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[硬皮病中的微嵌合体:十年后]

[Microchimerism in scleroderma: ten years later].

作者信息

Lambert N-C

机构信息

Laboratoire immunogénétique de la polyarthrite rhumatoïde, Inserm UMR639, parc scientifique de Luminy, bâtiment TPR2-entrée A, 1(er) étage, 163, avenue de Luminy, 13288 Marseille cedex 9, France.

出版信息

Rev Med Interne. 2010 Jul;31(7):523-9. doi: 10.1016/j.revmed.2009.07.017. Epub 2010 Apr 15.

Abstract

More than ten years ago, the hypothesis that foetal microchimerism (Mc), arising from pregnancy, may have a reaction against the host, or "auto/allo"-immune reaction, has been proposed. More frequent and quantitatively larger foetal Mc found in blood from women with systemic sclerosis (SSc), compared to matched healthy women, argued this hypothesis. Since, Mc has been investigated in SSc and many diseases; however, results were often contradictory. Several explanations are discussed in the current review to understand the controversy and reveal interesting points. Ten years of research allowed to understand that a microchimeric cell is capable of the worst as well as the best depending upon specific factors (environmental, genetics...). Reversion to a non-aggressive phenotype seems possible and gives therapeutic hope.

摘要

十多年前,有人提出了这样一种假说:孕期产生的胎儿微嵌合体(Mc)可能会对宿主产生反应,即“自身/同种异体”免疫反应。与相匹配的健康女性相比,在系统性硬化症(SSc)女性血液中发现的胎儿Mc更频繁且数量更多,这支持了这一假说。此后,人们对SSc和许多疾病中的Mc进行了研究;然而,结果往往相互矛盾。本综述讨论了几种解释,以理解其中的争议并揭示有趣的观点。十年的研究让我们明白,微嵌合细胞根据特定因素(环境、遗传学等)既可能产生最坏的影响,也可能带来最好的结果。恢复为非侵袭性表型似乎是可能的,这带来了治疗希望。

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