The Synthetic Triterpenoid, CDDO, Suppresses Alloreactive T Cell Responses and Reduces Murine Early Acute Graft-versus-Host Disease Mortality

• Published in: Biology of blood and marrow transplantation 2007-05, Vol.13 (5), p.521-529
• Main Authors: Sun, Kai, Li, Minghui, Konopleva, Marina, Konoplev, Sergej, Stephens, L. Clifton, Kornblau, Steven M, Frolova, Olga, Wilkins, Danice E.C, Ma, Weihong, Welniak, Lisbeth A, Andreeff, Michael, Murphy, William J
• Format: Article
• Language: English
• Subjects: Allogeneic hematopoietic stem cell transplantation (allo-HSCT); Animals; Anti-Inflammatory Agents - pharmacology; Apoptosis - drug effects; Disease Models, Animal; Female; Graft vs Host Disease - prevention & control; Hematology, Oncology and Palliative Medicine; Hematopoietic Stem Cell Transplantation - adverse effects; Lymphocyte Culture Test, Mixed; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mixed lymphocyte responses; Oleanolic Acid - analogs & derivatives; Oleanolic Acid - pharmacology; T-Lymphocytes - drug effects; Transplantation, Homologous - adverse effects
• ISSN: 1083-8791; 1523-6536
• DOI: 10.1016/j.bbmt.2006.12.453

Abstract Acute graft-versus-host disease (aGVHD) still remains one of the life-threatening complications following allogeneic hematopoietic stem cell transplantation (allo-HSCT). Immunomodulation of alloreactive donor T cell responses, as well as cytokine secretion is a potential therapeutic approach for the prevention of aGVHD. The synthetic triterpenoid, CDDO (2-cyano-3, 12-dioxooleana-1, 9-dien-28-oic acid), exhibits potent antitumor activity and has also been shown to mediate anti-inflammatory and immunomodulatory effects. We therefore wanted to assess the effects of CDDO on early lethal aGVHD. In this study, we found that CDDO significantly inhibited in vitro mixed lymphocyte responses and preferentially promoted the apoptosis of proliferating but not resting alloreactive T cells. Using a full major histocompatibility complex (MHC)-disparate murine aGVHD model, we found that the administration of CDDO immediately after transplantation significantly decreased liver pathology as determined by histologic assessment and prolonged survival in mice. Importantly, administration of CDDO did not adversely impair donor myeloid reconstitution as determined by peripheral blood cell count and the extent of donor chimerism. These findings indicate that CDDO has a significant immunomodulatory effects in vitro and on early lethal aGVHD development, particularly affecting the liver, in a murine allo-HSCT model.