Human Immunology Team, Center for Infectious Disease Education and Research (CIDER), Osaka University, Suita, Japan.
Laboratory of Experimental Immunology, WPI Immunology Frontier Research Center (IFReC), Osaka University, Suita, Japan.
Curr Protoc. 2021 Nov;1(11):e283. doi: 10.1002/cpz1.283.
Regulatory T cells (Tregs) expressing the transcription factor Foxp3 have a critical role for the control of immune homeostasis. The Treg subgroup T follicular regulatory cells (Tfr) have a specialized function to travel to the B cell follicle and control antibody responses. While Tfr may be identified by their protein or gene expression profiles, the use of in vitro functional assays to determine their suppressive capacity is important to further characterize these cells. Here we present methods for the identification and purification of Tfr from both mice and humans followed by co-culture with B cells and T follicular helper cells (Tfh). The suppressive activity of the Tfr is then assessed by the ability to prevent Tfh-dependent B cell class switching and plasma blast formation measured by flow cytometry and immunoglobulin production in culture supernatants measured by enzyme-linked immunosorbent assay. These assays will also provide in-depth characterization of the functional suppressive capacity of any isolated Tfr or Treg population. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Isolation of murine T follicular regulatory cells Basic Protocol 2: Measurement of murine T follicular regulatory cell suppressive function Basic Protocol 3: Isolation of human T follicular regulatory cells Basic Protocol 4: Measurement of human T follicular regulatory cell suppressive function.
调节性 T 细胞(Tregs)表达转录因子 Foxp3 对于控制免疫稳态具有关键作用。Treg 亚群滤泡辅助性 T 细胞(Tfr)具有专门的功能,可以迁移到 B 细胞滤泡并控制抗体反应。虽然 Tfr 可以通过其蛋白或基因表达谱来识别,但使用体外功能测定来确定其抑制能力对于进一步表征这些细胞非常重要。本文介绍了从人和小鼠中鉴定和纯化 Tfr 的方法,然后与 B 细胞和滤泡辅助性 T 细胞(Tfh)共培养。通过流式细胞术测量 Tfh 依赖性 B 细胞类别转换和浆母细胞形成的抑制活性以及通过酶联免疫吸附试验测量培养上清液中的免疫球蛋白产生来评估 Tfr 的抑制活性。这些测定还将提供对任何分离的 Tfr 或 Treg 群体的功能抑制能力的深入表征。©2021Wiley Periodicals LLC. 基本方案 1:分离小鼠 T 滤泡调节细胞 基本方案 2:测量小鼠 T 滤泡调节细胞抑制功能 基本方案 3:分离人 T 滤泡调节细胞 基本方案 4:测量人 T 滤泡调节细胞抑制功能。