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Research Article Free access | 10.1172/JCI114610

Clinical modeling of T cell vaccination against autoimmune diseases in rats. Selection of antigen-specific T cells using a mitogen.

F Mor, A W Lohse, N Karin, and I R Cohen

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Isreal.

Find articles by Mor, F. in: PubMed | Google Scholar

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Isreal.

Find articles by Lohse, A. in: PubMed | Google Scholar

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Isreal.

Find articles by Karin, N. in: PubMed | Google Scholar

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Isreal.

Find articles by Cohen, I. in: PubMed | Google Scholar

Published May 1, 1990 - More info

Published in Volume 85, Issue 5 on May 1, 1990
J Clin Invest. 1990;85(5):1594–1598. https://doi.org/10.1172/JCI114610.
© 1990 The American Society for Clinical Investigation
Published May 1, 1990 - Version history
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Abstract

Effective T cell vaccination against experimental autoimmune diseases involves treatment with activated, autoimmune T lymphocytes. The present study was undertaken to learn whether antigen-specific T cells present in low frequency could be selected in vitro without using the specific antigen. The rat models of adjuvant arthritis and experimental autoimmune encephalomyelitis were investigated using proliferation assays and limiting dilution techniques to quantify the changes in reactivity of a heterogenous population of lymphocytes to the relevant antigen. Stimulation with concanavalin A for 2 d and then culture in IL-2-containing medium led to a substantial increase in the activity and frequency of the specific autoimmune T cells. Enrichment of antigen-specific T cells could be demonstrated using lymph node, spleen, or peripheral blood lymphocytes, from rats late in the course of disease. The effect was not evident in lymphocytes from the thymus. These results are relevant to the clinical application of T cell vaccination and to investigation of self-antigens in autoimmune disease.

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