Evidence map›Paper›PMID 42154776›Full record

ArticlePLOS global public health2026

Association of Human Cytomegalovirus exposure with tuberculosis disease in South African adults with presumptive tuberculosis.

Derrick Semugenze, Arthur Chiwaya, George William Kasule, James Sserubiri, Rose Nabatanzi, Byron W P Reeve, Zaida Palmer, Hridesh Mishra, Achilles Katamba, Alberto García-Basteiro and 4 more

Abstract read
In one paragraph

Article in PLOS global public health, 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

14 authors.

Derrick SemugenzeDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.ORCID https://orcid.org/0000-0001-7973-7109
Arthur ChiwayaDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Stellenbosch University, Cape Town, South Africa.
George William KasuleDepartment of Medical Microbiology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.ORCID https://orcid.org/0000-0002-2123-9614
James SserubiriDepartment of Medical Microbiology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.
Rose NabatanziDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.
Byron W P ReeveDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Stellenbosch University, Cape Town, South Africa.
Zaida PalmerDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Stellenbosch University, Cape Town, South Africa.
Hridesh MishraDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Stellenbosch University, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-8572-2736
Achilles KatambaClinical Epidemiology & Biostatistics Unit, Department of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.ORCID https://orcid.org/0000-0002-2347-4183
Alberto García-BasteiroCentro de Investigação em Saúde de Manhiça (CISM), Maputo, Mozambique, ISGlobal, Barcelona Centre for International Health Research, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Moses L JolobaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.
Grant TheronDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Stellenbosch University, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-9216-2415
Frank CobelensDepartment of Global Health and Amsterdam Institute for Global Health and Development, Amsterdam University Medical Centers Location University of Amsterdam, Amsterdam, The Netherlands.
Willy SsengoobaDepartment of Medical Microbiology, Makerere University College of Health Sciences Kampala, Kampala, Uganda.ORCID https://orcid.org/0000-0002-1643-110X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies suggested that human cytomegalovirus (HCMV) exposure may increase tuberculosis (TB) disease risk. We assessed the association between active HCMV infection and recent HCMV exposure with tuberculosis (TB) disease among TB-presumptive South African adults. This was a cross-sectional case-control study that utilized stored plasma and serum samples collected from adults (≥18 years) with presumptive TB self-presenting to primary care clinics in in the Kraaifontein District in Cape Town, South Africa. This study analyzed TB Cases (n = 98) who were mycobacterial culture and or GeneXpert Ultra positive and controls (n = 199) who were frequency matched by HIV status. Current HCMV infection (including reactivation or reinfection) and recent infection were defined using qPCR and serology (IgM and IgG avidity ELISA), while HCMV DNAemia was defined by a positive qPCR result alone. In a logistic regression model adjusting for age, gender, HIV status and BMI, TB disease was associated with HCMV DNAemia [adjusted odds ratio (aOR) 4.99, 95%CI 1.63-16.99, p = 0.007]. A similar association was observed for current HCMV infection, whereas no association was found for recent HCMV infection. These results indicate that active HCMV replication although not frequent may impair immune response to TB disease, TB disease could be leading to HCMV replication or an underlying common factor reactivates HCMV and Mtb replication in this population.

Identifiers

PMID42154776
PMCPMC13186327

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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.