Morales-Sánchez Abigail, Lavaert Marieke, Vacchio Melanie S, Martinez-Ruiz Gustavo Ulises, Egbase Daniel, Zhao Yongge, Lake Ross, Ishikawa Masaki, Braikia Fatima Zohra, Jankovic Dragana, Sen Ranjan, Bosselut Rémy, Bhandoola Avinash, Cowan Jennifer E
National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Children's Hospital of Mexico Federico Gomez, Mexico City, Mexico.
PLoS Biol. 2025 Jul 28;23(7):e3003283. doi: 10.1371/journal.pbio.3003283. eCollection 2025 Jul.
Age-related thymic involution leads to diminished output of naïve T-cells. While this process is suggested to increase the risk of disease severity in the elderly following infection, direct evidence is lacking. We developed two mouse models that allow us to experimentally prevent or reverse thymic involution. Constitutive Myc expression in thymic epithelial cells (TEC) of middle-aged mice enhanced thymic function, and increased numbers of peripheral naïve CD4 and CD8 T-cells. Inducible Myc expression reversed age-related thymic involution and partially recovered peripheral naïve T-cell numbers. Importantly, improving thymic function in these settings preserved T-cell-dependent antibody responses and significantly reduced T-cell-associated mortality after infection with Toxoplasma gondii. Improved thymic function also rebalanced age-associated alterations in the Treg pool, and mitigated loss of the transcriptional Th1 signature in aged conventional T-cells. Our findings support the value of TEC-focused thymic regeneration strategies for enhancement of T-cell-mediated immunity in the elderly.
与年龄相关的胸腺退化导致幼稚T细胞输出减少。虽然这一过程被认为会增加老年人感染后疾病严重程度的风险,但缺乏直接证据。我们开发了两种小鼠模型,使我们能够通过实验预防或逆转胸腺退化。中年小鼠胸腺上皮细胞(TEC)中组成型Myc表达增强了胸腺功能,并增加了外周幼稚CD4和CD8 T细胞的数量。可诱导的Myc表达逆转了与年龄相关的胸腺退化,并部分恢复了外周幼稚T细胞数量。重要的是,在这些情况下改善胸腺功能可保留T细胞依赖性抗体反应,并显著降低感染刚地弓形虫后的T细胞相关死亡率。改善胸腺功能还可重新平衡Treg库中与年龄相关的改变,并减轻老年常规T细胞中转录Th1特征的丧失。我们的研究结果支持了以TEC为重点的胸腺再生策略在增强老年人T细胞介导免疫方面的价值。