Evidence map›Paper›PMID 39198909›Full record

ArticleEuropean journal of medical research2024

Single-cell transcriptome sequencing reveals altered peripheral blood immune cells in patients with severe tuberculosis.

Li Wang, Ya He, Peng Wang, Hai Lou, Haipeng Liu, Wei Sha

Abstract read
In one paragraph

Article in European journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed.

  1. Discovery and validation of novel plasma protein biomarkers for severe tuberculosis patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Article
  3. Recent Characterization of Key Proteins to Combat Tuberculosis.Advances in experimental medicine and biology · 2026
    Review
  4. Article
  5. Article
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

6 authors.

Li Wang *Clinic and Research Center of Tuberculosis, School of Medicine, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China.
Ya He *Clinic and Research Center of Tuberculosis, School of Medicine, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China.
Peng Wang *Clinic and Research Center of Tuberculosis, School of Medicine, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China.
Hai LouClinic and Research Center of Tuberculosis, School of Medicine, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China.
Haipeng LiuCentral Laboratory, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China. haipengliu@tongji.edu.cn.
Wei ShaClinic and Research Center of Tuberculosis, School of Medicine, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China. 13671758200@126.com.

Funding

National Key R&D Program of China 2023YFC2307300Shanghai 2020 "science and technology innovation action plan" technological innovation fund:Clinical Study on New Short-Course treatment regimens and Host-Directed Therapy for MDR-TB 20Z11900500Shanghai Clinical Research Center for infectious disease (tuberculosis) 19MC1910800Shanghai key clinical specialty construction project-Tuberculosis department Shslczdzc03001Shanghai three-year (2023-2025) action plan to strengthen the public health system GWVI-11.1-05Shanghai three-year (2023-2025) action plan to strengthen the public health system GWVI-9
6 · The paper itself

Abstract

Tuberculosis is a serious global health burden, resulting in millions of deaths each year. Several circulating cell subsets in the peripheral blood are known to modulate the host immune response to Mycobacterium tuberculosis (Mtb) infection in different ways. However, the characteristics and functions of these subsets to varying stages of tuberculosis infection have not been well elucidated. Peripheral blood immune cells (PBICs) were isolated from healthy donors (HD group), individuals with mild tuberculosis (MI group), and individuals with severe tuberculosis (SE group). CD4+ naive T cells and CD8+ T cells were decreased in the SE and MI groups, while CD14+ monocytes were increased in the SE group. Further analysis revealed increased activated CD4+ T cells, transitional CD8+ T cells, memory-like NK cells, and IGHG3

Indexed as

TuberculosisAdultCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHumansKiller Cells, NaturalMaleMiddle AgedMonocytesMycobacterium tuberculosisSingle-Cell AnalysisTranscriptomeCD8+ T cellImmune cellScRNA-seqSevere tuberculosisTuberculosis

Identifiers

PMID39198909
PMCPMC11360321

What OpenQuestion holds

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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 OpenQuestion graph.