Pinelli David F, Ford Mandy L
Emory Transplant Center, Emory University, Woodruff Memorial Research Building, 101 Woodruff Circle, Suite 5105, Atlanta, GA 30322, USA.
Immunotherapy. 2015;7(4):399-410. doi: 10.2217/imt.15.1.
Since the discovery of the CD40-CD154 costimulatory pathway and its critical role in the adaptive immune response, there has been considerable interest in therapeutically targeting this interaction with monoclonal antibodies in transplantation. Unfortunately, initial promise in animal models gave way to disappointment in clinical trials following a number of thromboembolic complications. However, recent mechanistic studies have identified the mechanism of these adverse events, as well as detailed a myriad of interactions between CD40 and CD154 on a wide variety of immune cell types and the critical role of this pathway in generating both humoral and cell-mediated alloreactive responses. This has led to resurgence in interest and the potential resurrection of anti-CD154 and anti-CD40 antibodies as clinically viable therapeutic options.
自从发现CD40 - CD154共刺激通路及其在适应性免疫反应中的关键作用以来,人们对在移植中用单克隆抗体治疗性靶向这种相互作用产生了浓厚兴趣。不幸的是,动物模型中的初步前景在随后出现的一些血栓栓塞并发症的临床试验中化为失望。然而,最近的机制研究已经确定了这些不良事件的机制,并且详细阐述了CD40和CD154在多种免疫细胞类型上的无数相互作用,以及该通路在产生体液和细胞介导的同种异体反应中的关键作用。这导致了人们兴趣的复苏以及抗CD154和抗CD40抗体作为临床上可行的治疗选择的潜在复兴。