Abstract: The invention includes human .epsilon. chain transmembrane anchor peptide resulting from mRNA splicing other than the C.epsilon.4 exon, the .epsilon.m1 exon, and the .epsilon.m2 exon. Two new peptides in particular have been specifically identified. These novel peptides are not present in the conventional secreted (and circulating) IgE. These peptides provide antigenic sites for antibody binding. Thus, the invention further includes antibodies to such peptide segments, as well as such antibodies conjugated to cytotoxic agents, and their use in extracorporeal or in vivo therapy.
Abstract: Immunogenic compositions useful for the treatment or prevention of gastric or duodenal ulcer disease are disclosed. The immunogenic compositions effectively operate by inducing antibodies in a subject which selectively neutralize specific peptide gastric hormones and inhibit the binding of the hormones to physiological receptors thus limiting the secretion of stomach acid. Pharmaceutical compositions comprising effective amounts of the immunogenic compositions and methods of treatment using the compositions are also disclosed.
Type:
Grant
Filed:
January 24, 1989
Date of Patent:
June 11, 1991
Assignee:
Aphton Corporation
Inventors:
Philip C. Gevas, Stephen L. Karr, Jr., Stephen Grimes, Richard L. Littenberg
Abstract: A method for the solid phase synthesis of multi-sulfated peptides comprising coupling side-chain unprotected hydroxyamino acids to the peptide chain utilizing benzotriazol-1-yl-oxy-tris (dimethyl)-phosphonium hexafluorophosphate (BOP) as a coupling reagent.
Type:
Grant
Filed:
January 28, 1988
Date of Patent:
October 23, 1990
Assignee:
Hoffmann-La Roche Inc.
Inventors:
Arthur M. Felix, Alain Fournier, Waleed Danho
Abstract: Compounds and compositions comprising cyclic synthetic analogs of Atrial Natriuretic Peptides are provided, together with methods for their production and use as natriuretics, diuretics and/or vasodilators, or as intermediates for or modulators of such useful compounds or of native Atrial Natriuretic Peptides.
Type:
Grant
Filed:
March 29, 1988
Date of Patent:
June 19, 1990
Assignee:
California Biotechnology Inc.
Inventors:
John A. Lewicki, Robert M. Scarborough, Lorin K. Johnson
Abstract: Disclosed herein is a physiologically-active peptide represented by the following general formula (I): ##STR1## wherein X means H or H-Asp-Ser-Gly- and Y denotes -Asn-Val-Leu-Arg-Arg-Tyr-OH, -Asn-Val-Leu-Arg-Arg-OH, -Asn-Val-Leu-Arg-Tyr-OH, -Asn-Val-Leu-Arg-OH, -Asn-Val-Leu-OH or -Asn-Ser-Phe-Arg-Tyr-OH, or a salt thereof.
Type:
Grant
Filed:
June 17, 1988
Date of Patent:
February 27, 1990
Assignees:
Daiichi Pure Chemicals Co., Ltd., Hisayuki Matsuo