The subdued post-boost spike-directed secondary IgG antibody response in Ugandan recipients of the Pfizer-BioNTech BNT162b2 vaccine has implications for local vaccination policies.

IgG IgM and IgA antibodies Pfizer BioNTech BNT162b2 COVID-19 vaccine Sub-Saharan African populations Ugandan population booster dose breakthrough infections longitudinal antibody responses seropositivity classification

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 21 10 2023
accepted: 31 01 2024
medline: 13 3 2024
pubmed: 12 3 2024
entrez: 12 3 2024
Statut: epublish

Résumé

This study aimed to delineate longitudinal antibody responses to the Pfizer-BioNTech BNT162b2 COVID-19 vaccine within the Ugandan subset of the Sub-Saharan African (SSA) demographic, filling a significant gap in global datasets. We enrolled 48 participants and collected 320 specimens over 12 months after the primary vaccination dose. A validated enzyme-linked immunosorbent assay (ELISA) was used to quantify SARS-CoV-2-specific IgG, IgM, and IgA antibody concentrations (ng/ml) and optical densities (ODs). Statistical analyses included box plots, diverging bar graphs, and the Wilcoxon test with Bonferroni correction. We noted a robust S-IgG response within 14 days of the primary vaccine dose, which was consistent with global data. There was no significant surge in S-IgG levels after the booster dose, contrasting trends in other global populations. The S-IgM response was transient and predominantly below established thresholds for this population, which reflects its typical early emergence and rapid decline. S-IgA levels rose after the initial dose then decreased after six months, aligning with the temporal patterns of mucosal immunity. Eleven breakthrough infections were noted, and all were asymptomatic, regardless of the participants' initial S-IgG serostatus, which suggests a protective effect from vaccination. The Pfizer-BioNTech BNT162b2 COVID-19 vaccine elicited strong S-IgG responses in the SSA demographic. The antibody dynamics distinctly differed from global data highlighting the significance of region-specific research and the necessity for customised vaccination strategies.

Identifiants

pubmed: 38469296
doi: 10.3389/fimmu.2024.1325387
pmc: PMC10926532
doi:

Substances chimiques

Immunoglobulin G 0
BNT162 Vaccine 0
COVID-19 Vaccines 0
Vaccines 0
Antibodies, Viral 0
Immunoglobulin M 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1325387

Subventions

Organisme : Medical Research Council
ID : MC_UU_00033/1
Pays : United Kingdom

Investigateurs

Christine Hermilia Akoli (CH)
Angela Namuyanja (A)
Solomon Opio (S)
Arthur Watelo Kalyebi (AW)
Ivan Ssali (I)
Ben Gombe (B)
Susan Mugaba (S)
Hellen Nantambi (H)

Informations de copyright

Copyright © 2024 Ankunda, Katende, Oluka, Sembera, Baine, Odoch, Ejou, Kato, and The COVID-19 Immunoprofiling Team, Kaleebu and Serwanga.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Microbiol Spectr. 2022 Dec 21;10(6):e0271622
pubmed: 36219096
J Infect Dis. 2023 Nov 11;228(10):1311-1313
pubmed: 37592872
PLoS One. 2023 Jul 12;18(7):e0288557
pubmed: 37437051
J Med Virol. 2022 Jul;94(7):2939-2961
pubmed: 35229324
J Clin Invest. 2014 Jul;124(7):3147-58
pubmed: 24911151
Front Immunol. 2018 Oct 09;9:2295
pubmed: 30356757
Immunogenetics. 2023 Jun;75(3):207-214
pubmed: 37084013
Immunobiology. 2023 Sep;228(5):152720
pubmed: 37541134
Nat Med. 2022 May;28(5):1042-1049
pubmed: 35241844
Front Cell Infect Microbiol. 2021 Apr 06;11:655896
pubmed: 33889552
Microbiol Spectr. 2022 Apr 27;10(2):e0181421
pubmed: 35293796
Clin Microbiol Rev. 2019 Mar 13;32(2):
pubmed: 30867162
Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2277-81
pubmed: 1347946
J Clin Immunol. 2023 Nov;43(8):1724-1739
pubmed: 37606852
Lancet. 2021 Mar 20;397(10279):1057-1058
pubmed: 33640038
Hum Genet. 2008 Jul;123(6):557-98
pubmed: 18512079
Clin Infect Dis. 2023 Feb 8;76(3):e439-e449
pubmed: 35608504
Vaccines (Basel). 2023 Dec 10;11(12):
pubmed: 38140239
Sci Transl Med. 2021 Jan 20;13(577):
pubmed: 33288662
EBioMedicine. 2022 Jan;75:103805
pubmed: 35032961
Front Immunol. 2022 Nov 08;13:948335
pubmed: 36426367
mBio. 2022 Jan 25;13(1):e0214121
pubmed: 35073738
PLoS Negl Trop Dis. 2023 Jul 5;17(7):e0011089
pubmed: 37406029
Nature. 2020 Oct;586(7830):589-593
pubmed: 32785213
EClinicalMedicine. 2023 Apr;58:101926
pubmed: 37034357
Front Immunol. 2023 Nov 30;14:1255676
pubmed: 38098482
HLA. 2023 Aug;102(2):192-205
pubmed: 36999238
Immunogenetics. 2023 Jun;75(3):309-320
pubmed: 36534127
J Virol. 2019 Aug 28;93(18):
pubmed: 31243126
Parasitol Int. 2020 Oct;78:102132
pubmed: 32387542
Front Immunol. 2023 Mar 16;14:1152522
pubmed: 37006272
Bio Protoc. 2023 Dec 20;13(24):e4905
pubmed: 38156036
Front Immunol. 2023 May 02;14:1183983
pubmed: 37205095
Malar J. 2021 Feb 25;20(1):111
pubmed: 33632228
Eur J Med Res. 2023 Aug 27;28(1):299
pubmed: 37635240
Nat Commun. 2022 Oct 17;13(1):6131
pubmed: 36253377
Viruses. 2023 Mar 31;15(4):
pubmed: 37112884
Int Immunopharmacol. 2022 Feb;103:108491
pubmed: 34954559
Front Immunol. 2023 Mar 14;14:1113194
pubmed: 36999017
N Engl J Med. 2020 Dec 31;383(27):2603-2615
pubmed: 33301246
Front Immunol. 2023 Apr 19;14:1148877
pubmed: 37153598
N Engl J Med. 2020 Dec 17;383(25):2439-2450
pubmed: 33053279

Auteurs

Violet Ankunda (V)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.

Joseph Ssebwana Katende (JS)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.
Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Gerald Kevin Oluka (GK)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.
Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Jackson Sembera (J)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.

Claire Baine (C)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.

Geoffrey Odoch (G)

Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Peter Ejou (P)

Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Laban Kato (L)

Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Pontiano Kaleebu (P)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.
Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Jennifer Serwanga (J)

Viral Pathogens Research Theme, Medical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine, Uganda Research Unit, Entebbe, Uganda.
Department of Immunology, Uganda Virus Research Institute, Entebbe, Uganda.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH