4.2 Article

Interleukin 17 Is Not Required for Autoimmune-Mediated Pathologic Damage during Chronic Graft-versus-Host Disease

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 16, Issue 1, Pages 123-128

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2009.09.008

Keywords

Chronic graft-versus-host disease; Autoimmunity; Interleukin 17

Funding

  1. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL064603, R01HL081650] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK083358] Funding Source: NIH RePORTER
  3. NHLBI NIH HHS [R01 HL064603-08, R01 HL064603, R01 HL081650-02, HL081650, R01 HL081650, HL064603] Funding Source: Medline
  4. NIDDK NIH HHS [R01 DK083358] Funding Source: Medline

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The transition from acute to chronic graft-versus-host disease (aGVHD, cGVHD) is characterized by the progressive loss of self-tolerance and the development of autoimmune manifestations. Interleukin 17 (IL-17) is a proinflammatory cytokine that has been shown to play a prominent role in autoimmune disorders in the nontransplant setting, but the extent to which IL-17 is necessary for the autoimmunity that occurs as a consequence of GVHD is not known. In this study, we demonstrate using a combination of antibody-based and genetic approaches that IL-17 is not required for the loss of self-tolerance and resulting CD4(+) T cell-dependent pathologic damage that occurs during the evolution from aGVHD to cGVHD. Rather, THI cells and other proinflammatory cytokines are fully competent to promote autoimmune-mediated tissue damage. Thus, the selective targeting of IL-17 may not be a viable clinical strategy for preventing the autoimmune manifestations that develop during cGVHD. Biol Blood Marrow Transplant 16: 123-128 (2010) (C) 2010 American Society for Blood and Marrow Transplantation

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