Interplay between microRNAs and TGF-β signaling in T cells: implications for Th9 differentiation and immune pathogenesis
Since the discovery of microRNAs (miRNAs) in 1993, they have been established as key post-transcriptional regulators of immune cell function. In particular, miRNAs have emerged as key modulators of CD4 + T cell activation and differentiation. Accumulating evidence indicates that miRNAs influence CD4 + T cell fate through modulating transforming growth factor β (TGF-β) signaling, which negatively regulates T helper (Th) 1 and Th2 cell differentiation, while promoting the generation of regulatory T (Treg) cells, Th17 as well as Th9 cells. Despite these advances, our understanding of specific roles of miRNAs and their target molecules in CD4 + T cells remains limited, particularly in Th9 cells. In this review, we discuss the regulatory networks of miRNAs targeting the TGF-β signaling pathway in CD4 + T cells, with a special focus on their roles in Th9 cell differentiation and function.
Authors
- T W Kim
- Yun-Ji Lim (ORCID: https://orcid.org/0000-0001-5885-5771)
Institutions
- National Institute of Dental and Craniofacial Research (US)
- Pusan National University Dental Hospital (KR)
- Pusan National University Yangsan Hospital (KR)
- Pusan National University (KR)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2026-05-01
- DOI
- https://doi.org/10.3389/fimmu.2026.1828634
- Primary Topic
- MicroRNA in disease regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00