ImmunoTechnology Section, Vaccine Research Center (VRC), National Institute of Allergy and Infectious Diseases, US National Institutes of Health (NIH), Bethesda, MD, USA.
Nat Protoc. 2013 Jan;8(1):33-42. doi: 10.1038/nprot.2012.143. Epub 2012 Dec 6.
The T cell compartment is phenotypically and functionally heterogeneous; subsets of naive and memory cells have different functional properties, and also differ with respect to homeostatic potential and the ability to persist in vivo. Human stem cell memory T (T(SCM)) cells, which possess superior immune reconstitution and antitumor response capabilities, can be identified by polychromatic flow cytometry on the basis of the simultaneous expression of several naive markers together with the memory marker CD95. We describe here a protocol based on the minimum set of markers required for optimal identification of human and nonhuman primate (NHP) T(SCM) cells with commonly available flow cytometers. By using flow sorters, T(SCM) cells can thereby be isolated efficiently at high yield and purity. With the use of the 5.5-h isolation procedure, depending on the number of cells needed, the sorting procedure can last for 2-15 h. We also indicate multiple strategies for their efficient expansion in vitro at consistent numbers for functional characterization or adoptive transfer experiments.
T 细胞群具有表型和功能异质性;幼稚细胞和记忆细胞亚群具有不同的功能特性,而且在稳态潜能和体内持久性方面也存在差异。人类干细胞记忆 T(T(SCM)) 细胞具有优越的免疫重建和抗肿瘤反应能力,可以通过多色流式细胞术基于同时表达几种幼稚标志物和记忆标志物 CD95 来识别。我们在这里描述了一种基于最小标记物集的方案,该方案可使用常用流式细胞仪对人类和非人类灵长类动物(NHP)T(SCM)细胞进行最佳识别。通过使用流式细胞分选器,可以高效、高纯度地分离 T(SCM)细胞。使用 5.5 小时的分离程序,根据所需细胞数量的不同,分选过程可持续 2-15 小时。我们还指出了多种在体外以一致数量进行有效扩增的策略,用于功能特征分析或过继转移实验。