母体微嵌合-自身免疫性疾病的同种异体靶点还是正常生物学?

Anne M. Stevens MD, PhD
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引用次数: 2

摘要

嵌合是两个不同个体的细胞在一个身体内的状态。胎儿细胞在怀孕期间进入母亲体内,在那里它们可能持续数年的低水平,形成胎儿微嵌合状态。与此同时,母体细胞进入胎儿,导致母体微嵌合,这种嵌合可以持续到成年。造血干细胞移植也会产生嵌合状态,并可能导致慢性多器官炎症的并发症,称为移植物抗宿主病(GVHD)。GVHD与一些自身免疫性疾病如硬皮病、狼疮和肌炎之间的相似性表明嵌合可能参与了两者的发病机制。母体和胎儿血液和组织中的微嵌合与自身免疫性疾病有关。然而,许多健康人体内都有母细胞和胎儿细胞。人类和动物研究已经开始阐明对母体和胎儿微嵌合细胞的正常耐受机制,以及这种耐受如何在慢性炎症疾病状态下被破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maternal microchimerism—Allogenic target of autoimmune disease or Normal Biology?

Chimerism is the state of cells from two distinct individuals living within one body. Fetal cells pass into a mother during pregnancy, where they may persist at low levels for years, creating a state of fetal microchimerism. At the same time, maternal cells pass into the fetus, leading to maternal microchimerism that can persist into adulthood. Hematopoietic stem cell transplantation also creates a state of chimerism, and can lead to a complication of chronic multi-organ inflammation called graft-versus-host disease, (GVHD). The similarities between GVHD and some autoimmune diseases like scleroderma, lupus and myositis suggest that chimerism may be involved in the pathogenesis of both. Maternal and fetal microchimerism in the blood and in tissues have been associated with autoimmune diseases. However, many healthy individuals harbor maternal and fetal cells. Human and animal studies have begun to elucidate the mechanisms for normal tolerance to maternal and fetal microchimeric cells, and how this tolerance may be broken in states of chronic inflammatory disease.

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