Literature DB >> 24215417

Optimizing the use of regulatory T cells in allotransplantation: recent advances and future perspectives.

Caitlin E Baum1, Beata Mierzejewska, Paul M Schroder, Mithun Khattar, Stanislaw Stepkowski.   

Abstract

Apart from clonal deletion of self-reactive T cells in the thymus, Tregs are the major regulators of immune responses in the periphery and maintain a state of self-tolerance free from autoimmune diseases. Due to their inherent suppressive function, Tregs are being explored for their therapeutic potential in preventing autoimmunity and improving survival of allografts. This review provides recent updates on Treg biology and their use in animal as well as clinical models of transplantation. We discuss potential problems that limit the widespread clinical application of Tregs and provide future perspectives on how to optimize their medical use. Special consideration is given to methods by which Tregs should be isolated and expanded in order to facilitate clinical therapies. We also focus on recent discussions of Treg stability and plasticity, with specific insights into preventing the loss of Treg suppression by allotransplant-mediated inflammation.

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Year:  2013        PMID: 24215417     DOI: 10.1586/1744666X.2013.849573

Source DB:  PubMed          Journal:  Expert Rev Clin Immunol        ISSN: 1744-666X            Impact factor:   4.473


  1 in total

1.  HDAC6-specific inhibitor suppresses Th17 cell function via the HIF-1α pathway in acute lung allograft rejection in mice.

Authors:  Wenyong Zhou; Jun Yang; Gaowa Saren; Heng Zhao; Kejian Cao; Shijie Fu; Xufeng Pan; Huijun Zhang; An Wang; Xiaofeng Chen
Journal:  Theranostics       Date:  2020-05-21       Impact factor: 11.556

  1 in total

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