CD4+CD25+CD127dimFoxp3+T cells are cytotoxic for human neurons

Activated human CD4+CD25+CD127dimFoxp3+T cells induce severe neurotoxicity while having no suppressive activity and secreting interferon‐γ and granzyme B. MS lesions are characterized by destruction of myelin and significant neuronal and axonal loss. Preliminary studies with the use of Tregsin the mouse model of MS have been extremely encouraging. However, recent studies with human cells have shown the presence of different subpopulations of T cells within the CD4+CD25+Foxp3+T cell phenotype, some of which do not have regulatory functions. These findings suggest a potential difference between mouse and human in the regulatory phenotype. Here, we show that human activated CD4+CD25+Foxp3+T cells are neurotoxic in vitro. These cells expressed high levels of the cytotoxic molecule GrB and had no suppressive effect. On the contrary, they produced IFN‐γ and low IL‐17, suggesting a shift toward a TH1 phenotype. Thus, our data confirm the presence of a nonregulatory cytotoxic subpopulation within the human CD4+CD25+Foxp3+T cells and suggest further studies on the human regulatory phenotype prior to any potential therapeutic application.