达沙替尼和槲皮素的抗衰老治疗不能改善老年小鼠的总体流感反应。

IF 3.3 Q2 GERIATRICS & GERONTOLOGY
Frontiers in aging Pub Date : 2023-06-16 eCollection Date: 2023-01-01 DOI:10.3389/fragi.2023.1212750
Blake L Torrance, Andreia N Cadar, Dominique E Martin, Hunter A Panier, Erica C Lorenzo, Jenna M Bartley, Ming Xu, Laura Haynes
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引用次数: 0

摘要

年龄是流感(流感)感染后不良后果的最大危险因素。随着年龄的增长,衰老细胞的负担增加已被确定为许多衰老疾病的根本原因,用称为抗衰老药的药物靶向这些细胞,在减轻许多与年龄相关的器官系统衰退方面显示出希望。然而,针对这些细胞是否会改善免疫系统中与年龄相关的缺陷,目前尚不清楚。在这里,我们使用了一种具有良好特征的抗衰老治疗,即达沙替尼和槲皮素(D + Q)的组合,以清除年龄(18-20个月)的小鼠在流感感染之前的衰老细胞。我们全面分析了原发性感染期间的免疫反应以及免疫记忆的发展和病原体再次遭遇后的保护。抗衰老治疗没有改善免疫反应的任何方面,包括:体重减轻、病毒载量、CD8 T细胞浸润、抗体产生、记忆T细胞发育或回忆能力。这些结果表明,D + Q可能不是一种适当的抗衰老药物,以提高老年人对流感感染的免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Senolytic treatment with dasatinib and quercetin does not improve overall influenza responses in aged mice.

Senolytic treatment with dasatinib and quercetin does not improve overall influenza responses in aged mice.

Senolytic treatment with dasatinib and quercetin does not improve overall influenza responses in aged mice.

Senolytic treatment with dasatinib and quercetin does not improve overall influenza responses in aged mice.

Age is the greatest risk factor for adverse outcomes following influenza (flu) infection. The increased burden of senescent cells with age has been identified as a root cause in many diseases of aging and targeting these cells with drugs termed senolytics has shown promise in alleviating many age-related declines across organ systems. However, there is little known whether targeting these cells will improve age-related deficits in the immune system. Here, we utilized a well characterized senolytic treatment with a combination of dasatinib and quercetin (D + Q) to clear aged (18-20 months) mice of senescent cells prior to a flu infection. We comprehensively profiled immune responses during the primary infection as well as development of immune memory and protection following pathogen reencounter. Senolytic treatment did not improve any aspects of the immune response that were assayed for including: weight loss, viral load, CD8 T-cell infiltration, antibody production, memory T cell development, or recall ability. These results indicate that D + Q may not be an appropriate senolytic to improve aged immune responses to flu infection.

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