Evidence map›Paper›PMID 14737096›Full record

ArticleGenes and immunity2004

Genetic regulation of immune responses to vaccines in early life.

M J Newport, T Goetghebuer, H A Weiss, H Whittle, C-A Siegrist, A Marchant, MRC Gambia Twin Study Group

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

99 citing papers in PubMed, 207 citations in OpenAlex.

  1. Trial
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  7. Human genetics of responses to vaccines.Clinical and experimental immunology · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Vaccinomics and adversomics: key elements for a personalized vaccinology.Clinical and experimental vaccine research · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Personalized health and the coronavirus vaccines-Do individual genetics matter?BioEssays : news and reviews in molecular, cellular and developmental biology · 2021
    Review

39 more citing papers are in PubMed but not listed here.

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

7 authors at 6 institutions in 3 countries.

M J NewportDepartment of Medicine, University of Cambridge, UK. melanie.newport@cimr.cam.ac.uk
T Goetghebuer
H A Weiss
H Whittle
C-A Siegrist
A Marchant
MRC Gambia Twin Study Group
University of Geneva · CHJohn Radcliffe Hospital · GBLondon School of Hygiene & Tropical Medicine · GBMedical Research Council · GBMRC Unit the Gambia · GMUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infant immunization is the most cost-effective strategy to prevent infectious diseases in childhood, but is limited by immaturity of the immune system. To define strategies to improve vaccine immunogenicity in early life, the role of genetic and environmental factors in the control of vaccine responses in infant twins was studied. Immune responses to BCG, polio, hepatitis B, diphtheria, pertussis and tetanus vaccines were measured at 5 months of age in 207 Gambian twin pairs recruited at birth. Intrapair correlations for monozygous and dizygous pairs were compared to estimate the environmental and genetic components of variation in responses. High heritability was observed for antibody (Ab) responses to hepatitis B (77%), oral polio (60%), tetanus (44%) and diphtheria (49%) vaccines. Significant heritability was also observed for interferon-gamma and interleukin-13 responses to tetanus, pertussis and some BCG vaccine antigens (39-65%). Non-HLA genes played a dominant role in responses to Ab-inducing vaccines, whereas responses to BCG were predominantly controlled by genes within the HLA class II locus. Genetic factors, particularly non-HLA genes, significantly modulate immune responses to infant vaccination. The identification of the specific genes involved will provide new targets for the development of vaccines and adjuvants for young infants that work independently of HLA.

Indexed as

Models, GeneticBCG VaccineDiphtheria-Tetanus-Pertussis VaccineEnzyme-Linked Immunosorbent AssayGambiaGenes, MHC Class IHepatitis B VaccinesHumansImmunity, ActiveImmunoglobulin GInfantInterferon-gammaInterleukin-13Linear ModelsPoliovirus Vaccine, OralTwinsBCG VaccineDiphtheria-Tetanus-Pertussis VaccineHepatitis B VaccinesImmunoglobulin GInterferon-gammaInterleukin-13Poliovirus Vaccine, Oral

Identifiers

PMID14737096
OpenAlexW1979329174

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.