抗原提呈细胞
抗原呈递
CD40
免疫学
抗原
生物
免疫系统
细胞毒性T细胞
T细胞
B细胞
B-1电池
白细胞介素21
幼稚B细胞
细胞生物学
抗体
体外
生物化学
作者
Zhaolin Hua,Baidong Hou
摘要
Abstract B cells have been known for their ability to present antigens to T cells for almost 40 years. However, the precise roles of B cell antigen presentation in various immune responses are not completely understood. The term “professional” antigen‐presenting cells (APCs) was proposed to distinguish APCs that are required for initiating the immune responses from those use antigen presentation to enhance their own effector functions. Unlike dendritic cells, which are defined as professional APCs for their well‐established functions in activating naive T cells, B cells have been shown in the past to mostly present antigens to activated CD4+ T cells mainly to seek help from T helper cells. However, recent evidence suggested that B cells can act as professional APCs under infectious conditions or conditions mimicking viral infections. B cell antigen receptors (BCRs) and the innate receptor Toll‐like receptors are activated synergistically in response to pathogens or virus‐like particles, under which conditions B cells are not only potent but also the predominant APCs to turn naive CD4+ T cells into T follicular helper cells. The discovery of B cells as professional APCs to initiate CD4+ T cell response provides a new insight for both autoimmune diseases and vaccine development.
科研通智能强力驱动
Strongly Powered by AbleSci AI