| |
|
|
|
|
|
|
|||
|
Blood, 5 March 2009, Vol. 113, No. 10, pp. 2352-2362. Prepublished online as a Blood First Edition Paper on December 4, 2008; DOI 10.1182/blood-2008-08-175448.
Submitted August 21, 2008
Bone Marrow Transplant Program, Medical College of Wisconsin, Milwaukee, WI, United States * Corresponding author; email: wdrobysk{at}mcw.edu.
Damage to the gastrointestinal tract during graft versus host disease (GVHD) from the conditioning regimen in conjunction with alloreactive donor T cells plays a pivotal role in the pathogenesis of this disease. In this study, we have identified secretion of interleukin 23 (IL-23) by donor antigen-presenting cells (APCs) as a critical event in the induction of GVHD of the colon linking conditioning regimen-induced mucosal injury and lipopolysaccharide (LPS) translocation to subsequent proinflammatory cytokine production and GVHD-associated pathological damage. In the absence of donor APC-derived IL-23 secretion, there is a selective and profound reduction in pathological damage as well as a marked reduction in LPS and proinflammatory cytokine production in the colon microenvironment. The downstream proinflammatory effects of IL-23 are dependent upon donor-derived secretion of IFN-
This article has been cited by other articles:
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Copyright © 2008 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||