Opposing T cell responses in experimental autoimmune encephalomyelitis.

Saligrama, Naresha; Zhao, Fan; Sikora, Michael J; Serratelli, William S; Fernandes, Ricardo A; Louis, David M; Yao, Winnie; Ji, Xuhuai et al. · Nature · 2019

basic_science · Level V

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Abstract

Experimental autoimmune encephalomyelitis is a model for multiple sclerosis. Here we show that induction generates successive waves of clonally expanded CD4<sup>+</sup>, CD8<sup>+</sup> and γδ<sup>+</sup> T cells in the blood and central nervous system, similar to gluten-challenge studies of patients with coeliac disease. We also find major expansions of CD8<sup>+</sup> T cells in patients with multiple sclerosis. In autoimmune encephalomyelitis, we find that most expanded CD4<sup>+</sup> T cells are specific for the inducing myelin peptide MOG<sub>35-55</sub>. By contrast, surrogate peptides derived from a yeast peptide major histocompatibility complex library of some of the clonally expanded CD8<sup>+</sup> T cells inhibit disease by suppressing the proliferation of MOG-specific CD4<sup>+</sup> T cells. These results suggest that the induction of autoreactive CD4<sup>+</sup> T cells triggers an opposing mobilization of regulatory CD8<sup>+</sup> T cells.

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