Therapeutic potential of regulatory T cells for stem cell regulation: Insights from Treg-mediated enhancement of limbal stem cell functions

Regulatory T cells (Tregs) play a key role in immunomodulation and tissue regeneration. Limbal stem cells (LSCs) maintain corneal epithelial homeostasis, and LSC deficiency (LSCD) leads to visual impairment. Current LSCD treatments face donor shortages and graft rejection risks. The present study explored Tregs' therapeutic potential for LSCD in a mouse model of graded LSCD and further explored the direct effect of Tregs on LSCs function by <i>in vitro</i> coculturing human-derived cells. Subconjunctival Tregs injection effectively treated mild and moderate LSCD in mouse models. Coculturing human LSCs with human Tregs promoted LSCs migration, proliferation, and stemness maintenance. Furthermore, amphiregulin (AREG), secreted by Tregs, was crucial to their therapeutic effects, as AREG<sup>-/-</sup> Tregs resulted in diminished efficacy on LSCD mice compared to wild-type Tregs. These findings highlight Tregs as a promising treatment for LSCD, enhancing LSC function partially via AREG production.

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Journal
iScience
Published
2025-04-22
DOI
https://doi.org/10.1016/j.isci.2025.112515
Primary Topic
T-cell and B-cell Immunology
Type
article
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Therapeutic potential of regulatory T cells for stem cell regulation: Insights from Treg-mediated enhancement of limbal stem cell functions

Yao Fu, Chunyi Shao, Liangbo Chen, Junzhao Chen et al.
1 links
iScience
T-cell and B-cell Immunology
article

Therapeutic potential of regulatory T cells for stem cell regulation: Insights from Treg-mediated enhancement of limbal stem cell functions

Yao Fu, Chunyi Shao, Liangbo Chen, Junzhao Chen, Fei Fang, Tianyi Zhou, Shiding Li, A Tingxi
article en

Abstract

Regulatory T cells (Tregs) play a key role in immunomodulation and tissue regeneration. Limbal stem cells (LSCs) maintain corneal epithelial homeostasis, and LSC deficiency (LSCD) leads to visual impairment. Current LSCD treatments face donor shortages and graft rejection risks. The present study explored Tregs' therapeutic potential for LSCD in a mouse model of graded LSCD and further explored the direct effect of Tregs on LSCs function by <i>in vitro</i> coculturing human-derived cells. Subconjunctival Tregs injection effectively treated mild and moderate LSCD in mouse models. Coculturing human LSCs with human Tregs promoted LSCs migration, proliferation, and stemness maintenance. Furthermore, amphiregulin (AREG), secreted by Tregs, was crucial to their therapeutic effects, as AREG<sup>-/-</sup> Tregs resulted in diminished efficacy on LSCD mice compared to wild-type Tregs. These findings highlight Tregs as a promising treatment for LSCD, enhancing LSC function partially via AREG production.

iScienceVol. 28(5)
Shanghai Jiao Tong University (CN), Shanghai Ninth People's Hospital (CN), Shanghai Institute of Hematology (CN)
Openalex Percentile: Top 91%
T-cell and B-cell Immunology
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