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Original Article

Ana C. Anderson^a, Lindsay B. Nicholson^a, Kevin L. Legge^b, Vadim Turchin^a, Habib Zaghouani^b, and Vijay K. Kuchroo^a

^a Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115
^b Department of Microbiology, University of Tennessee, Knoxville, Tennessee 37996
Harvard Institutes of Medicine, Rm. 706, 77 Ave. Louis Pasteur, Boston, MA 02115.617-525-5333617-525-5350

kuchroo{at}cnd.bwh.harvard.edu

The autoreactive T cells that escape central tolerance and form the peripheral self-reactive repertoire determine both susceptibility to autoimmune disease and the epitope dominance of a specific autoantigen. SJL (H-2^s) mice are highly susceptible to the induction of experimental autoimmune encephalomyelitis (EAE) with myelin proteolipid protein (PLP). The two major encephalitogenic epitopes of PLP (PLP 139–151 and PLP 178–191) bind to IA^s with similar affinity; however, the immune response to the PLP 139–151 epitope is always dominant. The immunodominance of the PLP 139–151 epitope in SJL mice appears to be due to the presence of expanded numbers of T cells (frequency of 1/20,000 CD4⁺ cells) reactive to PLP 139–151 in the peripheral repertoire of naive mice. Neither the PLP autoantigen nor infectious environmental agents appear to be responsible for this expanded repertoire, as endogenous PLP 139–151 reactivity is found in both PLP-deficient and germ-free mice. The high frequency of PLP 139–151-reactive T cells in SJL mice is partly due to lack of thymic deletion to PLP 139–151, as the DM20 isoform of PLP (which lacks residues 116–150) is more abundantly expressed in the thymus than full-length PLP. Reexpression of PLP 139–151 in the embryonic thymus results in a significant reduction of PLP 139–151-reactive precursors in naive mice. Thus, escape from central tolerance, combined with peripheral expansion by cross-reactive antigen(s), appears to be responsible for the high frequency of PLP 139–151-reactive T cells.

Key Words: autoimmunity • EAE • T cell receptor repertoire • thymic selection • major histocompatibility complex and disease

© 2000 The Rockefeller University Press

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