Evidence mapPaperPMID 40211397Full record

ReviewEuropean journal of medical research2025

Host-directed therapy for tuberculosis.

Na Tian, Hongqian Chu, Qi Li, Hong Sun, Jingfang Zhang, Naihui Chu, Zhaogang Sun

Abstract readReview
In one paragraph

Review in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Epigenetic Reprogramming byAntibiotics (Basel, Switzerland) · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Recent advances in tuberculosis treatment: Towards shorter, safer, and more effective therapies.Journal of clinical tuberculosis and other mycobacterial diseases · 2026
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
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

7 authors.

Na Tian *Department of Tuberculosis, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, 101149, China.
Hongqian Chu *Translational Medicine Center, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China.
Qi LiDepartment of Tuberculosis, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, 101149, China.
Hong SunTranslational Medicine Center, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China.
Jingfang ZhangTranslational Medicine Center, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China.
Naihui ChuDepartment of Tuberculosis, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, 101149, China. dongchu1994@sina.com.
Zhaogang SunTranslational Medicine Center, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China. sunzhaogang@bjxkyy.cn.

Funding

National Natural Science Foundation of China No.82272347the Capital Health Research and Development of Special Fund No.2022-1G-2161
6 · The paper itself

Abstract

Current TB treatment regimens are hindered by drug resistance, numerous adverse effects, and long treatment durations, highlighting the need for 'me-better' treatment regimens. Host-directed therapy (HDT) has gained recognition as a promising approach in TB treatment. It allows the repurposing of existing drugs approved for other conditions and aims to enhance the effectiveness of existing anti-TB therapies, minimize drug resistance, decrease treatment duration, and adverse effects. By modulating the host immune response, HDT ameliorates immunopathological damage and improves overall outcomes by promoting autophagy, antimicrobial peptide production, and other mechanisms. It holds promise for addressing the challenges posed by multiple and extensively drug-resistant Mycobacterium tuberculosis strains, which are increasingly difficult to treat using conventional therapies. This article reviews various HDT candidates, including repurposed drugs, explores their underlying mechanisms such as autophagy promotion and inflammation reduction, while emphasizing their potential to improve TB treatment outcomes and outlining future research directions.

Indexed as

Antitubercular AgentsMycobacterium tuberculosisTuberculosisAutophagyDrug RepositioningHumansAntitubercular AgentsHost-directed therapyHost responseInfectious diseasesMycobacterium tuberculosisTuberculosis

Identifiers

PMID40211397
PMCPMC11987284

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.