Scandiuzzi Lisa, Ghosh Kaya, Zang Xingxing
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Discov Med. 2011 Aug;12(63):119-28.
T cell costimulatory and coinhibitory pathways are essential orchestrators and regulators of the adaptive immune response. In recent years, the costimulatory CD28 receptor and B7 ligand families have been expanded to include a total of four and seven members, respectively. Several polymorphisms, mutations, and deletions in both regulatory and protein-coding regions of these genes have subsequently been discovered and evaluated for genetic linkage to various human diseases. Here, we review this evidence as we discuss T cell costimulation and coinhibition in the context of genetic susceptibility to autoimmunity, cancer, and other diseases. As we gain further insight into the functional significance and mechanism of these immunoregulatory pathways by both genetic and immunological approaches, these receptors and ligands are poised to become key targets for immunotherapy.
T细胞共刺激和共抑制途径是适应性免疫反应的重要协调者和调节者。近年来,共刺激CD28受体家族和B7配体家族分别扩展到总共四个和七个成员。随后,在这些基因的调控区和蛋白质编码区发现了几种多态性、突变和缺失,并对其与各种人类疾病的遗传连锁进行了评估。在此,我们在讨论自身免疫性疾病、癌症和其他疾病的遗传易感性背景下的T细胞共刺激和共抑制时,回顾这一证据。随着我们通过遗传学和免疫学方法进一步深入了解这些免疫调节途径的功能意义和机制,这些受体和配体有望成为免疫治疗的关键靶点。