Viro-Immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Blegdamsvej 9B, DK-2100, Copenhagen Ø, Denmark.
Department of Cardiology, The Heart Center, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
BMC Infect Dis. 2022 May 11;22(1):451. doi: 10.1186/s12879-022-07450-y.
Monocytes play an important role in inflammation, and monocytosis and monocyte activation are features of chronic inflammation. We aimed to investigate if HIV status was associated with monocyte count and monocyte activation and to assess the relationship between monocyte count and monocyte activation markers and HIV-related factors.
Persons living with HIV (PLWH) with measured monocyte count and sCD14 and sCD163 were included from the Copenhagen Comorbidity in HIV infection (COCOMO) study and matched 1:5 on sex and age with uninfected controls. In addition, 74 uninfected individuals from COCOMO with measured sCD14 and sCD163 were included. Identical protocols and equipment were used to determine monocyte counts and monocyte activation in PLWH and uninfected controls. Linear regression adjusted for age, sex, smoking and waist-to-hip-ratio was used to analyze the association between possible risk factors and monocyte outcomes.
We included 871 PLWH and 4355 uninfected controls. PLWH had - 0.021 [- 0.031 - 0.011] × 10/L) lower monocyte count than uninfected controls, and in adjusted analyses HIV status was independently associated with - 0.035 [- 0.045, - 0.025] × 10/L lower monocyte count. In contrast, PLWH had higher sCD163 and sCD14 concentrations than uninfected controls. After adjustment, HIV-status was associated with higher sCD14 and sCD163 concentrations (588 [325, 851] ng/ml, and 194 [57, 330] ng/ml, respectively).
PLWH had lower monocyte counts than controls, but the absolute difference was small, and any clinical impact is likely limited. In contrast, concentrations of monocyte activation markers, previously implicated as drivers of non-AIDS comorbidity, were higher in PLWH than in controls.
单核细胞在炎症中起着重要作用,单核细胞增多症和单核细胞激活是慢性炎症的特征。我们旨在研究 HIV 状态是否与单核细胞计数和单核细胞激活有关,并评估单核细胞计数与单核细胞激活标志物与 HIV 相关因素之间的关系。
从哥本哈根 HIV 感染合并症(COCOMO)研究中纳入了有测量单核细胞计数和可溶性 CD14(sCD14)及可溶性 CD163(sCD163)的 HIV 感染者(PLWH),并按性别和年龄与未感染对照 1:5 匹配。此外,还纳入了来自 COCOMO 的 74 名未感染的个体,他们有测量的 sCD14 和 sCD163。相同的方案和设备用于确定 PLWH 和未感染对照的单核细胞计数和单核细胞激活。使用线性回归调整年龄、性别、吸烟和腰臀比,分析可能的危险因素与单核细胞结果之间的关系。
我们纳入了 871 名 PLWH 和 4355 名未感染对照。PLWH 的单核细胞计数比未感染对照低 -0.021(-0.031 至-0.011)×10/L,在调整分析中,HIV 状态与单核细胞计数低 -0.035(-0.045 至-0.025)×10/L 独立相关。相反,PLWH 的 sCD163 和 sCD14 浓度高于未感染对照。调整后,HIV 状态与 sCD163 和 sCD14 浓度较高相关(分别为 588[325,851]ng/ml 和 194[57,330]ng/ml)。
PLWH 的单核细胞计数低于对照,但绝对差异较小,可能具有有限的临床影响。相反,单核细胞激活标志物的浓度在 PLWH 中高于对照,这些标志物以前被认为是导致非艾滋病合并症的驱动因素。