4.8 Review

Pathogenic CD8T cells in multiple sclerosis and its experimental models

Journal

FRONTIERS IN IMMUNOLOGY
Volume 3, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2012.00064

Keywords

multiple sclerosis; experimental autoimmune encephalomyelitis; T cells; tolerance; autoimmunity; central nervous system; MHC; TCR

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Funding

  1. NIH [RAI088495A, T32 AI 007349]
  2. UMass DERC [DK32520]
  3. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK095077] Funding Source: NIH RePORTER

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A growing body of evidence suggests that autoreactive CD8 T cells contribute to the disease process in multiple sclerosis (MS). Lymphocytes in MS plagues are biased toward the CD8 lineage, and MS patients harbor CD8T cells specific for multiple central nervous system (CNS) antigens. Currently, there are relatively few experimental model systems available to study these pathogenic CD8T cells in vivo. However, the few studies that have been done characterizing the mechanisms used by CD8T cells to induce CNS autoimmunity indicate that several of the paradigms of how CD4 T cells mediate CNS autoimmunity do not hold true for CD8T cells or for patients with MS.Thus, myelin-specific CD4T cells are likely to be one of several important mechanisms that drive CNS disease in MS patients. The focus of this review is to highlight the current models of pathogenic CNS-reactive CD8 T cells and the molecular mechanisms these lymphocytes use when causing CNS inflammation and damage. Understanding how CNS-reactive CD8T cells escape tolerance induction and induce CNS autoimmunity is critical to our ability to propose and test new therapies for MS.

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