异种药物、嵌合和器官移植后耐受的诱导。

Therapeutic immunology Pub Date : 1994-06-01
C P Delaney, A W Thomson, A J Demetris, T E Starzl
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引用次数: 0

摘要

器官移植后的成功结果在很大程度上归功于现代免疫抑制剂的效力和特异性。尽管在临床实践中尚未常规实现对移植物异体抗原的无药物无反应性,但最近对细胞嵌合的重要性的认识已经引入了一个概念,可以解释移植物耐受的机制。细胞嵌合是在实体器官移植物中含有的白细胞从供体迁移到宿主后发生的。最近的证据表明,免疫抑制药物可能具有诱导移植物耐受的共同潜力,尽管它们通过不同的机制起作用,并且这种潜力可能通过对供体来源的白细胞的迁移和存活的允许作用来介导。本文简要介绍了免疫抑制药物的作用机制,并分析了这些药物可能用于诱导与移植物耐受相关的嵌合的不同方法。此外,我们描述了正在进行的临床研究,在这些研究中,实体器官移植后产生的嵌合物与供体骨髓相增强,试图促进耐受性的诱导。
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Xenobiotics, chimerism and the induction of tolerance following organ transplantation.

The successful results seen after organ transplantation are largely attributable to the potency and specificity of modern immunosuppressive agents. Although drug-free unresponsiveness to graft alloantigens has not been routinely achieved in clinical practice, recent appreciation of the importance of cell chimerism, which develops after the migration from donor to host of leukocytes contained in solid organ grafts, has introduced a concept which may explain the mechanism of graft tolerance. Recent evidence has indicated that immunosuppressive drugs may have a common potential to induce graft tolerance, even though they act through diverse mechanisms, and that this potential may be mediated by a permissive effect on the migration and survival of donor-derived leukocytes. This review briefly examines the mechanisms by which immunosuppressive drugs function and analyses the different methods which these agents might use to induce chimerism associated with graft tolerance. Furthermore, we describe ongoing clinical studies in which the chimerism produced after solid organ transplantation is augmented with donor bone marrow in an attempt to facilitate the induction of tolerance.

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