Evidence map›Paper›PMID 24179111›Full record

Trial reportThe Journal of infectious diseases2014

Distinct T-cell responses when BCG vaccination is delayed from birth to 6 weeks of age in Ugandan infants.

F Lutwama, B M Kagina, A Wajja, F Waiswa, N Mansoor, S Kirimunda, E J Hughes, N Kiwanuka, M L Joloba, P Musoke and 4 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2014. 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
1.3field-weighted citation impact, top 20% 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, 38 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Bacillus Calmette-Guérin vaccination at birth and in vitro cytokine responses to non-specific stimulation. A randomized clinical trial.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Trial
  4. Trial
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Exploiting Pre-Existing CD4Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  11. Article
  12. Observational
  13. Polyfunctional CD4Frontiers in immunology · 2017
    Review
  14. Article
  15. Review
  16. Factors influencing innate immunity and vaccine responses in infancy.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  17. Article
  18. Article
  19. 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

14 authors at 5 institutions in 4 countries.

F LutwamaSouth African Tuberculosis Vaccine Initiative, Institute of Infectious Diseases and Molecular Medicine.
B M Kagina
A Wajja
F Waiswa
N Mansoor
S Kirimunda
E J Hughes
N Kiwanuka
M L Joloba
P Musoke
T J Scriba
H Mayanja-Kizza
C L Day
W A Hanekom
Makerere University · UGUniversity of Cape Town · ZAInfectious Diseases Institute · UGSouth African Tuberculosis Vaccine Initiative · ZATuBerculosis Vaccine Initiative · NL

Funding

Mechanisms of Immune Regulation in Mycobacterium Tuberculosis InfectionR01AI083156 · NIAID · UNIVERSITY OF CAPE TOWN · PI DAY, CHERYL LIANE · 2009 to 2012
$415k
NIAID NIH HHS R01 AI083156
6 · The paper itself

Abstract

backgroundIn Uganda, the tuberculosis vaccine BCG is administered on the first day of life. Infants delivered at home receive BCG vaccine at their first healthcare facility visit at 6 weeks of age. Our aim was to determine the effect of this delay in BCG vaccination on the induced immune response.

methodsWe assessed CD4(+) and CD8(+) T-cell responses with a 12-hour whole-blood intracellular cytokine/cytotoxic marker assay, and with a 6-day proliferation assay.

resultsWe enrolled 92 infants: 50 had received BCG vaccine at birth and 42 at 6 weeks of age. Birth vaccination was associated with (1) greater induction of CD4(+) and CD8(+) T cells expressing either interferon γ (IFN-γ) alone or IFN-γ together with perforin and (2) induction of proliferating cells that had greater capacity to produce IFN-γ, tumor necrosis factor α (TNF-α), and interleukin 2 together, compared with delayed vaccination.

conclusionsDistinct patterns of T-cell induction occurred when BCG vaccine was given at birth and at 6 weeks of age. We propose that this diversity might impact protection against tuberculosis. Our results differ from those of studies of delayed BCG vaccination in South Africa and the Gambia, suggesting that geographical and population heterogeneity may affect the BCG vaccine-induced T-cell response.

Indexed as

BCG VaccineCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCross-Sectional StudiesCytokinesFemaleHumansImmunization ScheduleImmunologic MemoryInfantInfant, NewbornMaleUgandaBCG VaccineCytokinesBCGbirthCD4+ and CD8+ T-cell responsesdelayedUgandavaccination

Identifiers

PMID24179111
PMCPMC6392474
OpenAlexW2165390713

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.