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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Interplay between microRNAs and TGF-β signaling in T cells: implications for Th9 differentiation and immune pathogenesis

T W Kim, Yun-Ji Lim
Frontiers in Immunology
MicroRNA in disease regulation
article

Interplay between microRNAs and TGF-β signaling in T cells: implications for Th9 differentiation and immune pathogenesis

T W Kim, Yun-Ji Lim
article en

Abstract

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.

Frontiers in ImmunologyVol. 17
National Institute of Dental and Craniofacial Research (US), Pusan National University Dental Hospital (KR), Pusan National University Yangsan Hospital (KR), Pusan National University (KR)
Openalex Percentile: Top 10%
MicroRNA in disease regulation
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Interplay between microRNAs and TGF-β signaling in T cells: implications for Th9 differentiation and immune pathogenesis — T W Kim, Yun-Ji Lim · Frontiers in Immunology (2026) | TGRS Research Map | TGRS