氨肽酶
内质网
免疫系统
肽
抗原呈递
主要组织相容性复合体
酶
生物
癌症免疫疗法
免疫疗法
抗原
免疫学
计算生物学
生物化学
T细胞
氨基酸
亮氨酸
作者
Dimitris Georgiadis,Anastasia Mpakali,Despoina Koumantou,Efstratios Stratikos
标识
DOI:10.2174/0929867325666180214111849
摘要
Endoplasmic Reticulum aminopeptidase 1 and 2 are two homologous enzymes that help generate peptide ligands for presentation by Major Histocompatibility Class I molecules. Their enzymatic activity influences the antigenic peptide repertoire and indirectly controls adaptive immune responses. Accumulating evidence suggests that these two enzymes are tractable targets for the regulation of immune responses with possible applications ranging from cancer immunotherapy to treating inflammatory autoimmune diseases. Here, we review the state-of-the-art in the development of inhibitors of ERAP1 and ERAP2 as well as their potential and limitations for clinical applications.
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