Frasca Daniela, Bueno Valquiria
Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, United States.
Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, United States.
Front Aging. 2024 Aug 23;5:1444527. doi: 10.3389/fragi.2024.1444527. eCollection 2024.
In this paper, we measured B cell function in elderly healthy individuals (E) and in elderly patients with Type-2 Diabetes Mellitus (T2DM, E), which are treatment-naive, as compared to healthy young (Y) individuals. Results show a higher serum inflammatory status of elderly versus young individuals, and especially of E versus E. 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 E patients are not only more inflammatory but also hyper-metabolic as compared to those from E 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.
在本文中,我们检测了老年健康个体(E组)和未经治疗的老年2型糖尿病患者(T2DM,E组)的B细胞功能,并与健康年轻个体(Y组)进行比较。结果显示,老年个体的血清炎症状态高于年轻个体,尤其是E组患者高于E组健康个体。这种状态与对季节性流感疫苗的反应降低以及循环中称为双阴性(DN)B细胞的促炎B细胞亚群频率增加有关。与E组健康对照者的B细胞相比,E组患者的B细胞不仅炎症性更强,而且代谢更活跃。据我们所知,本文的结果首次表明,叠加在衰老之上的2型糖尿病会进一步增加全身和B细胞内在炎症以及功能失调的体液免疫。我们的研究结果证实并扩展了我们之前发表的研究结果,即炎症性B细胞得到代谢支持。