Polchert David, Sobinsky Justin, Douglas Gw, Kidd Martha, Moadsiri Ada, Reina Eduardo, Genrich Kristyn, Mehrotra Swati, Setty Suman, Smith Brett, Bartholomew Amelia
Department of Surgery, University of Illinois-Chicago, Chicago, IL 60612, USA.
Eur J Immunol. 2008 Jun;38(6):1745-55. doi: 10.1002/eji.200738129.
Graft versus host disease (GVHD), mediated by donor T cells, is a significant source of morbidity and mortality following allogeneic stem cell transplantation. Mesenchymal stem cells (MSC) can successfully treat ongoing graft versus host disease, presumably due to their ability to suppress donor T cell proliferation. Little is known about the potential of MSC to prevent GVHD. Here we show that bone marrow-isolated MSC can suppress the development of GVHD if given after donor T cell recognition of antigen. IFN-gamma was required to initiate MSC efficacy. Recipients of IFN-gamma(-/-) T cells did not respond to MSC treatment and succumbed to GVHD. MSC, pre-treated with IFN-gamma, became immediately active and could suppress GVHD more efficiently than a fivefold-greater number of MSC that were not activated. When given at the time of bone marrow transplantation, activated MSC could prevent GVHD mortality (100% survival, p=0.006). MSC activation was dependent on the magnitude of IFN-gamma exposure, with increased IFN-gamma exposure leading to increased MSC suppression of GVHD. Activated MSC present a new strategy for preventing GVHD using fewer MSC.
移植物抗宿主病(GVHD)由供体T细胞介导,是异基因干细胞移植后发病和死亡的重要原因。间充质干细胞(MSC)能够成功治疗正在发生的移植物抗宿主病,这可能是由于它们具有抑制供体T细胞增殖的能力。关于MSC预防GVHD的潜力知之甚少。在此我们表明,如果在供体T细胞识别抗原后给予骨髓分离的MSC,其可以抑制GVHD的发展。启动MSC的功效需要γ干扰素(IFN-γ)。IFN-γ(-/-)T细胞的受体对MSC治疗无反应,并死于GVHD。用IFN-γ预处理的MSC立即变得活跃,并且比未激活的多五倍数量的MSC更有效地抑制GVHD。在骨髓移植时给予激活的MSC,可以预防GVHD死亡(100%存活,p = 0.006)。MSC的激活取决于IFN-γ暴露的程度,IFN-γ暴露增加会导致MSC对GVHD的抑制作用增强。激活的MSC为使用更少的MSC预防GVHD提供了一种新策略。