Evidence map›Paper›PMID 38740997›Full record

ArticleNature medicine2024

High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response.

Alexander J Mentzer, Alexander T Dilthey, Martin Pollard, Deepti Gurdasani, Emre Karakoc, Tommy Carstensen, Allan Muhwezi, Clare Cutland, Amidou Diarra, Ricardo da Silva Antunes and 36 more

Abstract read
In one paragraph

Article in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–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

17 citing papers in PubMed.

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  16. Complex genetic variation in nearly complete human genomes.bioRxiv : the preprint server for biology · 2024
    Article
  17. 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

46 authors.

Alexander J MentzerCentre for Human Genetics, University of Oxford, Oxford, UK. alexander.mentzer@ndm.ox.ac.uk.ORCID 0000-0002-4502-2209
Alexander T DiltheyCentre for Human Genetics, University of Oxford, Oxford, UK.
Martin PollardWellcome Sanger Institute, Cambridge, UK.ORCID 0000-0001-8738-0920
Deepti GurdasaniWellcome Sanger Institute, Cambridge, UK.ORCID 0000-0001-9996-6929
Emre KarakocWellcome Sanger Institute, Cambridge, UK.
Tommy CarstensenWellcome Sanger Institute, Cambridge, UK.
Allan MuhweziMedical Research Council/Uganda Virus Research Institute and London School of Hygiene & Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Clare CutlandSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Amidou DiarraGroupe de Recherche Action en Santé (GRAS) 06 BP 10248, Ouagadougou, Burkina Faso.
Ricardo da Silva AntunesCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0001-9785-5272
Sinu PaulCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.
Gaby SmitsNational Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0003-4890-0940
Susan WareingMicrobiology Department, John Radcliffe Hospital, Oxford University NHS Foundation Trust, Oxford, UK.
HwaRan KimHistogenetics, New York, USA.
Cristina PomillaWellcome Sanger Institute, Cambridge, UK.
Amanda Y ChongCentre for Human Genetics, University of Oxford, Oxford, UK.ORCID 0000-0003-4919-2632
Debora Y C BrandtDepartment of Integrative Biology, University of California at Berkeley, California, CA, USA.ORCID 0000-0002-9565-7835
Rasmus NielsenDepartment of Integrative Biology, University of California at Berkeley, California, CA, USA.ORCID 0000-0003-0513-6591
Samuel NeavesAvon Longitudinal Study of Parents and Children at University of Bristol, Bristol, UK.
Nicolas TimpsonPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-7141-9189
Austin CrinklawCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.
Cecilia S Lindestam ArlehamnCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0001-7302-8002
Anna RautanenCentre for Human Genetics, University of Oxford, Oxford, UK.
Dennison KizitoMedical Research Council/Uganda Virus Research Institute and London School of Hygiene & Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Tom ParksCentre for Human Genetics, University of Oxford, Oxford, UK.
Kathryn AucklandCentre for Human Genetics, University of Oxford, Oxford, UK.
Kate E ElliottCentre for Human Genetics, University of Oxford, Oxford, UK.
Tara MillsCentre for Human Genetics, University of Oxford, Oxford, UK.
Katie EwerThe Jenner Institute, University of Oxford, Oxford, UK.ORCID 0000-0001-9827-9836
Nick EdwardsThe Jenner Institute, University of Oxford, Oxford, UK.ORCID 0000-0002-7030-7839
Segun FatumoMedical Research Council/Uganda Virus Research Institute and London School of Hygiene & Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Emily WebbMRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine London, London, UK.
Sarah PeacockTissue Typing Laboratory, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Katie JefferyMicrobiology Department, John Radcliffe Hospital, Oxford University NHS Foundation Trust, Oxford, UK.ORCID 0000-0002-6506-2689
Fiona R M van der KlisNational Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Pontiano KaleebuMedical Research Council/Uganda Virus Research Institute and London School of Hygiene & Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Pandurangan VijayanandCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0001-7067-9723
Bjorn PetersCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0002-8457-6693
Alessandro SetteCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0001-7013-2250
Nezih CerebHistogenetics, New York, USA.
Sodiomon SirimaGroupe de Recherche Action en Santé (GRAS) 06 BP 10248, Ouagadougou, Burkina Faso.ORCID 0000-0002-0972-4211
Shabir A MadhiSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.ORCID 0000-0002-7629-0636
Alison M ElliottMedical Research Council/Uganda Virus Research Institute and London School of Hygiene & Tropical Medicine Uganda Research Unit, Entebbe, Uganda.ORCID 0000-0003-2818-9549
Gil McVeanBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK.ORCID 0000-0002-5012-4162
Adrian V S Hill *Centre for Human Genetics, University of Oxford, Oxford, UK.ORCID 0000-0003-0900-9629
Manjinder S Sandhu *Department of Epidemiology & Biostatistics, School of Public Health, Imperial College London, London, UK. m.sandhu@imperial.ac.uk.ORCID 0000-0002-2725-142X

Funding

Single-cell atlas of lung tissue-resident memory T cells reactive to upper and lower respiratory tract pathogensU19AI118626 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Gregory Seumois · 2015 to 2026
$36.7M
Identifying mechanisms and correlates of long-lasting vaccine-induced immunity to whooping coughU01AI141995 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI PETERS, BJOERN, SETTE, ALESSANDRO · 2019 to 2023
$4.1M
Academy of Medical Sciences SGL024\1096Medical Research Council 217065/Z/19/ZMedical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009NIAID NIH HHS U01 AI141995NIAID NIH HHS U19 AI118626Wellcome TrustWellcome Trust 202802/Z/16/ZWellcome Trust 203141/Z/16/ZWellcome Trust (Wellcome) 106289/Z/14/Z
6 · The paper itself

Abstract

How human genetic variation contributes to vaccine effectiveness in infants is unclear, and data are limited on these relationships in populations with African ancestries. We undertook genetic analyses of vaccine antibody responses in infants from Uganda (n = 1391), Burkina Faso (n = 353) and South Africa (n = 755), identifying associations between human leukocyte antigen (HLA) and antibody response for five of eight tested antigens spanning pertussis, diphtheria and hepatitis B vaccines. In addition, through HLA typing 1,702 individuals from 11 populations of African ancestry derived predominantly from the 1000 Genomes Project, we constructed an imputation resource, fine-mapping class II HLA-DR and DQ associations explaining up to 10% of antibody response variance in our infant cohorts. We observed differences in the genetic architecture of pertussis antibody response between the cohorts with African ancestries and an independent cohort with European ancestry, but found no in silico evidence of differences in HLA peptide binding affinity or breadth. Using immune cell expression quantitative trait loci datasets derived from African-ancestry samples from the 1000 Genomes Project, we found evidence of differential HLA-DRB1 expression correlating with inferred protection from pertussis following vaccination. This work suggests that HLA-DRB1 expression may play a role in vaccine response and should be considered alongside peptide selection to improve vaccine design.

Indexed as

HLA-DRB1 ChainsAfrican PeopleAntibody FormationBlack PeopleBurkina FasoEuropean PeopleFemaleHepatitis B VaccinesHumansInfantMalePertussis VaccineQuantitative Trait LociSouth AfricaUgandaVaccinationHepatitis B VaccinesHLA-DRB1 ChainsPertussis Vaccine

Identifiers

PMID38740997
PMCPMC11108778

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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.