Phenotypical characterization of regulatory T cells in humans and rodents

被引:137
作者
Rodriguez-Perea, A. L. [1 ]
Arcia, E. D. [1 ]
Rueda, C. M. [2 ]
Velilla, P. A. [1 ]
机构
[1] Univ Antioquia UdeA, Fac Med, Grp Inmunovirol, Medellin, Colombia
[2] Cincinnati Childrens Hosp Med Ctr, Clin Lab, Canc & Blood Dis Inst, Cincinnati, OH 45229 USA
关键词
human; regulatory T cells; rodent; spleen and lymph nodes; DENDRITIC CELLS; IN-VITRO; FIXATION/PERMEABILIZATION BUFFER; FOXP3-EXPRESSING CD25(+); SUPPRESSIVE FUNCTION; CD127; EXPRESSION; FOXP3; HIGH-FREQUENCY; CUTTING EDGE; PROLIFERATION;
D O I
10.1111/cei.12804
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (T-regs) constitute a fascinating subpopulation of CD4(+) T cells due to their ability to limit the immune response against self and non-self antigens. Murine models and antibodies directed against surface and intracellular molecules have allowed elucidation of the mechanisms that govern their development and function. However, these markers used to their classification lack of specificity, as they can be expressed by activated T cells. Similarly, there are slight differences between animal models, in steady state and pathological conditions, anatomical localization and strategy of analysis by flow cytometry. Here, we revised the most common markers utilized for T-reg typification by flow cytometry such as CD25, forkhead box protein 3 (FoxP3) and CD127, along with our data obtained in different body compartments of humans, mice and rats. Furthermore, we revised and determined the expression of other molecules important for the phenotypical characterization of T-reg cells. We draw attention to the drawbacks of those markers used in chronic states of inflammation. However, until a specific marker for the identification of T-regs is discovered, the best combination of markers will depend upon the tissue or the degree of inflammation from which T-regs derive.
引用
收藏
页码:281 / 291
页数:11
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