Evidence map›Paper›PMID 42495612›Full record

ReviewFrontiers in immunology2026

Immunotherapy for tuberculosis: emerging modalities, cross-disciplinary innovations, and roadmaps for drug-resistant disease.

Junchi Xu, JunHeng Shen, Sufang Chen, Jie Chen, Xuanmiao Liu, Fei Gao, Jianping Zhang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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
–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

0 citing papers in PubMed.

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

7 authors.

Junchi Xu *Department of clinical laboratory, The Affiliated Infectious Diseases Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, China.
JunHeng Shen *Department of clinical laboratory, Suzhou Hospital of Traditional Chinese Medicinel, Suzhou, Jiangsu, China.
Sufang Chen *Department of clinical laboratory, The Affiliated Infectious Diseases Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, China.
Jie ChenDepartment of clinical Laboratory, Children's Hospital of Soochow University, Suzhou, Jiangsu, China.
Xuanmiao LiuDepartment of clinical Laboratory, Xi'an Daxing Hospital, Xi'an, Shaanxi, China.
Fei GaoDepartment of clinical Laboratory, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou, Jiangsu, China.
Jianping ZhangDepartment of clinical laboratory, The Affiliated Infectious Diseases Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale: The emergence of multidrug-resistant tuberculosis (MDR-TB) and limitations of current antibiotic therapies highlight the urgent need for novel treatment strategies. While immunotherapy has revolutionized cancer treatment, its potential in TB remains underexplored, with existing reviews focusing narrowly on vaccines and phage therapy. A comprehensive synthesis of TB immunotherapy advancements is critical to guide clinical translation. Content: Tuberculosis (TB) has been recognized as one of the earliest diseases treated with immunotherapy. The BCG vaccine played a crucial role in controlling TB epidemics for a long period. However, progress in TB immunotherapy stagnated due to the attenuation of BCG strains and the long-standing neglect in TB immunology research. In recent years, advances in TB and immunology research, including novel immunological theories such as trained immunity, alongside breakthroughs in various immunotherapies for cancer treatment, have provided new perspectives for TB treatment. This review summarizes the immune response to TB, including roles of macrophages, T cells, and nonclassical immune cells. It evaluates progress in cell therapy, antibody therapy, microbial therapy, vaccines, and cytokine therapy. Clinical trials, mechanisms, and challenges (e.g., immune exhaustion, antigen heterogeneity) of TB immunotherapy are analyzed, drawing parallels with cancer immunotherapy. Conclusions: Immunotherapy offers multifaceted strategies to overcome

Indexed as

ImmunotherapyMycobacterium tuberculosisTuberculosis, Multidrug-ResistantAnimalsAntitubercular AgentsHost-Directed TherapyHumansAntitubercular Agentsclinical trialsdrug-resistantimmunotherapytuberculosisvaccine

Identifiers

PMID42495612
PMCPMC13391292

What Socratic holds

Textmetadata
LicenceCC BY
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.