Evaluation of population immunity against SARS-CoV-2 variants, EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1 using samples from two health demographic surveillance systems in Kenya

Increased immune evasion by emerging and highly mutated SARS-CoV-2 variants is a key challenge to the control of COVID-19. The majority of these mutations mainly target the spike protein, allowing the new variants to escape the immunity previously raised by vaccination and/or infection by earlier variants of SARS-CoV-2. In this study, we investigated the neutralizing capacity of antibodies against emerging variants of interest circulating between May 2023 and October 2024 using sera from representative samples of the Kenyan population. From our genomics data, we identified the most prevalent Kenyan and global variants and performed pseudoviruses neutralization assays with the most recent SARS-CoV-2 variants. Our data show that antibodies from individuals in the general population in Kenya were less effective against the recent prevalent SARS-CoV-2 omicron variants (i.e. EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1) compared to the ancestral wildtype strain. Although there was increased neutralization following multiple doses of vaccine, antibodies from > 40% of the vaccinated individuals did not neutralize the omicron variants, suggesting that individuals were susceptible to infection by these variants.

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Publication Details

Journal
BMC Infectious Diseases
Published
2024-12-28
DOI
https://doi.org/10.1186/s12879-024-10367-3
Citations
10
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
3.89

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article

Evaluation of population immunity against SARS-CoV-2 variants, EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1 using samples from two health demographic surveillance systems in Kenya

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10 citations
BMC Infectious Diseases
SARS-CoV-2 and COVID-19 Research
3.89
article

Evaluation of population immunity against SARS-CoV-2 variants, EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1 using samples from two health demographic surveillance systems in Kenya

Charles Sande, J. Anthony G. Scott, Makobu Kimani, Charles N. Agoti, Angela Karani, George Githinji, Boniface Karia, Lynette Isabella Ochola‐Oyier, Dalan Bailey, Daisy Mugo, Arnold W. Lambisia, Abdhalah Ziraba, Bernadette Kutima, Ruth Lucinde, Eunice Wambui Nduati, John N. Gitonga, Antipa Sigilai, Joseph Newman, Donald Akech, James Nyagwange, Donwilliams O. Omuoyo, George M. Warimwe, Ambrose Agweyu, Doreen Lugano, Sharon Owuor, Angela Maina, Philip Bejon, Wangeci Kagucia, Gloria Konyino
article en
10 citations

Abstract

Increased immune evasion by emerging and highly mutated SARS-CoV-2 variants is a key challenge to the control of COVID-19. The majority of these mutations mainly target the spike protein, allowing the new variants to escape the immunity previously raised by vaccination and/or infection by earlier variants of SARS-CoV-2. In this study, we investigated the neutralizing capacity of antibodies against emerging variants of interest circulating between May 2023 and October 2024 using sera from representative samples of the Kenyan population. From our genomics data, we identified the most prevalent Kenyan and global variants and performed pseudoviruses neutralization assays with the most recent SARS-CoV-2 variants. Our data show that antibodies from individuals in the general population in Kenya were less effective against the recent prevalent SARS-CoV-2 omicron variants (i.e. EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1) compared to the ancestral wildtype strain. Although there was increased neutralization following multiple doses of vaccine, antibodies from > 40% of the vaccinated individuals did not neutralize the omicron variants, suggesting that individuals were susceptible to infection by these variants.

BMC Infectious DiseasesVol. 24(1)
University of London (GB), The Pirbright Institute (GB), Kenya Medical Research Institute (KE), University of Oxford (GB), London School of Hygiene & Tropical Medicine (GB), African Population and Health Research Center (KE), Wellcome Trust (GB)
Bill and Melinda Gates Foundation, Wellcome Trust, Medical Research Council, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 5%
SARS-CoV-2 and COVID-19 Research
3.89
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