The imbalance of CD4⁺Foxp3⁺ T cell subsets is reportedly involved in abnormal inflammatory immune responses in patients with chronic obstructive pulmonary disease (COPD). However, the possible role of CD4⁺CD25^-Foxp3⁺ T cells in immune regulation in COPD remains to be investigated. In the current study, distribution and phenotypic characteristics of CD4⁺CD25^-Foxp3⁺ T cells from peripheral blood were determined by flow cytometry; the origin, immune function and ultimate fate of CD4⁺CD25^-Foxp3⁺ T cells were further explored in vitro. It was observed that circulating CD4⁺CD25^-Foxp3⁺ T cells were significantly increased in stable COPD patients (SCOPD) and resembled central memory or effector memory T cells. Compared with peripheral CD4⁺CD25⁺Foxp3⁺ T cells, peripheral CD4⁺CD25^-Foxp3⁺ T cells showed a lower expression of Foxp3, CTLA-4, HELIOS, and TIGIT, but a higher expression of CD127 and KI-67, suggesting that CD4⁺CD25^-Foxp3⁺ T cells lost the expression of Tregs-associated molecules following the reduction in CD25. Unexpectedly, our study found that transforming growth factor-β1 (TGFβ1) decreased CD25 expression and played a critical role in the generation of CD4⁺CD25^-Foxp3⁺ T cells from CD4⁺CD25⁺Foxp3⁺ T cells. Phenotypic analysis further revealed that both inducible and peripheral CD4⁺CD25^-Foxp3⁺ T cells exhibited the features of activated conventional T cells. Importantly, memory CD4⁺CD25^-Foxp3⁺ T cells facilitated the proliferation and differentiation of naïve CD4⁺ T cells into Th17 cells in the presence of IL-1β, IL-6, IL-23, and TGFβ1. Finally, a fraction of CD4⁺CD25^-Foxp3⁺ T cells, exhibiting instability and plasticity, were converted to Th17 cells when subjected to Th17 cell-polarizing condition. Taken together, we propose that TGFβ1 is responsible for the generation of CD4⁺CD25^-Foxp3⁺ T cells, and these cells functionally exert an auxiliary effect on Th17 cells generation and might perpetuate chronic inflammation in COPD.

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