Here we studied and characterized different peripheral blood (PB) regulatory T cell (Treg) subsets in rheumatoid arthritis (RA) patients and tested the hypothesis that changes in these cells can be linked to the degree of inflammation and relapsing/remission periods. PB cells were examined from RA subjects (n = 60) with different disease activity score-28 (DAS28) and from healthy controls (n = 40). Frequencies of Treg subsets expressing characteristic membrane antigens, FoxP3 or intracellular cytokines were quantified by flow cytometry. We observed a decrease in the percentages of CD4+CD25high, CD4+CD25int, CD4+CD25int/highFoxP3+, CD4+CD38+, CD4+CD62L+, CD8+CD25highCD45RA+ and CD8+CD25intCD45RA+ T cells in PB of RA patients compared to healthy controls. In addition, we found increased percentages of cells expressing membrane/intracellular regulatory antigens such as OX40 (CD134), CD45RBlow or CTLA-4 (CD152), and a higher proportion of other T cell subsets including CD4+CTLA-4+, CD4+IL10+, CD4+CD25intIL10+, CD4+CD25int TGFβ+, CD4+CD25low TGFβ+ and CD8+CD28− . We show that most of these changes parallel the intensity of inflammation, with lowest or highest values in patients with moderately/very active disease compared to healthy controls and at times to patients with inactive RA. The balance between these cell subsets and their antigen expression would determine the inflammation levels and could thus be linked to the relapsing/remission periods of the disease.