Evidence map›Paper›PMID 33661925›Full record

ArticlePLoS genetics2021

Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations.

Jocelyn Quistrebert, Marianna Orlova, Gaspard Kerner, Le Thi Ton, Nguyễn Trong Luong, Nguyễn Thanh Danh, Quentin B Vincent, Fabienne Jabot-Hanin, Yoann Seeleuthner, Jacinta Bustamante and 12 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
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  11. Review
  12. Article
  13. Article
  14. Article
  15. Association study betweenFrontiers in oncology · 2023
    Article
  16. Antibiotic Resistance toAntibiotics (Basel, Switzerland) · 2022
    Review
  17. Article
  18. Review
  19. Phenotype Definition for "Resisters" toFrontiers in immunology · 2021
    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

22 authors at 9 institutions in 5 countries.

Jocelyn QuistrebertLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0002-4973-3235
Marianna OrlovaInfectious Diseases and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montreal, Canada.ORCID 0000-0002-8108-938X
Gaspard KernerLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0003-0146-9428
Le Thi TonCenter for Social Disease Control, Binh Duong, Vietnam.
Nguyễn Trong LuongCenter for Social Disease Control, Binh Duong, Vietnam.
Nguyễn Thanh DanhCenter for Social Disease Control, Binh Duong, Vietnam.
Quentin B VincentLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.
Fabienne Jabot-HaninBioinformatics Core Facility, Paris Descartes University, Paris, France.ORCID 0000-0001-9294-7135
Yoann SeeleuthnerLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.
Jacinta BustamanteLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.
Stéphanie Boisson-DupuisSt Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York City, New York, United States of America.
Nguyen Thu HuongHospital for Dermato-Venereology, Ho Chi Minh City, Vietnam.
Nguyen Ngoc BaHospital for Dermato-Venereology, Ho Chi Minh City, Vietnam.
Jean-Laurent CasanovaLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0002-7782-4169
Christophe DelacourtUniversity of Paris, Imagine Institute, Paris, France.ORCID 0000-0002-0007-7150
Eileen G HoalSouth African Medical Research Council Centre for Tuberculosis Research, DST-NRF Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID 0000-0002-6444-5688
Alexandre AlcaïsLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0002-1012-2226
Vu Hong ThaiHospital for Dermato-Venereology, Ho Chi Minh City, Vietnam.
Lai The ThànhCenter for Social Disease Control, Binh Duong, Vietnam.
Laurent AbelLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0001-7016-6493
Erwin SchurrInfectious Diseases and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montreal, Canada.ORCID 0000-0002-2640-536X
Aurélie CobatLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Paris, France.ORCID 0000-0001-7209-6257
Inserm · FRHCMC Hospital of Dermato Venereology · VNMcGill University Health Centre · CACentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRHoward Hughes Medical Institute · USRockefeller University · USSouth African Medical Research Council · ZAUniversité Paris Cité · FR

Funding

CIHR FDN-143332
6 · The paper itself

Abstract

The natural history of tuberculosis (TB) is characterized by a large inter-individual outcome variability after exposure to Mycobacterium tuberculosis. Specifically, some highly exposed individuals remain resistant to M. tuberculosis infection, as inferred by tuberculin skin test (TST) or interferon-gamma release assays (IGRAs). We performed a genome-wide association study of resistance to M. tuberculosis infection in an endemic region of Southern Vietnam. We enrolled household contacts (HHC) of pulmonary TB cases and compared subjects who were negative for both TST and IGRA (n = 185) with infected individuals (n = 353) who were either positive for both TST and IGRA or had a diagnosis of TB. We found a genome-wide significant locus on chromosome 10q26.2 with a cluster of variants associated with strong protection against M. tuberculosis infection (OR = 0.42, 95%CI 0.35-0.49, P = 3.71×10-8, for the genotyped variant rs17155120). The locus was replicated in a French multi-ethnic HHC cohort and a familial admixed cohort from a hyper-endemic area of South Africa, with an overall OR for rs17155120 estimated at 0.50 (95%CI 0.45-0.55, P = 1.26×10-9). The variants are located in intronic regions and upstream of C10orf90, a tumor suppressor gene which encodes an ubiquitin ligase activating the transcription factor p53. In silico analysis showed that the protective alleles were associated with a decreased expression in monocytes of the nearby gene ADAM12 which could lead to an enhanced response of Th17 lymphocytes. Our results reveal a novel locus controlling resistance to M. tuberculosis infection across different populations.

Indexed as

Chromosomes, Human, Pair 10Genetic Predisposition to DiseaseGenome-Wide Association StudyMycobacterium tuberculosisQuantitative Trait LociAllelesComputational BiologyDisease ResistanceFranceGenotypeHumansMeta-Analysis as TopicPopulation GroupsSouth AfricaTuberculosisVietnam

Identifiers

PMID33661925
PMCPMC7963100
OpenAlexW3134413622

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.