{"title":"Seroprevalence and persistence of humoral immunity in response to SARS-CoV-2 vaccination and mild infection in Morocco: a cross-sectional study.","authors":"Nouhaila Najimi, Chaimae Kadi, Zainab Gaouzi, Nadia Dakka, Rabii Ameziane El Hassani, Fouad Seghrouchni, Youssef Bakri","doi":"10.11604/pamj.2025.51.53.46802","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>assessing the seroprevalence and persistence of humoral immunity through population-based serological surveys is crucial for predicting reinfection risk and optimizing vaccination strategies. In Morocco, a mass vaccination campaign against SARS-CoV-2 has been launched to achieve herd immunity and reduce virus transmission. This study evaluated the humoral immune response to the BBIBP-CorV and ChAdOx1 nCoV-19 vaccines in healthy donors with varying doses and infection histories.</p><p><strong>Methods: </strong>IgG levels were measured via Vircell COVID-19 ELISA, and NAb levels were assessed via the GenScript Surrogate Virus Neutralization Test (sVNT). The study included individuals with different vaccination doses and prior infection histories.</p><p><strong>Results: </strong>the third vaccine dose produced the highest IgG titers, while nonvaccinated individuals and those receiving two doses had lower levels. Prior SARS-CoV-2 infection led to increased antibody levels, suggesting that hybrid immunity offers prolonged protection. The highest NAb titers were observed in individuals receiving three doses, with 96% of previously noninfected individuals being positive for NAb. Risk factor analysis indicated that prior infection (OR = 8.64, 95% CI: 2.52-29.6, p < 0.001) and three doses (OR = 22.1, 95% CI: 2.74-178, p < 0.001) increased immunity.</p><p><strong>Conclusion: </strong>hybrid immunity, involving prior infection and full vaccination, offers enhanced and longer-lasting protection. These results support the need for targeted vaccination strategies to optimize immunity and reduce the risk of adverse outcomes, especially in high-risk populations.</p>","PeriodicalId":48190,"journal":{"name":"Pan African Medical Journal","volume":"51 ","pages":"53"},"PeriodicalIF":1.0000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12433016/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pan African Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11604/pamj.2025.51.53.46802","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: assessing the seroprevalence and persistence of humoral immunity through population-based serological surveys is crucial for predicting reinfection risk and optimizing vaccination strategies. In Morocco, a mass vaccination campaign against SARS-CoV-2 has been launched to achieve herd immunity and reduce virus transmission. This study evaluated the humoral immune response to the BBIBP-CorV and ChAdOx1 nCoV-19 vaccines in healthy donors with varying doses and infection histories.
Methods: IgG levels were measured via Vircell COVID-19 ELISA, and NAb levels were assessed via the GenScript Surrogate Virus Neutralization Test (sVNT). The study included individuals with different vaccination doses and prior infection histories.
Results: the third vaccine dose produced the highest IgG titers, while nonvaccinated individuals and those receiving two doses had lower levels. Prior SARS-CoV-2 infection led to increased antibody levels, suggesting that hybrid immunity offers prolonged protection. The highest NAb titers were observed in individuals receiving three doses, with 96% of previously noninfected individuals being positive for NAb. Risk factor analysis indicated that prior infection (OR = 8.64, 95% CI: 2.52-29.6, p < 0.001) and three doses (OR = 22.1, 95% CI: 2.74-178, p < 0.001) increased immunity.
Conclusion: hybrid immunity, involving prior infection and full vaccination, offers enhanced and longer-lasting protection. These results support the need for targeted vaccination strategies to optimize immunity and reduce the risk of adverse outcomes, especially in high-risk populations.