Abstract
It has been known for decades that circulating human CD4 cells can express functional MHC class II molecules that induce T cell nonresponsiveness with Ag presentation. Because there is significant expression of MHC class II (MHC-II) determinants (DR) on a subpopulation CD4 ؉ CD25 high regulatory T cells (Treg), we examined the function of CD4 cells expressing MHC-DR. We demonstrate that MHC-II expression on human CD4 ؉ CD25 high T cells identifies a functionally distinct population of Treg that induces early contact-dependent suppression that is associated with high Foxp3 expression. In striking contrast, MHC-II ؊ CD4 ؉ CD25 high Treg induce early IL-4 and IL-10 secretion and a late Foxp3-associated contact-dependent suppression. The DR expressing CD25 high Treg express higher levels of Foxp3 message and protein, compared with the DR ؊ CD25 high Treg population. Direct single-cell cloning of CD4 ؉ CD25 high Treg revealed that, regardless of initial DR expression, ex vivo expression of CD25 high , and not DR, predicted which clones would exhibit contact-dependent suppression, high levels of Foxp3 message, and an increased propensity to become constitutive for DR expression. Thus, the direct ex vivo expression of MHC-II in the context of CD25 high
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CITATION STYLE
Swiatek-de Lange, M., Rist, W., Stahl, H. F., Weith, A., & Lenter, M. C. (2008). Comment on “MHC Class II Expression Identifies Functionally Distinct Human Regulatory T Cells.” The Journal of Immunology, 180(6), 3625–3625. https://doi.org/10.4049/jimmunol.180.6.3625
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