Cross-reactive seasonal coronavirus antibody responses contribute to antibody-mediated effector functions against SARS-CoV-2 in individuals in Kenya

Much of sub-Saharan Africa has fared the SARS-CoV-2 pandemic with reduced disease and death even with low uptake of vaccines, little to no infection mitigation strategies, and clear serologic evidence of infection. While warmer weather, a youthful population, and microbiome have been posited to expl...

Full description

Saved in:
Bibliographic Details
Published inThe Journal of immunology (1950) Vol. 210; no. 1_Supplement; pp. 75 - 75.07
Main Authors Ulusan, Sinem, Bai, Shuangyi, Murrell, Amelie, Osoro, Eric, Dawa, Jeanette, Ngere, Isaac, Langat, Robert, Robinson, James, Norton, Elizabeth, Njenga, M. Kariuki, Gunn, Bronwyn
Format Journal Article
LanguageEnglish
Published 01.05.2023
Online AccessGet full text

Cover

Loading…
More Information
Summary:Much of sub-Saharan Africa has fared the SARS-CoV-2 pandemic with reduced disease and death even with low uptake of vaccines, little to no infection mitigation strategies, and clear serologic evidence of infection. While warmer weather, a youthful population, and microbiome have been posited to explain the differences in Africa compared to Americas, we aimed to determine if there was a unique humoral immune response to SARS-CoV-2. To do this, we analyzed SARS-CoV-2 seropositive and seronegative samples from Nairobi, Kenya and compared to a cohort collected in the US in late 2020. We measured the levels of antibodies (Abs) against SARS-CoV-2 Spike [S], receptor binding domain [RBD], and nucleocapsid [N] and hCoVs (229E, NL63, OC43, HKU1) S using a multiplexed Luminex-based assay, and we measured induction of antiviral Ab functions including Ab-dependent cellular phagocytosis (ADCP), neutrophil phagocytosis (ADNP), neutralization, NK cell activation (ADNKA), and complement deposition (ADCD). Correlation network analysis revealed that Ab effector functions were strongly associated with SARS-CoV-2 S, RBD and N-specific Abs in both Kenyan- and US-based cohorts. Surprisingly, we observed that hCoV-specific Abs were correlated with the effector functions against SARS-CoV-2 in the Kenyan samples, but not in the US samples. A subset of Kenyan seronegative subjects displayed ADCP and ADNP against SARS-CoV-2, which was reduced when HKU1-specific IgG was depleted from samples, suggesting cross-reactive Ab responses from hCoVs may augment SARS-CoV-2 immunity. Thus, together these data suggests that unique Ab-mediated functions induced by hCoVs in Africa may help explain the disparity in COVID-19 severity observed across the globe.
ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.210.Supp.75.07