衰老
肠道菌群
促炎细胞因子
失调
细胞毒性T细胞
细胞生物学
炎症
免疫系统
生物
免疫学
生物化学
体外
作者
Manuel M. Gómez de las Heras,Elisa Carrasco,Mario Pérez-Manrique,Naohiro Inohara,Sandra Delgado-Pulido,Álvaro Fernández-Almeida,María I. Gálvez-Castaño,Isaac Francos-Quijorna,Carolina Simó,Virginia García‐Cañas,José Ignacio Escrig-Larena,Juan Aranda,Gonzalo Soto‐Heredero,Enrique Gabandé‐Rodríguez,Eva María Blanco,Irma Joyce Dias de Almeida,Gabriel Núñez,Marı́a Mittelbrunn
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2025-08-01
卷期号:10 (110)
标识
DOI:10.1126/sciimmunol.adv0985
摘要
Healthy aging relies on a symbiotic host-microbiota relationship. The age-associated decline of the immune system can pose a threat to this delicate equilibrium. In this work, we investigated how the functional deterioration of T cells can affect host-microbiota symbiosis and gut barrier integrity and the implications of this deterioration for inflammaging, senescence, and health decline. Using the Tfam fl/fl Cd4 Cre mouse model, we found that T cell failure compromised gut immunity leading to a decrease in T follicular cells and regulatory T cells (T reg cells) and an accumulation of highly proinflammatory and cytotoxic T cells. These alterations were associated with intestinal barrier disruption and gut dysbiosis. Microbiota depletion or adoptive transfer of total CD4 T cells or a T reg cell–enriched pool prevented gut barrier dysfunction and mitigated premature inflammaging and senescence, ultimately enhancing the health span in this mouse model. Thus, a competent CD4 T cell compartment is critical to ensure healthier aging by promoting host-microbiota mutualism and gut barrier integrity.
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