Sustained spike-specific IgG antibodies following CoronaVac (Sinovac) vaccination in sub-Saharan Africa, but increased breakthrough infections in baseline spike-naive individuals.
COVID-19
CoronaVac
antibody concentrations
antibody persistence
breakthrough infections
seropositivity
spike protein
sub-Saharan Africa
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2023
2023
Historique:
received:
09
07
2023
accepted:
14
11
2023
medline:
17
12
2023
pubmed:
15
12
2023
entrez:
15
12
2023
Statut:
epublish
Résumé
This study investigated the antibody responses to the inactivated COVID-19 vaccine, CoronaVac (Sinovac Biotech) in the African population to provide valuable insights into long-term immunity and breakthrough infections against SARS-CoV-2 in individuals with varying prior IgG seropositivity. Real-life cohorts were used to longitudinally track antibody levels against the SARS-CoV-2 spike and nucleoprotein in 60 participants over 12 months to examine the levels of multiple antibody isotypes (S-IgG, S-IgM, S-IgA, N-IgG, and N-IgM). Throughout the 12 months, we observed consistently high and stable seropositivity rates for spike-IgG antibodies, spike-IgM antibodies showed a decline in frequencies over time, and spike-IgA levels remained moderate and stable. Vaccinated individuals previously positive for spike-IgG antibodies demonstrated strong and persistent seropositivity, while those initially negative experienced a gradual and delayed increase in seropositivity rates. The fold change analysis of S- and N- antibody responses demonstrated a consistently stable and comparable profile over time, indicating that vaccine-induced antibody responses remain constant and lack significant fluctuations beyond the initial boost. The study emphasized that individuals lacking previous IgG positivity showed reduced vaccine-induced spike-IgG antibodies and were more susceptible to breakthrough infections, highlighting their higher vulnerability. All cases of breakthrough infections were asymptomatic, indicating the conferred protection to the vaccinated individuals. The findings corroborated earlier studies on the effectiveness of the CoronaVac vaccine and emphasized the significance of accounting for pre-existing seropositivity in vaccine assessments. This study effectively demonstrated durable antibody responses against SARS-CoV-2 in the African population following the CoronaVac vaccination, providing crucial insights for informing vaccination strategies and safeguarding vulnerable populations. Continuous surveillance is imperative for tracking breakthrough infections and monitoring waning immunity. The insights gained offer crucial direction for public health strategies and enhance comprehension of vaccine effectiveness in sub-Saharan Africa. Further research should explore functional outcomes, cellular immune responses, and the vaccine's effectiveness against different variants to enhance our understanding and optimize vaccine strategies.
Identifiants
pubmed: 38098482
doi: 10.3389/fimmu.2023.1255676
pmc: PMC10720323
doi:
Substances chimiques
sinovac COVID-19 vaccine
0
COVID-19 Vaccines
0
Immunoglobulin G
0
Immunoglobulin M
0
Blood Group Antigens
0
Immunoglobulin A
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1255676Subventions
Organisme : NIAID NIH HHS
ID : HHSN272201400008C
Pays : United States
Organisme : Bill & Melinda Gates Foundation
ID : INV-036306
Pays : United States
Organisme : Medical Research Council
ID : MC_UU_00027/5
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00033/1
Pays : United Kingdom
Informations de copyright
Copyright © 2023 Sembera, Baine, Ankunda, Katende, Oluka, Akoli, Kato, Odoch, Ejou, Opio, Musenero, 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
Viruses. 2021 Nov 23;13(12):
pubmed: 34960605
Sci Rep. 2022 Jul 14;12(1):12038
pubmed: 35835822
Can J Microbiol. 2022 Aug 1;68(8):543-550
pubmed: 35852365
J Clin Invest. 2014 Jul;124(7):3147-58
pubmed: 24911151
Vaccines (Basel). 2023 Feb 03;11(2):
pubmed: 36851233
Hum Vaccin Immunother. 2021 Oct 3;17(10):3310-3313
pubmed: 34348570
Lancet Infect Dis. 2023 Apr;23(4):435-444
pubmed: 36436536
Lancet Microbe. 2022 Mar;3(3):e235-e240
pubmed: 34723229
Microbiol Spectr. 2022 Aug 31;10(4):e0098622
pubmed: 35867423
Rev Panam Salud Publica. 2022 Aug 18;46:e106
pubmed: 36016834
Front Immunol. 2021 Sep 29;12:742914
pubmed: 34659237
Nature. 2021 Dec;600(7889):530-535
pubmed: 34670266
Expert Rev Vaccines. 2021 Aug;20(8):945-957
pubmed: 34224290
Lancet. 2022 Feb 5;399(10324):521-529
pubmed: 35074136
Front Immunol. 2023 Apr 17;14:1156758
pubmed: 37153606
Lancet Infect Dis. 2023 May;23(5):556-567
pubmed: 36681084
Environ Res. 2022 Jun;209:112911
pubmed: 35149106
Front Immunol. 2022 Jan 03;12:809244
pubmed: 35046961
Annu Rev Public Health. 2000;21:15-46
pubmed: 10884944
Lancet. 2021 Mar 20;397(10279):1075-1084
pubmed: 33743869
Viruses. 2023 Apr 04;15(4):
pubmed: 37112897
J Biol Chem. 2021 Jan-Jun;296:100111
pubmed: 33229438
Front Immunol. 2023 Mar 16;14:1152522
pubmed: 37006272
Front Immunol. 2023 May 02;14:1183983
pubmed: 37205095
Front Immunol. 2021 Dec 22;12:802858
pubmed: 35003131
Int J Infect Dis. 2022 Jan;114:252-260
pubmed: 34800687
Lancet Microbe. 2023 Mar;4(3):e149-e158
pubmed: 36716754
Signal Transduct Target Ther. 2023 May 4;8(1):179
pubmed: 37142583
Front Immunol. 2021 Oct 12;12:744887
pubmed: 34712232
Vaccines (Basel). 2023 Feb 23;11(3):
pubmed: 36992107
Rev Soc Bras Med Trop. 2023 Feb 20;56:e0209
pubmed: 36820653
Int Immunopharmacol. 2022 Feb;103:108491
pubmed: 34954559
Clin Microbiol Infect. 2022 Feb;28(2):202-221
pubmed: 34715347
Front Immunol. 2023 Mar 14;14:1113194
pubmed: 36999017