Department of Diabetes Complications & Metabolism, Arthur Riggs Diabetes & Metabolism Research Institute, City of Hope National Medical Center, Duarte, California, USA.
Department of Molecular & Cellular Endocrinology, Arthur Riggs Diabetes & Metabolism Research Institute, City of Hope National Medical Center, Duarte, California, USA.
Clin Transl Med. 2024 Feb;14(2):e1584. doi: 10.1002/ctm2.1584.
Cluster of differentiation 47 (CD47) occupies the outer membrane of human cells, where it binds to soluble and cell surface receptors on the same and other cells, sculpting their topography and resulting in a pleiotropic receptor-multiligand interaction network. It is a focus of drug development to temper and accentuate CD47-driven immune cell liaisons, although consideration of on-target CD47 effects remain neglected. And yet, a late clinical trial of a CD47-blocking antibody was discontinued, existent trials were restrained, and development of CD47-targeting agents halted by some pharmaceutical companies. At this point, if CD47 can be exploited for clinical advantage remains to be determined. Herein an airing is made of the seemingly conflicting actions of CD47 that reflect its position as a junction connecting receptors and signalling pathways that impact numerous human cell types. Prospects of CD47 boosting and blocking are considered along with potential therapeutic implications for autoimmune diseases and cancer.
分化群 47(CD47)占据人体细胞的外膜,在那里它与同一细胞和其他细胞表面的可溶性和细胞表面受体结合,塑造它们的拓扑结构,并导致多效性受体-多配体相互作用网络。调节和强调 CD47 驱动的免疫细胞联系是药物开发的重点,尽管对靶标 CD47 效应的考虑仍然被忽视。然而,一种 CD47 阻断抗体的后期临床试验被停止,现有的试验受到限制,一些制药公司停止了 CD47 靶向药物的开发。在这一点上,如果 CD47 可以被利用为临床优势还有待确定。本文阐述了 CD47 看似矛盾的作用,反映了它作为连接受体和信号通路的连接点的位置,这些受体和信号通路影响着众多人类细胞类型。同时还考虑了 CD47 增强和阻断的前景,以及它们在自身免疫性疾病和癌症中的潜在治疗意义。