Evidence map›Paper›PMID 30333506›Full record

ArticleScientific reports2018

Age-related waning of immune responses to BCG in healthy children supports the need for a booster dose of BCG in TB endemic countries.

Elizabeth Whittaker, Mark P Nicol, Heather J Zar, Nontobeko G Tena-Coki, Beate Kampmann

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
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  6. Article
  7. Article
  8. Frontiers in immunology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Tuberculosis in times of COVID-19.Journal of epidemiology and community health · 2022
    Article
  18. Article
  19. 100 years of Mycobacterium bovis bacille Calmette-Guérin.The Lancet. Infectious diseases · 2022
    Review
  20. Article
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

5 authors.

Elizabeth WhittakerAcademic Department of Paediatrics, St Marys Campus, Imperial College London, 2nd Floor Wright-Fleming Building, Norfolk Place, London, W2 1PG, UK. e.whittaker@imperial.ac.uk.
Mark P NicolDivision of Medical Microbiology, Department of Pathology And Institute of Infectious Disease and Molecular Medicine UCT Faculty of Health Sciences, Observatory, 7925, South Africa.
Heather J ZarMRC Unit of Child & Adolescent Health, University of Cape Town, Rondebosch, Cape Town, 7701, South Africa.
Nontobeko G Tena-CokiDepartment of Paediatrics & Child Health, Red Cross War Memorial Children's Hospital, Klipfontein Road, Rondebosch, Cape Town, 7701, South Africa.
Beate KampmannAcademic Department of Paediatrics, St Marys Campus, Imperial College London, 2nd Floor Wright-Fleming Building, Norfolk Place, London, W2 1PG, UK.

Funding

Diagnosis of Tuberculosis in HIV-infected children & development of microbiologicR01HD058971 · NICHD · UNIVERSITY OF CAPE TOWN · PI ZAR, HEATHER JOY · 2008 to 2012
$2.2M
Department of Health SRF-2009-02-07Medical Research Council MC_EX_MR/K011944/1Medical Research Council MC_EX_MR/P024270/1Medical Research Council MC_UP_A900_1122Medical Research Council MC_UU_00026/2NICHD NIH HHS R01 HD058971Wellcome Trust
6 · The paper itself

Abstract

In the absence of a more effective vaccine against TB and in the interest of developing one, it is essential to understand immune responses associated with BCG protection. We comprehensively characterized T cell populations in BCG-vaccinated children over time. Blood from 78 healthy, BCG-vaccinated children representing four age groups (<1 yr, ≥1 yr <2 yr, ≥2 yr <5 yr, ≥5 yr), was stimulated in vitro for 24 hours and 6 days with live BCG to induce effector and central memory responses. Antigen-specific CD4, CD8, γδ and regulatory T cell populations were phenotyped and intracellular and secreted cytokines measured by flow cytometry and multiplex ELISA respectively. Our results demonstrated that populations of naïve T cells predominated in infants, compared to older children. However, BCG-specific effector CD4 T cell responses were equivalent and antigen-specific CD4 T cell proliferative capacity was increased in infants compared to older children. Increases in innate immune responses including γδ T cell responses and secreted pro-inflammatory cytokines were noted with increasing age. In conclusion, we identified that the capacity to expand and differentiate effector T cells in response to BCG stimulation wanes with increasing age, which may indicate waning central memory immunity. Booster vaccination could be considered to maintain the antigen-specific central memory pool and possibly enhance the duration of protection.

Indexed as

Age FactorsBCG VaccineCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildChild, PreschoolCytokinesHumansImmunologic MemoryInfantMycobacterium tuberculosisTime FactorsT-Lymphocytes, RegulatoryTuberculosisVaccinationBCG VaccineCytokines

Identifiers

PMID30333506
PMCPMC6193026

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.