학술논문

Opposing T cell responses in experimental autoimmune encephalomyelitis.
Document Type
article
Source
Nature. 572(7770)
Subject
T-Lymphocytes
CD4-Positive T-Lymphocytes
CD8-Positive T-Lymphocytes
Clone Cells
Animals
Mice
Inbred C57BL
Humans
Mice
Celiac Disease
Encephalomyelitis
Autoimmune
Experimental
Myelin-Associated Glycoprotein
Receptors
Antigen
T-Cell
H-2 Antigens
Immunization
Lymphocyte Activation
Adult
Middle Aged
Female
Male
T-Lymphocytes
Regulatory
Young Adult
Inbred C57BL
Encephalomyelitis
Autoimmune
Experimental
Receptors
Antigen
T-Cell
Regulatory
General Science & Technology
Language
Abstract
Experimental autoimmune encephalomyelitis is a model for multiple sclerosis. Here we show that induction generates successive waves of clonally expanded CD4+, CD8+ and γδ+ 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+ T cells in patients with multiple sclerosis. In autoimmune encephalomyelitis, we find that most expanded CD4+ T cells are specific for the inducing myelin peptide MOG35-55. By contrast, surrogate peptides derived from a yeast peptide major histocompatibility complex library of some of the clonally expanded CD8+ T cells inhibit disease by suppressing the proliferation of MOG-specific CD4+ T cells. These results suggest that the induction of autoreactive CD4+ T cells triggers an opposing mobilization of regulatory CD8+ T cells.