Transforming growth factor‑β2 increases the capacity of retinal pigment epithelial cells to induce the generation of regulatory T cells.

The present study investigated the underlying mechanism of the induction of regulatory T cells (Tregs) by retinal pigment epithelial (RPE) cells and the characteristics of these Tregs. Human RPE cells were cultured in the presence or absence of transforming growth factor-beta 2 (TGF-beta 2), and reverse-transcription quantitative PCR was performed to determine the mRNA expression of indoleamine 2,3-dioxygenase (IDO) and nuclear factor erythroid 2-related factor (Nrf2). Supernatants of RPE cell cultures were added to CD4(+) T cells to induce Tregs. The RPE-induced Tregs were purified by two-step magnetic cell sorting. The natural Tregs were isolated from the peripheral blood mononuclear cells of healthy volunteers. Purified CD4+ CD25-T cells (2x10(5)/well) were cultured alone or with Tregs (various densities, natural or RPE-induced). The proliferation of CD4(+) CD25-T cells was determined by 3H-thymidine incorporation. After 24 h of stimulation with TGF-beta 2, the mRNA expression of IDO in RPE cells was upregulated. The highest level of IDO mRNA expression was reached after 72 h of stimulation with TGF-beta 2. However, the Nrf2 mRNA expression was slightly decreased after 24 h of stimulation with TGF-beta 2 and significantly increased after 48-72 h of TGF-beta 2 stimulation. Increased levels of CD25 expression were observed on CD4(+) T cells exposed to supernatants of RPE cell cultures treated with TGF-beta 2 and recombinant interleukin-2. The RPE-induced Tregs were more effective at suppressing the proliferation of CD4(+) CD25-T cells compared with native Tregs. These findings suggested that IDO may be a signaling protein in RPE cells which is implicated in the induction of Tregs. RPE-induced Tregs have the potential to be applied for immunotherapy for ocular inflammatory diseases.