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Regulation of self-tolerance by CD80/CD86 interactions
Authors:Pin Lu  Yue Lynn Wang  Peter S Linsley
Affiliation:aDepartment of Immunomodulation, Bristol-Myers Squibb Pharmaceutical Research Institute, 3005 First Avenue, Seattle, WA 98121, USA;bDivision of Molecular Diagnostics, Department of Pathology, University of Pittsburgh, 3550 Terrace Street, S770A Scaife Hall, Pittsburgh, PA 15261, USA
Abstract:Antigen presentation by CD80/CD86-positive ‘professional APCs’ induces T-cell activation, whereas antigen presentation in the absence of sufficient CD80/CD86 costimulation may induce a form of tolerance. Blocking CD80/CD86 costimulation inhibits autoimmune disease progression in a variety of animal models, but whether these effects result from restoration of self-tolerance or temporary disease blockade is still unclear. The individual roles of CD80 and CD86 in autoimmune diseases are complicated by multiple factors in vivo. Data from B7 gene knockout mice further clarify the importance of CD80/CD86 in the regulation of T-cell activation and tolerance.
Keywords:Abbreviations: APC antigen-presenting cell   CTLA-4 cytotoxic T lymphocyte antigen-4   EAE experimental allergic encephalomyelitis   IL interleukin   IFN interferon   NOD non-obese diabetes
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