Evidence map›Paper›PMID 42475880›Full record

ArticleEBioMedicine2026

Single-cell sequencing reveals NK cell dysregulation during chronic HIV infection and identifies transitional NK cell cytotoxicity related to HIV reservoir decay.

Wen-Jing Cao, Bao-Peng Yang, Si-Yuan Chen, Cheng Zhen, Xue-Meng Li, Xiang-Yi Cao, Lin-Yu Wan, Li-Ping Zhang, Mengyuan Zhang, Jia-Min Gao and 7 more

Abstract read
In one paragraph

Article in EBioMedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Wen-Jing CaoDepartment of Infectious Disease, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China; Department of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Bao-Peng YangDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Si-Yuan ChenDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Cheng ZhenDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Xue-Meng LiDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; Department of Clinical Medicine, Bengbu Medical University, Bengbu, Anhui, China.
Xiang-Yi CaoDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; Medical School, University of Chinese Academy of Sciences, Beijing, China.
Lin-Yu WanDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Li-Ping ZhangDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Mengyuan ZhangThe First School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Jia-Min GaoDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Chao ZhangDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Yan-Mei JiaoDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Xing FanDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Ruo-Nan XuDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Hui-Huang HuangDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China. Electronic address: hhh302@163.com.
Fu-Sheng WangDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China. Electronic address: fswang302@163.com.
Jin-Wen SongDepartment of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China. Electronic address: songjinwenchina@yeah.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural killer (NK) cells, as an integral component of the innate immune system, assume a pivotal role in combating viral infections. Our understanding of how human immunodeficiency virus (HIV) infection affects NK cell heterogeneity remains limited.

methodsWe conducted single-cell RNA sequencing (scRNA-seq) on peripheral blood NK cells from five healthy controls and seventeen male people living with HIV (PLWH), both before and after antiretroviral therapy (ART). Biological sex was extracted from medical records, and gender identity was not collected. O-link proteomic analysis was employed to quantify alterations in plasma inflammatory cytokines. Cell-associated HIV-DNA was measured in CD4

findingsAmong ten identified NK cell subsets, c7-Type I interferon (IFN)-responding cells were increased in untreated participants, correlating negatively with CD4

interpretationOur findings offer a comprehensive understanding of the cellular and molecular heterogeneity of NK cell immune response during HIV infection and offer insights for NK cell-based immunotherapies.

fundingSupported by grants from the National Natural Science Foundation of China (No. 82371766, 82572006, 82101837, and 82271857).

Indexed as

Cytotoxicity, ImmunologicHIV-1HIV InfectionsKiller Cells, NaturalSingle-Cell AnalysisAdultCD4-Positive T-LymphocytesChronic DiseaseCytokinesHumansMaleMiddle AgedProteomicsSingle-Cell Gene Expression AnalysisViral LoadCytokinesHIVHIV reservoirNK cellsscRNA-seq

Identifiers

PMID42475880
PMCPMC13393751

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.