Literature DB >> 11519731

TCR peptide therapy in human autoimmune diseases.

A A Vandenbark1, E Morgan, R Bartholomew, D Bourdette, R Whitham, D Carlo, D Gold, G Hashim, H Offner.   

Abstract

Inflammatory Th1 cells reacting to tissue/myelin derived antigens likely contribute to the pathogenesis of diseases such as multiple sclerosis (MS), rheumatoid arthritis (RA), and psoriasis. One regulatory mechanism that may be useful for treating autoimmune diseases involves an innate second set of Th2 cells specific for portions of the T cell receptor of clonally expanded pathogenic Th1 cells. These Th2 cells are programmed to respond to internally modified V region peptides from the T cell receptor (TCR) that are expressed on the Th1 cell surface in association with major histocompatibility molecules. Once the regulatory Th2 cells are specifically activated, they may inhibit inflammatory Th1 cells through a non-specific bystander mechanism. A variety of strategies have been used by us to identify candidate disease-associated TCR V genes present on pathogenic Th1 cells, including BV5S2, BV6S5, and BV13SI in MS, BV3, BV14, and BV17 in RA, and BV3 and BV13S1 in psoriasis. TCR peptides corresponding to the mid region of these BV genes were found to be consistently immunogenic in vivo when administered either i.d. in saline or i.m. in incomplete Freund's adjuvant (IFA). In MS patients, repeated injection of low doses of peptides (100-300 microg) significantly boosted the number of TCR-reactive Th2 cells. These activated cells secreted cytokines, including IL-10, that are known to inhibit inflammatory Th1 cells. Cytokine release could also be induced in TCR-reactive Th2 cells by direct cell-cell contact with Th1 cells expressing the target V gene. These findings indicate the potential of regulatory Th2 cells to inhibit not only the target Th1 cells, but also bystander Th1 cells expressing different V genes specific for other autoantigens. TCR peptide vaccines have been used in our studies to treat a total of 171 MS patients (6 trials), 484 RA patients (7 trials), and 177 psoriasis patients (2 trials). Based on this experience in 824 patients with autoimmune diseases, TCR peptide vaccination is safe and well tolerated, and can produce significant clinical improvement in a subset of patients that respond to immunization. TCR peptide vaccination represents a promising approach that is well-suited for treating complex autoimmune diseases.

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Year:  2001        PMID: 11519731     DOI: 10.1023/a:1010951706830

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  99 in total

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Authors:  D A Norris; J B Travers; D Y Leung
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Journal:  Arthritis Rheum       Date:  1994-10

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Authors:  F Mokhtarian; D E McFarlin; C S Raine
Journal:  Nature       Date:  1984 May 24-30       Impact factor: 49.962

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Review 3.  Autoantigen complementarity: a new theory implicating complementary proteins as initiators of autoimmune disease.

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Review 4.  Diabetes tolerogenic vaccines targeting antigen-specific inflammation.

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5.  Analysis of the interindividual conservation of T cell receptor alpha- and beta-chain variable regions gene in the peripheral blood of patients with systemic lupus erythematosus.

Authors:  W Luo; L Ma; Q Wen; N Wang; M-Q Zhou; X-N Wang
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Review 6.  Vaccines for multiple sclerosis: progress to date.

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Journal:  CNS Drugs       Date:  2008       Impact factor: 5.749

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8.  Age-related CD8 T cell clonal expansions constrict CD8 T cell repertoire and have the potential to impair immune defense.

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9.  LYRA, a webserver for lymphocyte receptor structural modeling.

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10.  Vaccination with single chain antigen receptors for islet-derived peptides presented on I-A(g7) delays diabetes in NOD mice by inducing anergy in self-reactiveT-cells.

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