises administering the composition during a percutaneous coronary intervention.
34. The method of claim 21, where the particle further comprises a scaffold protein.
35. The method of claim 34, where the scaffold protein is selected from the group consisting of collagen I, collagen II, collagen III, collagen IV, fibrin, and gelatin.
36. The method of claim 21, where the particle further encapsulates a polypeptide.
37. The method of claim 36, where the polypeptide is selected from the group consisting of an antibody having the ability to neutralize tumor necrosis factor activity, an antibody having the ability to neutralize mitochondrial complex-1 activity, and a resolvin-D1 agonist.
38. The method of claim 21, where the particle further encapsulates a lipopolysaccharide.
39. The method of claim 21, wherein the particle further encapsulates a microvesicle and/or exosome.
40. A composition comprising:
- a particulate substrate;
- an mRNA attached to the particulate substrate, the mRNA comprising at least one modification to inhibit degradation of the mRNA when the mRNA is in cytosol of a cell, the mRNA encoding at least one therapeutic polypeptide.
41. The composition of claim 40, wherein the mRNA modification comprises a pseudoknot, an RNA stability element, or an artificial 3′ stem loop.
42. The composition of claim 40, wherein the particulate substrate comprises a surface modification.
43. The composition of claim 42, wherein the surface modification comprises a biocompatible polymer.
44. The composition of claim 43, wherein the biocompatible polymer comprises polyethylene glycol (PEG).
45. The composition of claim 44, wherein the biocompatible polymer comprises chitosan.
46. The composition of claim 40, wherein the particulate substrate comprises a nanoparticle.
47. The composition of claim 40, wherein the particulate substrate comprises a microparticle.
48. The composition of claim 40, wherein the particulate substrate comprises a plurality of nanoparticles.
49. The composition of claim 48, wherein the plurality of nanoparticles comprises:
- at least one nanoparticle comprising from a first material; and
- at least one nanoparticle comprising a second material.
50. The composition of claim 40, wherein the therapeutic polypeptide comprises:
- an immunoglobulin heavy chain; or
- an immunoglobulin light chain.
Type: Application
Filed: Nov 22, 2017
Publication Date: Sep 12, 2019
Inventors: Atta Behfar (Rochester, MN), Andre Terzic (Rochester, MN)
Application Number: 16/463,053
