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造血嵌合体诱导耐受的机制:免疫观点。

Mechanisms of Tolerance Induction by Hematopoietic Chimerism: The Immune Perspective.

机构信息

Institute for Cellular Therapeutics and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.

Frankel Laboratory of Experimental Bone Marrow Transplantation, Petach Tikva, Israel.

出版信息

Stem Cells Transl Med. 2017 Mar;6(3):700-712. doi: 10.1002/sctm.16-0358. Epub 2017 Jan 3.

Abstract

Hematopoietic chimerism is one of the effective approaches to induce tolerance to donor-derived tissue and organ grafts without administration of life-long immunosuppressive therapy. Although experimental efforts to develop such regimens have been ongoing for decades, substantial cumulative toxicity of combined hematopoietic and tissue transplants precludes wide clinical implementation. Tolerance is an active immunological process that includes both peripheral and central mechanisms of mutual education of coresident donor and host immune systems. The major stages include sequential suppression of early alloreactivity, establishment of hematopoietic chimerism and suppressor cells that sustain the state of tolerance, with significant mechanistic and temporal overlap along the tolerization process. Efforts to devise less toxic transplant strategies by reduction of preparatory conditioning focus on modulation rather than deletion of residual host immunity and early reinstitution of regulatory subsets at the central and peripheral levels. Stem Cells Translational Medicine 2017;6:700-712.

摘要

造血嵌合是诱导对供体组织和器官移植物的免疫耐受而无需长期免疫抑制治疗的有效方法之一。尽管数十年来一直在努力开发此类方案,但联合造血和组织移植的大量累积毒性排除了广泛的临床实施。耐受是一种主动的免疫过程,包括共存的供体和宿主免疫系统的外周和中枢机制的相互教育。主要阶段包括早期同种异体反应的顺序抑制、造血嵌合和维持耐受状态的抑制细胞的建立,在耐受过程中具有显著的机制和时间重叠。通过减少预备条件来设计毒性较小的移植策略的努力集中在调节而不是删除残留的宿主免疫,并在中枢和外周水平早期重新建立调节亚群。干细胞转化医学 2017;6:700-712.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6668/5442770/be938c306eb0/SCT3-6-0700-g001.jpg

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