4.5 Review

Lipids hide or step aside for CD1-autoreactive T cell receptors

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CURRENT OPINION IN IMMUNOLOGY
卷 52, 期 -, 页码 93-99

出版社

CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2018.04.013

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资金

  1. National Institutes of Health [R01 AR048632]
  2. National Health and Medical Research Council
  3. Wellcome Trust
  4. Australian Research Council
  5. ARC Laureate Fellowship
  6. Translation Accelerator Grant from the Human Skin Disease Resource Center at Brigham and Women's Hospital
  7. Harvard Medical School [NIH P30 AR069625]
  8. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR048632, P30AR069625] Funding Source: NIH RePORTER

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Peptide and lipid antigens are presented to T cells when bound to MHC or CD1 proteins, respectively. The general paradigm of T cell antigen recognition is that T cell receptors (TCRs) co-recognize an epitope comprised of the antigen and antigen presenting molecule. Here we review the latest studies in which T cells operate outside the co-recognition paradigm: TCRs can broadly contact CD1 itself, but not the carried lipid. The essential structural feature in these new mechanisms is a large 'antigen free' zone on the outer surface of certain antigen presenting molecules. Whereas peptides dominate the exposed surface of MHC-peptide complexes, all human CD1 proteins have a closed, antigen-free surface, which is known as the A' roof. These new structural models help to interpret recent biological studies of CD1 autoreactive T cells in vivo, which have now been broadly observed in studies on TCR-transgenic mice, healthy humans and patients with autoimmune disease.

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