Sharma Amit, Sharma Garima, Im Sin-Hyeog
Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Innovation Research Center for Bio-Future Technology (B-IRC), Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Gut Microbes. 2025 Dec;17(1):2516702. doi: 10.1080/19490976.2025.2516702. Epub 2025 Jun 15.
The establishment and maintenance of immune homeostasis rely on a dynamic, bidirectional exchange of information between commensal microorganisms and the host immune system. At the center of this process are CD4Foxp3 regulatory T cells (Tregs), which have emerged as pivotal mediators to ensure immunological equilibrium. This review explores the sophisticated mechanisms by which the gut microbiota modulates the differentiation, expansion, and functional specialization of Tregs, orchestrating intestinal immune tolerance to support host-microbiota mutualism. We discuss the role of microbial-derived structural components and metabolites in shaping the immunoregulatory fitness of Tregs. Additionally, we explore the impact of gut microbial dysbiosis, where disrupted microbial-immune crosstalk compromises immune tolerance, contributing to the development of inflammatory and autoimmune disorders. Finally, we highlight the potential of microbiota-based strategies to recalibrate intestinal immunity and restore immune tolerance.
免疫稳态的建立和维持依赖于共生微生物与宿主免疫系统之间动态的双向信息交换。这一过程的核心是CD4Foxp3调节性T细胞(Tregs),它们已成为确保免疫平衡的关键介质。本综述探讨了肠道微生物群调节Tregs分化、扩增和功能特化的复杂机制,协调肠道免疫耐受以支持宿主-微生物群共生关系。我们讨论了微生物衍生的结构成分和代谢产物在塑造Tregs免疫调节适应性方面的作用。此外,我们探讨了肠道微生物群失调的影响,其中微生物-免疫串扰的破坏会损害免疫耐受,导致炎症和自身免疫性疾病的发展。最后,我们强调了基于微生物群的策略在重新校准肠道免疫和恢复免疫耐受方面的潜力。