Abstract
The recent interest for Th17 cells immediately raised questions about their possible involvement in allogeneic processes. Indeed, IL-17-producing innate immune cells and Th17 cells have now been related to allograft rejection and ischemia-reperfusion injury in clinical settings and in experimental models. Some of them clearly established a link between the presence of these cells and the development of long-term graft dysfunction. A pivotal role of a Th17-mediated pathway in transplant damage has been demonstrated independently of MHC disparities with T cells recognizing either autoantigen or minor transplantation antigen. The ambiguous relationship between regulatory T cells (Treg) and Th17 cells also complicates Treg-based therapy. Herein, we briefly discuss recent studies reporting Th17 and IL-17 involvements in allograft rejection processes.
L-MC, BV, and PL are first coauthors.
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Acknowledgments
Ph. LM is supported by a grant from the Fonds National de la Recherche Scientifique (FNRS/FRSM) and B.V. by a grant from the SociƩtƩ Francophone de Transplantation (SFT). ALM is a researcher associate from the FNRS. A part of this work was supported by a ROTRF grant (Roche Organ Transplantation Research Foundation)
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Charbonnier, LM., Vokaer, B., LemaƮtre, P., Moine, A.L. (2013). Th17 Cells in Transplantation: Actors or Innocent Bystanders?. In: Quesniaux, V., Ryffel, B., Padova, F. (eds) IL-17, IL-22 and Their Producing Cells: Role in Inflammation and Autoimmunity. Progress in Inflammation Research. Springer, Basel. https://doi.org/10.1007/978-3-0348-0522-3_13
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