Author
Listed:
- Naresha Saligrama
(Stanford University School of Medicine
Stanford University School of Medicine)
- Fan Zhao
(Stanford University School of Medicine)
- Michael J. Sikora
(Stanford University School of Medicine)
- William S. Serratelli
(Stanford University School of Medicine)
- Ricardo A. Fernandes
(Stanford University School of Medicine)
- David M. Louis
(Stanford University School of Medicine)
- Winnie Yao
(Stanford University School of Medicine)
- Xuhuai Ji
(Stanford University School of Medicine)
- Juliana Idoyaga
(Stanford University School of Medicine)
- Vinit B. Mahajan
(Stanford University
Veterans Affairs Palo Alto Health Care)
- Lars M. Steinmetz
(Stanford University School of Medicine
Stanford University
Genome Biology Unit)
- Yueh-Hsiu Chien
(Stanford University School of Medicine
Stanford University School of Medicine
Stanford University)
- Stephen L. Hauser
(University of California)
- Jorge R. Oksenberg
(University of California)
- K. Christopher Garcia
(Stanford University School of Medicine
Stanford University School of Medicine
Stanford University School of Medicine)
- Mark M. Davis
(Stanford University School of Medicine
Stanford University School of Medicine
Stanford University School of Medicine)
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.
Suggested Citation
Naresha Saligrama & Fan Zhao & Michael J. Sikora & William S. Serratelli & Ricardo A. Fernandes & David M. Louis & Winnie Yao & Xuhuai Ji & Juliana Idoyaga & Vinit B. Mahajan & Lars M. Steinmetz & Yue, 2019.
"Opposing T cell responses in experimental autoimmune encephalomyelitis,"
Nature, Nature, vol. 572(7770), pages 481-487, August.
Handle:
RePEc:nat:nature:v:572:y:2019:i:7770:d:10.1038_s41586-019-1467-x
DOI: 10.1038/s41586-019-1467-x
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