Literature DB >> 22226114

The IL-17 differentiation pathway and its role in transplant outcome.

Jonathan S Serody1, Geoffrey R Hill.   

Abstract

The limitations of allogeneic transplantation are graft-versus-host disease (both acute and chronic), infection, and relapse. Acute GVHD has traditionally been thought of as a Th1-mediated disease with inflammatory cytokines (eg, interferon [IFN]-γ and tumor necrosis factor [TNF]) and cellular cytolysis mediating apoptotic target tissue damage in skin, gut, and liver. Chronic GVHD has not fit neatly into either Th1 or Th2 (eg, IL-4, IL-13) paradigms. Increasingly, the Th17 pathway of differentiation has been shown to play important roles in acute and chronic GVHD (aGVHD, cGVHD), particularly in relation to skin and lung disease. Here we discuss the IL-17 pathway of T cell differentiation and the accumulating evidence suggesting it represents an important new target for the control of deleterious alloimmune responses.
Copyright © 2012 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22226114      PMCID: PMC3588169          DOI: 10.1016/j.bbmt.2011.10.001

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  53 in total

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7.  Recombinant human granulocyte colony-stimulating factor significantly decreases the expression of CXCR3 and CCR6 on T cells and preferentially induces T helper cells to a T helper 17 phenotype in peripheral blood harvests.

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5.  Regulation of pulmonary graft-versus-host disease by IL-26+CD26+CD4 T lymphocytes.

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6.  Adoptively transferred donor IL-17-producing CD4+ T cells augment, but IL-17 alleviates, acute graft-versus-host disease.

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9.  Proteomics analysis reveals a Th17-prone cell population in presymptomatic graft-versus-host disease.

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Review 10.  Chronic graft-versus-host disease: biological insights from preclinical and clinical studies.

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