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大鼠模型中心脏和肾脏同种异体移植耐受的转移。

Transfer of tolerance to heart and kidney allografts in the rat model.

作者信息

Jovanovic Vojislav, Lair David, Soulillou Jean-Paul, Brouard Sophie

机构信息

INSERM U643, Institut de transplantation et de recherche en transplantation, Nantes, France.

出版信息

Transpl Int. 2008 Mar;21(3):199-206. doi: 10.1111/j.1432-2277.2007.00599.x. Epub 2007 Dec 5.

Abstract

Long-term allograft acceptance can be induced in the rat using a variety of maneuvers. One of the cardinal features of some models of tolerance is that once the tolerance state has been established, it can be perpetuated to naive recipients by the adoptive transfer of donor-specific regulatory cells. Such adoptive transfer studies have also addressed the capacity of T-cell subpopulations and non-T cells to transfer tolerance. However, tolerance cannot be transferred in all models. The underlying reasons for this are unclear with some studies pointing towards dose-dependent aspects and timing of expansion of T regulatory cells following tolerance transfer. Further exploration of this phenomenon will help us to understand better the mechanisms upon which allograft tolerance is based, and will provide new perspectives for further experimental studies.

摘要

使用多种方法可在大鼠中诱导长期同种异体移植接受。某些耐受模型的一个主要特征是,一旦建立了耐受状态,通过供体特异性调节细胞的过继转移,它可以延续到未接触过抗原的受体。此类过继转移研究也探讨了T细胞亚群和非T细胞传递耐受的能力。然而,并非所有模型都能传递耐受。其根本原因尚不清楚,一些研究指出这与耐受转移后T调节细胞扩增的剂量依赖性方面和时间有关。对这一现象的进一步探索将有助于我们更好地理解同种异体移植耐受所基于的机制,并为进一步的实验研究提供新的视角。

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