Kruize Zita, Maurer Irma, van Dort Karel A, van den Elshout Mark A M, Hoornenborg Elske, Booiman Thijs, Prins Maria, Kootstra Neeltje A
Department of Experimental Immunology, Amsterdam UMC, Amsterdam Infection & Immunity Institute, University of Amsterdam, Amsterdam, the Netherlands.
Department of Infectious Diseases, Research and Prevention, Public Health Service of Amsterdam, Amsterdam, the Netherlands.
Open Forum Infect Dis. 2020 Jul 5;7(8):ofaa284. doi: 10.1093/ofid/ofaa284. eCollection 2020 Aug.
We recently reported that the levels of activation, exhaustion, and terminal differentiation within the peripheral T-cell compartment were increased in men who have sex with men (MSM) compared with blood bank donors. During activation and differentiation, T cells undergo metabolic changes to maintain their energy demand.
The effect of cytomeglovirus (CMV) infection and risk behavior on the immune phenotype of peripheral T cells and the immune bioenergy metabolism profile in human immunodeficiency virus-negative MSM (with high or low sexual risk behavior) and blood bank donors was evaluated.
Men who have sex with men exhibited increased levels of T-cell activation and terminal differentiation and an impairment of the bioenergy metabolism (mitochondrial respiration and glycolysis) compared with blood bank donors. Cytomeglovirus infection was associated with increased terminal differentiation of CD4 (B = 3.41; 95% confidence interval [CI], 1.98-4.85; < .0001) and CD8 T cells (CD57: B = 1.21, 95% CI = 0.41-2.02, = .004; CD27CD28: B = 2.20, 95% CI = 1.21-3.18, < .0001; and CD57 of CD28: B = 1.02, 95% CI = 0.38-1.66, = .002) and increased glycolysis (B = 0.97; 95% CI, 0.27-1.67; = .007). Risk behavior was associated with increase activation of CD4 T cells (B = 0.22; 95% CI, 0.07-0.37; = .005), increased terminal differentiation of CD4 (B = 0.82; 95% CI, 0.44-1.20; < .0001) and CD8 T cells (B = 1.55; 95% CI, 0.58-2.51; = .002), and decreased glycolysis (glycolysis: B = -0.40, 95% CI = -0.68 to 0.12, = .006; and glycolytic capacity: B = -0.54, 95% CI = -0.91 to 0.16, = .005).
Men who have sex with men show an increased prevalence of bloodborne and sexually transmitted infection, indicating that immunological changes in the T-cell population and the bioenergy metabolism observed in MSM can most likely be attributed to chronic antigen exposure.
我们最近报告称,与血库捐献者相比,男男性行为者(MSM)外周T细胞区室中的激活、耗竭和终末分化水平有所增加。在激活和分化过程中,T细胞会发生代谢变化以维持其能量需求。
评估了巨细胞病毒(CMV)感染和风险行为对人类免疫缺陷病毒阴性的MSM(有高或低性风险行为)和血库捐献者外周T细胞免疫表型及免疫生物能量代谢谱的影响。
与血库捐献者相比,男男性行为者表现出T细胞激活和终末分化水平增加以及生物能量代谢(线粒体呼吸和糖酵解)受损。巨细胞病毒感染与CD4(B = 3.41;95%置信区间[CI],1.98 - 4.85;P <.0001)和CD8 T细胞的终末分化增加相关(CD57:B = 1.21,95% CI = 0.41 - 2.02,P =.004;CD27CD28:B = 2.20,95% CI = 1.21 - 3.18,P <.0001;以及CD28的CD57:B = 1.02,95% CI = 0.38 - 1.66,P =.002)和糖酵解增加(B = 0.97;95% CI,0.27 - 1.67;P =.007)。风险行为与CD4 T细胞激活增加(B = 0.22;95% CI,0.07 - 0.37;P =.005)、CD4(B = 0.82;95% CI,0.44 - 1.20;P <.0001)和CD8 T细胞终末分化增加(B = 1.55;95% CI,0.58 - 2.51;P =.002)以及糖酵解减少相关(糖酵解:B = -0.40,95% CI = -0.68至0.12,P =.006;以及糖酵解能力:B = -0.54,95% CI = -0.91至0.16,P =.005)。
男男性行为者血源和性传播感染的患病率增加,表明在男男性行为者中观察到的T细胞群体免疫变化和生物能量代谢很可能归因于慢性抗原暴露。