Basic Science Program, SAIC-Frederick, Inc, Laboratory of Molecular Immunoregulation, Cancer Inflammation Program, NCI-Frederick, Frederick, Maryland 21702, United States.
Int Immunopharmacol. 2011 Oct;11(10):1489-96. doi: 10.1016/j.intimp.2011.05.018. Epub 2011 May 31.
Authenticating markers for the functional suppressive CD4(+)FoxP3(+) regulatory T cells (Tregs) are important for the quantitative identification and enrichment of viable Tregs for possible therapeutic use. CD25 as a surrogate marker of Tregs has some limitations, which prompted investigators to identify more specific marker(s) of Tregs. The search for a firm molecular definition of Tregs resulted in the identification of FoxP3 as a better marker of this subset of CD4 cells. Nevertheless, FoxP3(+) Tregs are phenotypically and functionally heterogeneous. Even in normal mice, only a minority of FoxP3(+) T cells are potent suppressor cells. Therefore, additional marker(s) are required for delineation of truly functional Tregs. In this review, the studies identifying markers of functional Tregs, both in mouse and in human, and their functional implications are discussed. Our finding that TNFR2, which mediates the effect of TNF on the activation of Tregs, is a superb marker of the most suppressive subset of mouse Tregs and its application in the identification of functional human Tregs will also be reviewed.
鉴定功能性抑制性 CD4(+)FoxP3(+)调节性 T 细胞(Tregs)的标记物对于定量鉴定和富集有活力的 Tregs 以用于可能的治疗用途非常重要。CD25 作为 Tregs 的替代标志物具有一些局限性,这促使研究人员寻找 Tregs 的更特异性标志物。对 Tregs 的明确分子定义的研究导致鉴定 FoxP3 作为 CD4 细胞这一亚群的更好标志物。然而,FoxP3(+)Tregs 在表型和功能上是异质的。即使在正常小鼠中,只有少数 FoxP3(+)T 细胞是有效的抑制细胞。因此,需要额外的标志物来描绘真正功能的 Tregs。在这篇综述中,我们讨论了在小鼠和人类中鉴定功能性 Tregs 标记物的研究,以及它们的功能意义。我们的发现表明,TNFR2 介导 TNF 对 Tregs 激活的作用,是小鼠 Tregs 中最具抑制性亚群的优秀标志物,其在鉴定功能性人类 Tregs 中的应用也将进行综述。