Evidence map›Paper›PMID 38809023›Full record

ArticleMicrobiology spectrum2024

Immunoinhibitory effects of anti-tuberculosis therapy induce the host vulnerability to tuberculosis recurrence.

Isha Pahuja, Antara Ghoshal, Ahmed Abdallah Okieh, Akanksha Verma, Kriti Negi, Meetu Agarwal, Nidhi Subhash Chandra, Saurabh Kumar Sharma, Ashima Bhaskar, Ved Prakash Dwivedi

Abstract read
In one paragraph

Article in Microbiology spectrum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Pathogens (Basel, Switzerland) · 2026
    Article
  2. Review
  3. 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

10 authors.

Isha PahujaImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.ORCID 0009-0002-1893-551X
Antara GhoshalImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Ahmed Abdallah OkiehImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Akanksha VermaImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Kriti NegiImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Meetu AgarwalDepartment of Molecular Medicine, Jamia Hamdard University, New Delhi, India.
Nidhi Subhash ChandraDepartment of Microbiology, Ram Lal Anand College, University of Delhi, New Delhi, India.
Saurabh Kumar SharmaSchool of Computer & Systems Sciences, Jawaharlal Nehru University, New Delhi, India.
Ashima BhaskarImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.ORCID 0000-0002-7367-874X
Ved Prakash DwivediImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.ORCID 0000-0003-4321-2567

Funding

Department of Science and Technology, Ministry of Science and Technology, India (DST) ND/DST/15/024DST | Science and Engineering Research Board (SERB) ND/DST/16/023DST | Science and Engineering Research Board (SERB) ND/DST/23/034
6 · The paper itself

Abstract

The host immune responses play a pivotal role in the establishment of long-term memory responses, which effectively aids in infection clearance. However, the prevailing anti-tuberculosis therapy, while aiming to combat tuberculosis (TB), also debilitates innate and adaptive immune components of the host. In this study, we explored how the front-line anti-TB drugs impact the host immune cells by modulating multiple signaling pathways and subsequently leading to disease relapse. Administration of these drugs led to a reduction in innate immune activation and also the cytokines required to trigger protective T cell responses. Moreover, these drugs led to activation-induced cell death in the mycobacterial-specific T cell leading to a reduced killing capacity. Furthermore, these drugs stalled the T cell differentiation into memory subsets by modulating the activation of STAT3, STAT4, FOXO1, and NFκB transcription factors and hampering the Th1 and Th17-mediated long-term host protective memory responses. These findings suggest the urgent need to augment directly observed treatment, short-course (DOTS) therapy with immunomodulatory agents to mitigate the adverse effects linked to the treatment.IMPORTANCEAs a central component of TB eradication initiatives, directly observed treatment, short-course (DOTS) therapy imparts immune-dampening effects during the course of treatment. This approach undermines the host immune system by delaying the activation process and lowering the immune response. In our investigation, we have unveiled the impact of DOTS on specific immune cell populations. Notably, the signaling pathways involving STAT3 and STAT4 critical for memory responses and NFκβ associated with pro-inflammation were substantially declined due to the therapy. Consequently, these drugs exhibit limited effectiveness in preventing recurrence of the disease. These observations highlight the imperative integration of immunomodulators to manage TB infection.

Indexed as

Antitubercular AgentsCytokinesMycobacterium tuberculosisTuberculosisAnimalsFemaleHumansImmunity, InnateImmunologic MemoryMiceMice, Inbred C57BLRecurrenceSignal TransductionTh17 CellsTh1 CellsAntitubercular AgentsCytokinesDOTSdrugsrecurrenceT cell memoryTuberculosis

Identifiers

PMID38809023
PMCPMC11218458

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.