免疫学
FOXP3型
发病机制
白细胞介素-7受体
抗体
白细胞介素2受体
人口
医学
生物
T细胞
免疫系统
环境卫生
作者
Barbara Fazekas de St Groth,Erhua Zhu,Suzanne Asad,Loretta Lee
标识
DOI:10.1007/978-1-61737-979-6_17
摘要
Tregs are absolutely required for the maintenance of self tolerance in mouse and man. Major abnormalities in Treg number or function cause rare but fatal syndromes with autoimmune, allergic and inflammatory features. Whether subtle Treg abnormalities contribute to the pathogenesis of sporadic autoimmune, allergic and immunoinflammatory diseases in man remains controversial. Robust methods for identifying and isolating human Tregs in patients and healthy controls are essential if we are to understand their role in these increasingly common diseases. We have outlined below a flow cytometric technique to detect and isolate the entire human Treg population based on expression of CD4, CD25, and CD127. Use of a number of additional antibodies for defining subsets within the Treg compartment is described. For analysis, anti-Foxp3 can be added to the cocktail, but the necessity for fixation and permeabilisation may reduce the signal from other antibodies.
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