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Opposing T cell responses in experimental autoimmune encephalomyelitis

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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