Single-cell sequencing of peripheral blood mononuclear cells reveals immune landscape of monkeypox patients with HIV

被引:1
作者
Liu, Yamin [1 ]
Liu, Xinhua [2 ]
Wang, Jingjing [3 ,4 ]
Xie, Ying [3 ,4 ]
Guo, Jing [3 ,4 ]
Liu, Zhiqiang [3 ,4 ]
Li, Ying [1 ]
Jiang, Bei [1 ]
Wang, Jingya [5 ]
机构
[1] Tianjin Second Peoples Hosp, Tianjin Inst Hepatol, Tianjin, Peoples R China
[2] Hangzhou Normal Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Hangzhou, Peoples R China
[3] Shandong First Med Univ, Shandong Canc Hosp & Inst, Shandong Prov Key Lab Precis Oncol, Jinan, Peoples R China
[4] Shandong Acad Med Sci, Jinan, Peoples R China
[5] Tianjin Med Univ, Dept Physiol & Pathophysiol, State Key Lab Expt Hematol, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Monkeypox; HIV; single-cell RNA sequencing; immune response; antiviral innate immunity; DENDRITIC CELLS; INFECTION; TARGETS; NEUTROPHILS; MECHANISMS; CD83;
D O I
10.1080/22221751.2025.2459136
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The monkeypox (MPXV) outbreak in 2022 is more prevalent among individuals with human immunodeficiency virus (HIV). While it is plausible that HIV-induced immunosuppression could result in a more severe progression, the exact mechanisms remain undetermined. To better understand the immunopathology of MPXV in patients with and without HIV infection, we employed single-cell RNA sequencing (scRNA-seq) to analyse peripheral blood mononuclear cells (PBMCs) from six patients hospitalized for MPXV, three of whom had HIV infection (HIV antibody positive and HIV RNA level below the detection limit), and three patients only infected with MPXV (HIV-). We map the peripheral immune response in both the acute phase and the recovery period, showing the reconfiguration of peripheral immune cell phenotypes in acute stage compared with recovery stage, characterized by disturbed cell subsets and intense cell interactions mediated by monocytes and neutrophils. Importantly, we also found obviously dysregulated gene expression and cell subsets in HIV+ patients proposing mechanism underlying their serious condition. Our findings provide a comprehensive cell atlas of MPXV patients, shed light on the mechanisms underlying the severe disease progression and longer recovery time in HIV+ individuals.
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页数:17
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