To ensure reliable Treg-cell rather than Th17-cell generation,

we added RA as a regulator to our culture conditions [45]. The synergistic effect of RA on the TGF-β-mediated Foxp3 induction has been reported previously [46-48]. The stability of in vitro induced Treg cells CB-839 clinical trial by addition of TGF-β, RA and IL-2 has been investigated previously. Prinz and colleagues demonstrated that these Treg cells lost their functionality in vivo and did not protect from GvHD [49]. Also, other groups reported that Foxp3 expression is lost when Treg cells were restimulated with TGF-β in the absence of IL-2 [50]. Foxp3 expression could not be reinduced when TGF-β was added again [51]. In our experimental setting, the addition of TGF-β and RA was used in combination with a nondepleting anti-CD4 antibody, which may explain the increased stability and in vivo function of our aTreg cells. Interestingly, RORγt but not IL-17 expression was increased in aCD4+TGF-β+RA aTreg cells (Fig. 1C). STAT3 activated by IL-6 and IL-23, which drive TH17 differentiation,

plays an important role for IL-17 production [52-54]. Indeed RA negatively influences the stability and maturation of Th17 cells by preventing IL-23 expression [55]. RA induces a Th2 response and thereby blocks a Th1 response [56]. Accordingly, this website all-trans RA rather induces Th2-related genes such as GATA-3 or c-maf, whereas Th1-related genes such as t-bet or IL-12Rβ2 are reduced [57]. Indeed, we detected a significant reduction of t-bet transcription in aCD4+TGF-β+RA aTreg cells (Fig. 1C). However, this had already been observed for aCD4 Treg cells. We could replicate the Th1-inhibiting potential of RA as not only aCD4+TGF-β+RA aTreg cells but also aCD4+Rapa aTreg cells produced less Th1 cytokines IFN-γ or TNF-α during primary Methane monooxygenase stimulation or upon restimulation (Fig. 2A and B). This effect could be observed for Foxp3+ aTreg cells as well as for residual Foxp3− T effector cells. Although addition of TGF-β+RA to the anti-CD4 antibody

treatment could increase the number of Foxp3+ cells generated out of CD4+CD25− cells, the obtained frequency was much lower as compared with that of cultures with whole CD4+ T cells. Therefore, we assume that our culture conditions predominantly favour the expansion of nTreg cells. It has been described that nTreg cells and iTreg cells can be distinguished by Helios [9]. However, Akimova et al. demonstrated that some effector T cells express Helios without expressing Foxp3 after TCR stimulation [10]. Zabransky et al. induced Helios in naïve sorted T cells in vitro depending on the strength of TCR stimulation and addition of TGF-β and IL-2, showing that Helios expression is not restricted to nTreg cells [58]. In our setting, 60% of freshly isolated CD4+CD25+Foxp3+ nTreg cells expressed Helios.