Patents by Inventor Marja Heiskala

Marja Heiskala has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 9222071
    Abstract: T cell responses are often diminished in humans with a compromised immune system. We have developed a method to isolate, stimulate and expand naïve cytotoxic T lymphocyte precursors (CTLp) to antigen-specific effectors, capable of lysing tumor cells in vivo. This ex vivo protocol produces fully functional effectors. Artificial antigen presenting cells (AAPCs; Drosophila melanogaster) transfected with human HLA class I and defined accessory molecules, are used to stimulate CD8+ T cells from both normal donors and cancer patients. The class I molecules expressed to a high density on the surface of the Drosophila cells are empty, allowing for efficient loading of multiple peptides that results in the generation of polyclonal responses recognizing tumor cells endogenously expressing the specific peptides. The responses generated are robust, antigen-specific and reproducible if the peptide epitope is a defined immunogen.
    Type: Grant
    Filed: January 16, 2008
    Date of Patent: December 29, 2015
    Assignee: Janssen Pharmaceuticals, Inc.
    Inventors: Ann Moriarty, Didier J. Leturcq, Juli Degraw, Michael R. Jackson, Per A. Peterson, Marja Heiskala
  • Publication number: 20090305418
    Abstract: T cell responses are often diminished in humans with a compromised immune system. We have developed a method to isolate, stimulate and expand naïve cytotoxic T lymphocyte precursors (CTLp) to antigen-specific effectors, capable of lysing tumor cells in vivo. This ex vivo protocol produces fully functional effectors. Artificial antigen presenting cells (AAPCs; Drosophila melanogaster) transfected with human HLA class I and defined accessory molecules, are used to stimulate CD8+ T cells from both normal donors and cancer patients. The class I molecules expressed to a high density on the surface of the Drosophila cells are empty, allowing for efficient loading of multiple peptides that results in the generation of polyclonal responses recognizing tumor cells endogenously expressing the specific peptides. The responses generated are robust, antigen-specific and reproducible if the peptide epitope is a defined immunogen.
    Type: Application
    Filed: January 16, 2008
    Publication date: December 10, 2009
    Inventors: Ann Moriarty, Didier J. Leturqc, Juli Degraw, Michael R. Jackson, Per A. Peterson, Marja Heiskala
  • Patent number: 7026127
    Abstract: Methods of detecting the presence of a tumor or a cancerous condition includes detecting the expression of RELP proteins, related polypeptides and proteins, or nucleic acid molecules indicative of such expression are presented. These methods include antibody-based assays and molecular diagnostic assays such as PCR-based methods.
    Type: Grant
    Filed: March 18, 2002
    Date of Patent: April 11, 2006
    Inventor: Marja Heiskala
  • Publication number: 20050164232
    Abstract: REG-Like proteins and purified and isolated nucleic acids relating to them are used in kits and methods for detecting cancers.
    Type: Application
    Filed: September 7, 2004
    Publication date: July 28, 2005
    Inventor: Marja Heiskala
  • Publication number: 20040167086
    Abstract: The present invention relates to at least one novel RELP Ig derived protein or specified portion or variant, including isolated nucleic acids that encode at least one RELP Ig derived protein or specified portion or variant, RELP Ig derived protein or specified portion or variants, vectors, host cells, transgenic animals or plants, and methods of making and using thereof, including therapeutic compositions, methods and devices.
    Type: Application
    Filed: March 14, 2002
    Publication date: August 26, 2004
    Inventor: Marja Heiskala
  • Publication number: 20030077248
    Abstract: T cell responses are often diminished in humans with a compromised immune system. We have developed a method to isolate, stimulate and expand naive cytotoxic T lymphocyte precursors (CTLp) to antigen-specific effectors, capable of lysing tumor cells in vivo. This ex vivo protocol produces fully functional effectors. Artificial antigen presenting cells (AAPCs; Drosophila melanogaster) transfected with human HLA class I and defined accessory molecules, are used to stimulate CD8+ T cells from both normal donors and cancer patients. The class I molecules expressed to a high density on the surface of the Drosophila cells are empty, allowing for efficient loading of multiple peptides that results in the generation of polyclonal responses recognizing tumor cells endogenously expressing the specific peptides. The responses generated are robust, antigen-specific and reproducible if the peptide epitope is a defined immunogen.
    Type: Application
    Filed: February 19, 2002
    Publication date: April 24, 2003
    Inventors: Ann Moriarty, Didier J. Leturqc, Juli Degraw, Michael R. Jackson, Per A. Peterson, Marja Heiskala