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Modified HGP-30 heteroconjugates, compositions and methods of use
   
Document Number
US Patent 6287565
Issued Date
September 11, 2001
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Abstract
A heteroconjugate is formed by linking a T cell binding ligand (TCBL) such as Peptide J of .beta.-2 microglobulin to a modified HGP-30 antigentic peptide fragment of p17 gag peptide, such as, for example The heteroconjugate is effective in eliciting a THI directed immune response and provides a vaccine composition for treating or preventing AIDS.
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Number of Claims:
10
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Owner
Cel-Sci Corporation (Vienna, VA)
Published
September 11, 2001
Application Number
09/594,845
Filed
June 15, 2000
US Classification
424/188.1   424/185.1 424/186.1 424/187.1 424/196.11 514/12 514/13 530/324 530/327 530/826
Int'l Classification
C07K   14/435   (20060101)   C07K   14/74   (20060101)   C07K   14/16   (20060101)   C07K   14/005   (20060101)   C07K   16/08   (20060101)   C07K   16/10   (20060101)   A61K   39/00   (20060101)  
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Parent Case
CROSS-REFERENCE TO RELATED APPLICATIONS This application is a continuation of application Ser. No. 08/695,304, filed Aug. 8, 1996, now U.S. Pat. No. 6,103,239.
USPTO Field of Search
424/185.1   424/186.1   424/188.1   424/196.11   424/187.1   514/12   514/13   530/324   530/327   530/826  
Related Patents
7199216 - Peptide constructs for treating autoimmune and related diseases - Owned by Cel-Sci Corporation (Vienna, VA)

Conjugated peptides include a first peptide component which is an antigen associated with autoimmune disease, allergy, asthma or transplantation rejection and binds to an antigen-specific receptor on a T cell, and a second peptide component which corresponds to an "antigen presenting molecule", namely, a peptide binding to a T cell surface receptor, which would normally promote T cell activation when the first peptide is bound to its antigen-specific T cell receptor. However, in this invention, the second peptide component has an amino acid sequence which is a modification of an antigen presenting T cell binding peptide, such modification blocking or inhibiting the engagement of receptor sites on the T cell surface (other than the antigen-specific T cell receptor). As a result, T cell activation is prevented, and is directed through antigen-specific T cell receptor occupation, without T cell activation, leading to antigen-specific T cell anergy and cell death. Administration of the conjugated peptide to an animal will provide protection against disease associated with the first peptide component, resulting from the elimination of the T cells bearing the antigen-specific receptors for that anti genic peptide. The conjugated peptides of this invention provide antigen-specific protection without impairing the immune response to other antigens.

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