Evidence map›Paper›PMID 32582177›Full record

Trial reportFrontiers in immunology2020

Limited Impact of Human Cytomegalovirus Infection in African Infants on Vaccine-Specific Responses Following Diphtheria-Tetanus-Pertussis and Measles Vaccination.

Momodou Cox, Jane U Adetifa, Fatou Noho-Konteh, Jainaba Njie-Jobe, Lady C Sanyang, Abdoulie Drammeh, Magdalena Plebanski, Hilton C Whittle, Sarah L Rowland-Jones, Iain Robertson and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

11 authors.

Momodou CoxInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Jane U AdetifaInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Fatou Noho-KontehInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Jainaba Njie-JobeInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Lady C SanyangInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Abdoulie DrammehInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Magdalena PlebanskiSchool of Health & Biomedical Science, RMIT University, Melbourne, VIC, Australia.
Hilton C WhittleInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Sarah L Rowland-JonesInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.
Iain RobertsonSchool of Medicine and School of Health Sciences, University of Tasmania, Launceston, TAS, Australia.
Katie L FlanaganInfant Immunology Group, Vaccines and Immunity Theme, MRC Unit, Fajara, Gambia.

Funding

Medical Research Council G0701291
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) infection has a profound effect on the human immune system, causing massive clonal expansion of CD8, and to a lesser extend CD4 T cells. The few human trials that have explored the effect of HCMV infection on responses to vaccination are conflicting, with some studies suggesting no effect whilst others suggest decreased or increased immune responses. Recent studies indicate substantial differences in overall immune system reactivity to vaccines based on age and sex, particularly cellular immunity. 225 nine-month old Gambian infants were immunized with diphtheria-tetanus-whole cell pertussis and/or measles vaccines. HCMV infection status was determined by the presence of CMV DNA by PCR of urine samples prior to vaccination. The effect of HCMV infection on either protective antibody immunity or vaccine-specific and overall cellular immune responses 4 weeks post-vaccination was determined, further stratified by sex. Tetanus toxoid-specific antibody responses were significantly lower in HCMV+ infants compared to their HCMV- counterparts, while pertussis, diphtheria and measles antibody responses were generally comparable between the groups. Responses to general T cell stimulation with anti-CD3/anti-CD28 as well as antigen-specific cytokine responses to purified protein derivative (PPD) were broadly suppressed in infants infected with HCMV but, perhaps surprisingly, there was only a minimal impact on antigen-specific cellular responses to vaccine antigens. There was evidence for subtle sex differences in the effects of HCMV infection, in keeping with the emerging evidence suggesting sex differences in homeostatic immunity and in responses to vaccines. This study reassuringly suggests that the high rates of HCMV infection in low income settings have little clinically significant impact on antibody and cellular responses to early life vaccines, while confirming the importance of sex stratification in such studies.

Indexed as

Antibodies, BacterialAntibodies, ViralCohort StudiesCytokinesCytomegalovirus InfectionsDiphtheria-Tetanus-Pertussis VaccineFemaleGambiaHumansImmune ToleranceImmunity, CellularImmunoglobulin GInfantMaleMeasles VaccineProspective StudiesAntibodies, BacterialAntibodies, ViralCytokinesDiphtheria-Tetanus-Pertussis VaccineImmunoglobulin GMeasles VaccineTetanus Toxoidantibodiescellular immunitydiphtheria-tetanus-pertussis (DTwP) vaccinationhuman cytomegalovirushuman infantsmeasles vaccinationvaccine responses

Identifiers

PMID32582177
PMCPMC7291605

What OpenQuestion holds

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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.