A. Shanmugam et al., IN-VIVO CLONAL EXPANSION OF T-LYMPHOCYTES SPECIFIC FOR AN IMMUNODOMINANT N-TERMINAL MYELIN BASIC-PROTEIN EPITOPE IN HEALTHY-INDIVIDUALS, Journal of neuroimmunology, 59(1-2), 1995, pp. 165-172
The role of myelin basic protein (MBP) T cell recognition in the induc
tion of experimental allergic encephalomyelitis (EAE) has been well es
tablished in mice and rats. A remarkable restriction has been observed
in T cell receptor (TCR) genes utilized by encephalitogenic T cell li
nes (TCLs) specific for immunodominant epitopes in these species. Path
ological similarities between this animal model and multiple sclerosis
(MS) has led to consider MBP as a major candidate autoantigen in this
human disorder. Unlike in inbred strains of animals, the T cell respo
nse to MBP in humans is quite heterogenous with regard to fine epitope
specificity. The existence of V alpha and/or V beta restriction in MB
P-specific T cells, from MS patients and healthy controls, is still a
matter of debate. In this study we generated 77 MBP-specific TCLs from
nine healthy donors and showed that peptide 7-27 is one of the most f
requently recognized epitopes. 37% of all epitope-specific TCLs recogn
ized this peptide and p7-27-specific TCLs were generated from seven ou
t of the nine subjects studied. A high level of in vivo clonal expansi
on was observed in p7-27-specific TCLs in several subjects, which howe
ver is not specific of this epitope since this phenomenon was also obs
erved in p85-104- and 149-162-specific TCLs.