Evidence map›Paper›PMID 40901996›Full record

ArticlePloS one2025

Activation and proliferation profiles of M.tuberculosis specific dual functional CD4+T cells from smear negative pulmonary TB patients.

Ahmed Esmael, Adane Mihret, Tamrat Abebe, Daniel Mussa, Sebsib Neway, Joel Ernst, Jyothi Rengarajan, Liya Wassie, Rawleigh Howe

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ahmed EsmaelArmauer Hansen Research Institute, Addis Ababa, Ethiopia.ORCID https://orcid.org/0000-0002-0310-0280
Adane MihretArmauer Hansen Research Institute, Addis Ababa, Ethiopia.
Tamrat AbebeDepartment of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Ethiopia.
Daniel MussaArmauer Hansen Research Institute, Addis Ababa, Ethiopia.
Sebsib NewayArmauer Hansen Research Institute, Addis Ababa, Ethiopia.ORCID https://orcid.org/0000-0002-2033-5874
Joel ErnstDivision of Experimental Medicine, University of California San Francisco, San Francisco, California, United States of America.
Jyothi RengarajanDepartment of Medicine, Division of Infectious Diseases and Emory Vaccine Center, Emory University School of Medicine, Emory University, Atlanta, GeorgiaUnited States of America.
Liya WassieDepartment of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Ethiopia.
Rawleigh HoweDepartment of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Ethiopia.

Funding

Emory/Georgia TB Research Advancement Center (TRAC)P30AI168386 · NIAID · EMORY UNIVERSITY · PI Jeffrey M Collins · 2022 to 2026
$5.8M
Ethiopia-Emory TB Research Training ProgramD43TW009127 · FIC · EMORY UNIVERSITY · PI HENRY M BLUMBERG, Kidist Bobosha · 2013 to 2026
$3.4M
FIC NIH HHS D43 TW009127NIAID NIH HHS P30 AI168386
6 · The paper itself

Abstract

backgroundTuberculosis is a major public health challenge in the resource-limited endemic setting of sub-Saharan Africa. The diagnostic challenge becomes worse for smear-negative TB cases. Even if efforts for non-sputum-based TB diagnostic and prognostic biomarkers, there was limited data on blood-based immunological biomarkers among smear-negative PTB patients.Therefore, we assessed the phenotypic profile (HLA-DR, CD-38, Ki-67) of M. tuberculosis specific CD4 + T cells expressing dual IFN-γ and TNF-α cytokines from smear negative PTB patients in Addis Ababa, Ethiopia. METHODOLOGY: An institutional-based longitudinal cohort study was conducted in Addis Abeba, Ethiopia, on new smear-negative PTB who were adult and HIV-negative in comparison with multiple comparator groups. A total of 149 (confirmed patients with non-TB respiratory disease -33, smear-negative TB-29, smear-positive TB-34, apparently healthy - 53) study participants was enrolled. The expression level of activation (HLA-DR, CD-38) and proliferation (Ki-67) markers from dual IFN-γ and TNF-α cytokines expressing PPD specific CD4 + T cells were assessed after surface and intracellular cytokine staining. To confirm the presence of M. tuberculosis, MGIT/LJ culture, PCR, and smear microscopy were performed.

resultThe overall level of HLA-DR and CD-38 expression in smear-negative and positive pulmonary TB patients were substantially higher than that of confirmed non-TB respiratory illness, apparently healthy QFT positive and negative study participants (p-value = 0.0127, p-value < 0.0001, p-value = 0.0043, p-value <0.0001, respectively) before commencing anti TB treatment. Also, among the smear-negative and positive pulmonary TB cohort, the expression of CD-38, HLA-DR, and HLA-DR + CD-38 + expression was reduced in the second month and six-month cohort compared with baseline data (p-value= < 0.0001, p-value = 0.00365, p -value = 0.0001, respectively).

conclusionIn this study, we found the diagnostic and prognostic potential of activation markers, particularly CD-38, in smear-negative PTB patients from dual M. tuberculosis-specific IFN-γ + TNF-α+ cytokine producing CD4 + T cells in both the presumed ex vivo and antigen-specific stimulation assays.

Indexed as

CD4-Positive T-LymphocytesMycobacterium tuberculosisTuberculosis, PulmonaryAdultBiomarkersCell ProliferationEthiopiaFemaleHLA-DR AntigensHumansInterferon-gammaLongitudinal StudiesLymphocyte ActivationMaleMiddle AgedTumor Necrosis Factor-alphaBiomarkersHLA-DR AntigensInterferon-gammaTumor Necrosis Factor-alpha

Identifiers

PMID40901996
PMCPMC12407538

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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.