The Scripps Research Institute, Department of Immunology and Microbiology, La Jolla, CA 92037, USA.
The Scripps Research Institute, Department of Immunology and Microbiology, La Jolla, CA 92037, USA. Electronic address: https://twitter.com/mmw_lmw.
Trends Immunol. 2019 Apr;40(4):345-357. doi: 10.1016/j.it.2019.01.012. Epub 2019 Mar 4.
Helper T cell induced plasma cells (PCs) that secrete class-switched neutralizing antibody are paramount to effective immunity. Following class-switch recombination (CSR), antigen-activated B cells differentiate into extrafollicular PCs or mature in germinal centers (GCs) to produce high-affinity memory B cells and follicular PCs. Many studies focus on the core transcriptional programs that drive central PC functions of longevity and antibody secretion. However, it is becoming clear that these central programs are further subdivided across antibody isotype with separable transcriptional trajectories. Divergent functions emerge at CSR, persist through PC terminal differentiation and further assort memory PC function following antigen recall. Here, we emphasize recent work that assorts divergent isotype-specific PC function across four major modules of immune protection.
辅助性 T 细胞诱导分泌类别转换中和抗体的浆细胞(PCs)对于有效的免疫至关重要。在类别转换重组(CSR)之后,抗原激活的 B 细胞分化为滤泡外浆细胞或在生发中心(GCs)中成熟,以产生高亲和力的记忆 B 细胞和滤泡浆细胞。许多研究都集中在驱动中央 PC 寿命和抗体分泌的核心转录程序上。然而,现在越来越清楚的是,这些核心程序在抗体同种型之间进一步细分,具有可分离的转录轨迹。在 CSR 时出现不同的功能,在 PC 终末分化过程中持续存在,并在抗原再次刺激时进一步对记忆 PC 功能进行分类。在这里,我们强调了最近的工作,这些工作将不同的同种型特异性 PC 功能分类到四个主要的免疫保护模块中。