Evidence map›Paper›PMID 35428268›Full record

ArticleBMC infectious diseases2022

Cascade Immune Mechanisms of Protection against Mycobacterium tuberculosis (IMPAc-TB): study protocol for the Household Contact Study in the Western Cape, South Africa.

Andriёtte M Hiemstra, Candice E MacDonald, Ilana C van Rensburg, Kim Stanley, Elizna Maasdorp, Shirley Mc Anda, Susanne Tönsing, Jane Alexandra Shaw, Gerard Tromp, Gian D van der Spuy and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Lung Resident T Cells Across the Spectrum of TB Infection and Disease.bioRxiv : the preprint server for biology · 2026
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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

16 authors at 3 institutions in 2 countries.

Andriёtte M HiemstraBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa. ahiemstra@sun.ac.za.ORCID http://orcid.org/0000-0002-6331-9858
Candice E MacDonaldBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Ilana C van RensburgBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Kim StanleyBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Elizna MaasdorpDivision of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Stellenbosch University, Cape Town, South Africa.
Shirley Mc AndaBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Susanne TönsingBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Jane Alexandra ShawBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Gerard TrompDivision of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Stellenbosch University, Cape Town, South Africa.
Gian D van der SpuyDivision of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Stellenbosch University, Cape Town, South Africa.
Kevin B UrdahlSeattle Children's Research Institute, Seattle, USA.
David M LewinsohnDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, USA.
Helena KuivaniemiDivision of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Stellenbosch University, Cape Town, South Africa.
Nelita Du PlessisDivision of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Stellenbosch University, Cape Town, South Africa.
Stephanus T MalherbeBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
Gerhard WalzlBiomedical Research Institute Clinical Team, Stellenbosch University, Cape Town, South Africa.
South African Medical Research Council · ZAOregon Health & Science University · USUniversity of Washington · US

Funding

IMMUNE MECHANISMS OF PROTECTION AGAINST MYCOBACTERIUM TUBERCULOSIS CENTER (IMPAC-TB) - SARS-CoV-2 RELATED RESEARCH75N93019C00070 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI URDAHL, KEVIN · 2019 to 2025
$86.6M
Bill and Melinda Gates Foundation NuMeRi Node for Infection ImagingEuropean and Developing Countries Clinical Trials Partnership TMA2016CDF1576National Institute of Allergy and Infectious Diseases 75N93019C0070NIAID NIH HHS 75N93019C00070SANRF 86535South African Medical Research Council SHIP-SATBBI
6 · The paper itself

Abstract

backgroundNatural immunity against Mycobacterium tuberculosis exists, and > 90% of those infected remain disease-free. Innate and adaptive immune responses required to mediate such protection against tuberculosis (TB) are, however, poorly understood.

methodsThis is an analytical study exploring protective and non-protective pathways of immunity against Mycobacterium tuberculosis. Adults without HIV infection are recruited at community healthcare clinics in high TB incidence areas of the Western Cape Province, South Africa. Data regarding participants' medical, social and medication usage will be collected, and clinical examinations and point-of-care tests documented. Reference tests for TB (chest radiographs and sputum tests for GeneXpert MTB/RIF Ultra®, Auramine smear and liquid cultures) and investigations to classify infection states [interferon-gamma release assay (IGRA) and SARS-CoV-2 polymerase chain reaction (PCR) nasopharyngeal swab and IgG], are done on all participants who meet the inclusion criteria. 18F-Fluorodeoxyglucose positron emission tomography combined with computerized tomography will be done on all close contacts (contacts) and healthy control (controls) participants. Participants are divided into 12 study groups representing a spectrum of TB clinical phenotypes and prior SARS-CoV-2 infection based on their TB status, exposure history, results of IGRA test at baseline and 3 months, SARS-CoV-2 serology, and PCR results, and for contacts and controls, PET-CT imaging findings indicative of sub-clinical TB lesions. Samples for experimental assays include whole blood for isolation of peripheral blood mononuclear cells and blood in PAXgene® tubes for RNA isolation. All SARS-CoV-2 PCR negative study participants undergo bronchoscopy for collecting bronchoalveolar lavage samples. DISCUSSION: The paired blood and BAL samples will be used for comprehensive analyses of the tissue-specific and systemic immunity that will include e.g., cytometry by time-of-flight analyses, RNA-sequencing, multiplex immunoassays, epigenetic analysis, and mechanistic studies of control of infection by Mycobacterium tuberculosis. Results will be integrated with those from mice and non-human primate studies to provide a comprehensive analysis of protective pathways in natural and vaccine-induced immunity against Mycobacterium tuberculosis.

Indexed as

COVID-19HIV InfectionsMycobacterium tuberculosisTuberculosis, Lymph NodeAnimalsHumansLeukocytes, MononuclearMicePositron Emission Tomography Computed TomographyRNASARS-CoV-2South AfricaRNABronchoalveolar lavageHousehold contactsImmune responseInterferon-gamma release assayPET-CT imagingSARS-CoV-2Tuberculosis

Identifiers

PMID35428268
PMCPMC9012070
OpenAlexW4224043492

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.