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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; Idoyaga, Juliana; Mahajan, Vinit B; Steinmetz, Lars M; Chien, Yueh-Hsiu; Hauser, Stephen L; Oksenberg, Jorge R; Garcia, K Christopher; Davis, Mark M.
Afiliación
  • Saligrama N; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Zhao F; Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, USA.
  • Sikora MJ; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Serratelli WS; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Fernandes RA; Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, USA.
  • Louis DM; Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.
  • Yao W; Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, USA.
  • Ji X; Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, USA.
  • Idoyaga J; Human Immune Monitoring Center, Stanford University School of Medicine, Stanford, CA, USA.
  • Mahajan VB; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Steinmetz LM; Byers Eye Institute, Department of Ophthalmology, Stanford University, Palo Alto, CA, USA.
  • Chien YH; Veterans Affairs Palo Alto Health Care, Palo Alto, CA, USA.
  • Hauser SL; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Oksenberg JR; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, USA.
  • Garcia KC; European Molecular Biology Laboratory (EMBL), Genome Biology Unit, Heidelberg, Germany.
  • Davis MM; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Nature ; 572(7770): 481-487, 2019 08.
Article en En | MEDLINE | ID: mdl-31391585
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.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfocitos T / Encefalomielitis Autoinmune Experimental Límite: Adult / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Nature Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfocitos T / Encefalomielitis Autoinmune Experimental Límite: Adult / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Nature Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos