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10.3390/ijms19030819

http://scihub22266oqcxt.onion/10.3390/ijms19030819
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C5877680!5877680!29534522
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suck abstract from ncbi


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pmid29534522      Int+J+Mol+Sci 2018 ; 19 (3): ä
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  • Regulation of T-Cell Signaling by Post-Translational Modifications in Autoimmune Disease #MMPMID29534522
  • Kuwabara T; Matsui Y; Ishikawa F; Kondo M
  • Int J Mol Sci 2018[Mar]; 19 (3): ä PMID29534522show ga
  • The adaptive immune system involves antigen-specific host defense mechanisms mediated by T and B cells. In particular, CD4+ T cells play a central role in the elimination of pathogens. Immunological tolerance in the thymus regulates T lymphocytes to avoid self-components, including induction of cell death in immature T cells expressing the self-reactive T-cell receptor repertoire. In the periphery, mature T cells are also regulated by tolerance, e.g., via induction of anergy or regulatory T cells. Thus, T cells strictly control intrinsic signal transduction to prevent excessive responses or self-reactions. If the inhibitory effects of T cells on these mechanisms are disrupted, T cells may incorrectly attack self-components, which can lead to autoimmune disease. The functions of T cells are supported by post-translational modifications, particularly phosphorylation, of signaling molecules, the proper regulation of which is controlled by endogenous mechanisms within the T cells themselves. In recent years, molecular targeted agents against kinases have been developed for treatment of autoimmune diseases. In this review, we discuss T-cell signal transduction in autoimmune disease and provide an overview of acetylation-mediated regulation of T-cell signaling pathways.
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