Trends in SARS-CoV-2 seroprevalence among pregnant women attending first antenatal care visits in Zambia: A repeated cross-sectional survey, 2021-2022.


Journal

PLOS global public health
ISSN: 2767-3375
Titre abrégé: PLOS Glob Public Health
Pays: United States
ID NLM: 9918283779606676

Informations de publication

Date de publication:
2024
Historique:
received: 07 12 2023
accepted: 11 03 2024
medline: 3 4 2024
pubmed: 3 4 2024
entrez: 3 4 2024
Statut: epublish

Résumé

SARS-CoV-2 serosurveys help estimate the extent of transmission and guide the allocation of COVID-19 vaccines. We measured SARS-CoV-2 seroprevalence among women attending ANC clinics to assess exposure trends over time in Zambia. We conducted repeated cross-sectional SARS-CoV-2 seroprevalence surveys among pregnant women aged 15-49 years attending their first ANC visits in four districts of Zambia (two urban and two rural) during September 2021-September 2022. Serologic testing was done using a multiplex bead assay which detects IgG antibodies to the nucleocapsid protein and the spike protein receptor-binding domain (RBD). We calculated monthly SARS-CoV-2 seroprevalence by district. We also categorized seropositive results as infection alone, infection and vaccination, or vaccination alone based on anti-RBD and anti-nucleocapsid test results and self-reported COVID-19 vaccination status (vaccinated was having received ≥1 dose). Among 8,304 participants, 5,296 (63.8%) were cumulatively seropositive for SARS-CoV-2 antibodies from September 2021 through September 2022. SARS-CoV-2 seroprevalence primarily increased from September 2021 to September 2022 in three districts (Lusaka: 61.8-100.0%, Chongwe: 39.6-94.7%, Chipata: 56.5-95.0%), but in Chadiza, seroprevalence increased from 27.8% in September 2021 to 77.2% in April 2022 before gradually dropping to 56.6% in July 2022. Among 5,906 participants with a valid COVID-19 vaccination status, infection alone accounted for antibody responses in 77.7% (4,590) of participants. Most women attending ANC had evidence of prior SARS-CoV-2 infection and most SARS-CoV-2 seropositivity was infection-induced. Capturing COVID-19 vaccination status and using a multiplex bead assay with anti-nucleocapsid and anti-RBD targets facilitated distinguishing infection-induced versus vaccine-induced antibody responses during a period of increasing COVID-19 vaccine coverage in Zambia. Declining seroprevalence in Chadiza may indicate waning antibodies and a need for booster vaccines. ANC clinics have a potential role in ongoing SARS-CoV-2 serosurveillance and can continue to provide insights into SARS-CoV-2 antibody dynamics to inform near real-time public health responses.

Identifiants

pubmed: 38568905
doi: 10.1371/journal.pgph.0003073
pii: PGPH-D-23-02441
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0003073

Informations de copyright

Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Elizabeth Heilmann (E)

Public Health Institute, Oakland, California, United States of America.
Division of Global HIV and Tuberculosis, U.S. Centers for Disease Control and Prevention, Lusaka, Zambia.

Tannia Tembo (T)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Sombo Fwoloshi (S)

Division of Infectious Diseases, Ministry of Health, Lusaka, Zambia.

Felix Chilambe (F)

Adult Centre of Excellence, University Teaching Hospital, Lusaka, Zambia.

Kalubi Kalenga (K)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Mpanji Siwingwa (M)

Adult Centre of Excellence, University Teaching Hospital, Lusaka, Zambia.

Conceptor Mulube (C)

PATH, Lusaka, Zambia.

Victoria Seffren (V)

Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Carolyn Bolton-Moore (C)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

John Simwanza (J)

Surveillance and Disease Intelligence, Zambia National Public Health Institute, Lusaka, Zambia.

Samuel Yingst (S)

Division of Global HIV and Tuberculosis, U.S. Centers for Disease Control and Prevention, Lusaka, Zambia.

Ruchi Yadav (R)

Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Eric Rogier (E)

Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Andrew F Auld (AF)

Division of Global HIV and Tuberculosis, U.S. Centers for Disease Control and Prevention, Lusaka, Zambia.

Simon Agolory (S)

Division of Global HIV and Tuberculosis, U.S. Centers for Disease Control and Prevention, Lusaka, Zambia.

Muzala Kapina (M)

Surveillance and Disease Intelligence, Zambia National Public Health Institute, Lusaka, Zambia.

Julie R Gutman (JR)

Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Theodora Savory (T)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Chabu Kangale (C)

PATH, Lusaka, Zambia.

Lloyd B Mulenga (LB)

Division of Infectious Diseases, Ministry of Health, Lusaka, Zambia.

Izukanji Sikazwe (I)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Jonas Z Hines (JZ)

Division of Global HIV and Tuberculosis, U.S. Centers for Disease Control and Prevention, Lusaka, Zambia.

Classifications MeSH