Patel Jignesh K, Kobashigawa Jon A
Cedars-Sinai Heart Institute, 8700 Beverly Boulevard, Los Angeles, CA 90048, USA.
Future Cardiol. 2012 Jul;8(4):623-35. doi: 10.2217/fca.12.27.
The diagnosis of antibody-mediated rejection (AMR) has presented a challenge due to the pleiomorphic immunologic responses that represent the condition. A consensus with regard to its pathological diagnosis continues to evolve. Due to an increasing number of sensitized patients undergoing heart transplantation, its incidence appears to be on the rise and the condition is associated with worse outcomes than acute cellular rejection. Treatment of AMR is also more difficult and response to increases in conventional immunosuppression is often limited. Risk factors for AMR include the use of ventricular assist devices, prior exposure to blood products, allografts and multiparity. Detection of alloantibodies with a high specificity and sensitivity allows risk stratification of recipients at potential risk of AMR. Desensitization and AMR treatment strategies are focused on several therapeutic targets, including suppression of T and B cells and elimination or inhibition of circulating antibodies.
由于抗体介导的排斥反应(AMR)所呈现的多形性免疫反应,其诊断一直是一项挑战。关于其病理诊断的共识仍在不断发展。由于接受心脏移植的致敏患者数量不断增加,其发病率似乎在上升,且该病症与比急性细胞排斥更差的预后相关。AMR的治疗也更加困难,对传统免疫抑制增加的反应往往有限。AMR的危险因素包括使用心室辅助装置、既往接触血液制品、同种异体移植物和多胎妊娠。检测具有高特异性和敏感性的同种抗体可对有AMR潜在风险的受者进行风险分层。脱敏和AMR治疗策略集中于几个治疗靶点,包括抑制T细胞和B细胞以及消除或抑制循环抗体。