UCLA Immunogenetics Center, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, United States.
Curr Opin Immunol. 2009 Oct;21(5):557-62. doi: 10.1016/j.coi.2009.08.002. Epub 2009 Sep 11.
Transplant recipients exhibiting posttransplant antibodies are at a higher risk for acute and chronic antibody mediated rejection (AMR). The primary alloantigens recognized by antibodies in recipients with AMR are the highly polymorphic HLA class I and class II molecules expressed on the surface of the endothelial cells (ECs) of the graft. Traditionally, anti-HLA antibodies were thought to mediate graft injury through complement-dependent mechanisms. However, recent studies indicate that antibodies can also contribute to alterations in EC function through complement-independent mechanisms by transducing intracellular signals. Anti-HLA antibodies transduce signals that are both pro-inflammatory and pro-proliferative suggesting mechanistic roles in acute and chronic AMR.
移植受者出现移植后抗体后,发生急性和慢性抗体介导排斥反应(AMR)的风险更高。AMR 受者抗体识别的主要同种抗原是表达在移植物内皮细胞(EC)表面的高度多态性 HLA Ⅰ类和Ⅱ类分子。传统上,认为抗 HLA 抗体通过补体依赖性机制介导移植物损伤。然而,最近的研究表明,抗体也可以通过转导细胞内信号通过补体非依赖性机制导致 EC 功能改变。抗 HLA 抗体转导的信号既有促炎作用又有促增殖作用,提示在急性和慢性 AMR 中具有机制作用。