Mesenchymal stromal cells induce regulatory Tcells via epigenetic conversion of human conventional CD4 Tcells in vitro

Autor: Azevedo, Rita I., Minskaia, Ekaterina, Fernandes‐Platzgummer, Ana, Vieira, Ana I. S., da Silva, Cláudia L., Cabral, Joaquim M. S., Lacerda, João F.
Zdroj: Stem Cells; August 2020, Vol. 38 Issue: 8 p1007-1019, 13p
Abstrakt: Regulatory T cells (Treg) play a critical role in immune tolerance. The scarcity of Treg therapy clinical trials in humans has been largely due to the difficulty in obtaining sufficient Treg numbers. We performed a preclinical investigation on the potential of mesenchymal stromal cells (MSCs) to expand Treg in vitro to support future clinical trials. Human peripheral blood mononuclear cells from healthy donors were cocultured with allogeneic bone marrow‐derived MSCs expanded under xenogeneic‐free conditions. Our data show an increase in the counts and frequency of CD4+CD25highFoxp3+CD127lowTreg cells (4‐ and 6‐fold, respectively) after a 14‐day coculture. However, natural Treg do not proliferate in coculture with MSCs. When purified conventional CD4 T cells (Tcon) are cocultured with MSCs, only cells that acquire a Treg‐like phenotype proliferate. These MSC‐induced Treg‐like cells also resemble Treg functionally, since they suppress autologous Tcon proliferation. Importantly, the DNA methylation profile of MSC‐induced Treg‐like cells more closely resembles that of natural Treg than of Tcon, indicating that this population is stable. The expression of PD‐1 is higher in Treg‐like cells than in Tcon, whereas the frequency of PDL‐1 increases in MSCs after coculture. TGF‐β levels are also significantly increased MSC cocultures. Overall, our data suggest that Treg enrichment by MSCs results from Tcon conversion into Treg‐like cells, rather than to expansion of natural Treg, possibly through mechanisms involving TGF‐β and/or PD‐1/PDL‐1 expression. This MSC‐induced Treg population closely resembles natural Treg in terms of phenotype, suppressive ability, and methylation profile. Coculture in vitro of purified human conventional CD4 T cells (Tcon) with mesenchymal stromal cells (MSCs) induces a population of regulatory T cells (Treg). MSC‐induced Treg (iTreg) express CD25 and Foxp3, proliferate in culture, suppress Tcon proliferation such as fresh Treg, and display low levels of DNA methylation in CAMTA1, more closely resembling fresh Treg than the Tcon they arose from.
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