Trenado Aurélie, Charlotte Frédéric, Fisson Sylvain, Yagello Micael, Klatzmann David, Salomon Benoit L, Cohen José L
Biologie et Thérapeutique des Pathologies Immunitaires, Centre National de la Recherche Scientifique, Université Pierre et Marie Curie, Unité Mixte de Recherche 7087, Hôpital Pitié-Salpêtrière, 83 boulevard de l'Hôpital, F-75651 Paris Cedex 13, France.
J Clin Invest. 2003 Dec;112(11):1688-96. doi: 10.1172/JCI17702.
CD4+CD25+ regulatory T cells (Treg's) play a pivotal role in preventing organ-specific autoimmune diseases and in inducing tolerance to allogeneic organ transplants. We and others recently demonstrated that high numbers of Treg's can also modulate graft-versus-host disease (GVHD) if administered in conjunction with allogeneic hematopoietic stem cell transplantation in mice. In a clinical setting, it would be impossible to obtain enough freshly purified Treg's from a single donor to have a therapeutic effect. Thus, we performed regulatory T cell expansion ex vivo by stimulation with allogeneic APCs, which has the additional effect of producing alloantigen-specific regulatory T cells. Here we show that regulatory T cells specific for recipient-type alloantigens control GVHD while favoring immune reconstitution. Irrelevant regulatory T cells only mediate a partial protection from GVHD. Preferential survival of specific regulatory T cells, but not of irrelevant regulatory T cells, was observed in grafted animals. Additionally, the use of specific regulatory T cells was compatible with some form of graft-versus-tumor activity. These data suggest that recipient-type specific Treg's could be preferentially used in the control of GVHD in future clinical trials.
CD4+CD25+调节性T细胞(Treg细胞)在预防器官特异性自身免疫性疾病以及诱导对同种异体器官移植的耐受性方面发挥着关键作用。我们和其他研究人员最近证明,如果在小鼠同种异体造血干细胞移植的同时给予大量Treg细胞,它们也能够调节移植物抗宿主病(GVHD)。在临床环境中,要从单个供体获得足够数量的新鲜纯化Treg细胞以产生治疗效果是不可能的。因此,我们通过用同种异体抗原呈递细胞(APC)刺激在体外进行调节性T细胞扩增,这还具有产生同种异体抗原特异性调节性T细胞的额外效果。在此我们表明,针对受体型同种异体抗原的调节性T细胞在控制GVHD的同时有利于免疫重建。无关的调节性T细胞仅介导对GVHD的部分保护作用。在移植动物中观察到特异性调节性T细胞而非无关调节性T细胞的优先存活。此外,使用特异性调节性T细胞与某种形式的移植物抗肿瘤活性是相容的。这些数据表明,在未来的临床试验中,受体型特异性Treg细胞可优先用于控制GVHD。