Enhanced mitochondrial function in B cells from elderly type-2 diabetes mellitus patients supports intrinsic inflammation.

IF 3.3 Q2 GERIATRICS & GERONTOLOGY
Frontiers in aging Pub Date : 2024-08-23 eCollection Date: 2024-01-01 DOI:10.3389/fragi.2024.1444527
Daniela Frasca, Valquiria Bueno
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引用次数: 0

Abstract

In this paper, we measured B cell function in elderly healthy individuals (EH) and in elderly patients with Type-2 Diabetes Mellitus (T2DM, ET2DM), which are treatment-naive, as compared to healthy young (YH) individuals. Results show a higher serum inflammatory status of elderly versus young individuals, and especially of ET2DM versus EH. This status is associated with a reduced response to the seasonal influenza vaccine and with increased frequencies of the circulating pro-inflammatory B cell subset called Double Negative (DN) B cells. B cells from ET2DM patients are not only more inflammatory but also hyper-metabolic as compared to those from EH controls. The results herein are to our knowledge the first to show that T2DM superimposed on aging further increases systemic and B cell intrinsic inflammation, as well as dysfunctional humoral immunity. Our findings confirm and extend our previously published findings showing that inflammatory B cells are metabolically supported.

老年 2 型糖尿病患者 B 细胞线粒体功能增强支持内在炎症。
在本文中,我们测量了老年健康人(EH)和未接受治疗的老年 2 型糖尿病(T2DM,ET2DM)患者与健康年轻人(YH)相比的 B 细胞功能。结果显示,老年人的血清炎症状态高于年轻人,尤其是 ET2DM 患者的血清炎症状态高于 EH 患者。这种状态与对季节性流感疫苗的反应减弱以及循环中被称为双阴性(DN)B 细胞的促炎症 B 细胞亚群的频率增加有关。与 EH 对照组相比,ET2DM 患者的 B 细胞不仅更具炎症性,而且代谢也更旺盛。据我们所知,本文的研究结果首次表明,T2DM 与衰老叠加会进一步加剧全身和 B 细胞的内在炎症以及体液免疫功能失调。我们的研究结果证实并扩展了我们之前发表的研究结果,这些结果表明炎症性 B 细胞得到了新陈代谢的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.00
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0.00%
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审稿时长
13 weeks
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