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树突状细胞、耐受性与器官移植排斥反应的治疗

Dendritic cells,tolerance and therapy of organ allograft rejection.

作者信息

Raimondi Giorgio, Thomson Angus W

机构信息

Thomas E. Starzl Transplantation Institute and Department of Surgery and Immunology, University of Pittsburgh, Pittsburgh, Pa., USA.

出版信息

Contrib Nephrol. 2005;146:105-120. doi: 10.1159/000082071.

DOI:10.1159/000082071
PMID:15567925
Abstract

Donor dendritic cells (DCs) and those of host origin play key roles in the instigation and maintenance of immune responses to organ allografts. In the normal steady state, however, DCs are important for the maintenance of central and peripheral tolerance. Moreover, the presence of those cells in donor hematopoietic cell infusions may facilitate the induction of transplant tolerance. Accrual of information regarding DC tolerogenicity has driven the assessment of DC-based therapy of allograft rejection. Pioneering work demonstrating increased allograft survival after pretransplant infusion of immature donor-derived DC has prompted the evaluation of several approaches to the generation of DCs with tolerogenic/regulatory properties. These include: identification of specific culture conditions for propagation of homogenous populations of immature DCs; pharmacological manipulation of DCs to stabilize their immature/tolerogenic phenotype; and genetic modification of DCs to impair their stimulating ability/enhance their tolerogenicity. These approaches have rendered DCs capable of markedly prolonging experimental allograft (including kidney transplant) survival and promoting donor-specific tolerance. Recently identified molecular signaling pathways that play key roles in the outcome of DC-T cell interaction are likely to become novel targets for manipulation of allograft immunity and for the promotion of transplant tolerance.

摘要

供体树突状细胞(DCs)和宿主来源的树突状细胞在器官同种异体移植免疫反应的激发和维持中起关键作用。然而,在正常稳态下,DCs对于维持中枢和外周耐受很重要。此外,供体造血细胞输注中这些细胞的存在可能有助于诱导移植耐受。关于DCs致耐受性的信息积累推动了基于DCs的同种异体移植排斥治疗的评估。开创性工作表明,移植前输注未成熟的供体来源DC后同种异体移植存活率提高,这促使人们评估了几种产生具有致耐受性/调节特性DCs的方法。这些方法包括:确定用于未成熟DCs同质群体增殖的特定培养条件;对DCs进行药理学操作以稳定其未成熟/致耐受性表型;以及对DCs进行基因改造以削弱其刺激能力/增强其致耐受性。这些方法已使DCs能够显著延长实验性同种异体移植(包括肾移植)的存活时间并促进供体特异性耐受。最近发现的在DC-T细胞相互作用结果中起关键作用的分子信号通路可能会成为操纵同种异体移植免疫和促进移植耐受的新靶点。

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