Publikation: On the role of the immunoproteasome in transplant rejection
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The immunoproteasome is expressed in cells of hematopoietic origin and is induced during inflammation by IFN-γ. Targeting the immunoproteasome with selective inhibitors has been shown to be therapeutically effective in pre-clinical models for autoimmune diseases, colitis-associated cancer formation, and transplantation. Immunoproteasome inhibition prevents activation and proliferation of lymphocytes, lowers MHC class I cell surface expression, reduces the expression of cytokines of activated immune cells, and curtails T helper 1 and 17 cell differentiation. This might explain the in vivo efficacy of immunoproteasome inhibition in different pre-clinical disease models for autoimmunity, cancer, and transplantation. In this review, we summarize the effect of immunoproteasome inhibition in different animal models for transplantation.
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BASLER, Michael, Jun LI, Marcus GRÖTTRUP, 2019. On the role of the immunoproteasome in transplant rejection. In: Immunogenetics. 2019, 71(3), pp. 263-271. ISSN 0093-7711. eISSN 1432-1211. Available under: doi: 10.1007/s00251-018-1084-0BibTex
@article{Basler2019-03immun-43313, year={2019}, doi={10.1007/s00251-018-1084-0}, title={On the role of the immunoproteasome in transplant rejection}, number={3}, volume={71}, issn={0093-7711}, journal={Immunogenetics}, pages={263--271}, author={Basler, Michael and Li, Jun and Gröttrup, Marcus} }
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