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Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi

BACKGROUND: The B.1.1.529 (Omicron) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in the fourth COVID-19 pandemic wave across the southern African region, including Malawi. The seroprevalence of SARS-CoV-2 antibodies and their association with epidemiological t...

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Autores principales: Mseka, Upendo L., Mandolo, Jonathan, Nyoni, Kenneth, Divala, Oscar, Kambalame, Dzinkambani, Mapemba, Daniel, Kamzati, Moses, Chibwe, Innocent, Henrion, Marc Y.R., Manda, Kingsley, Thindwa, Deus, Mvula, Memory, Odala, Bright, Kamng'ona, Raphael, Dzinza, Nelson, Jere, Khuzwayo C., Feasey, Nicholas, Ho, Antonia, Amoah, Abena S., Gordon, Melita, Swarthout, Todd D., Crampin, Amelia, Heyderman, Robert S., Kagoli, Matthew, Chitsa-Banda, Evelyn, Mitambo, Collins, Phuka, John, Chilima, Benson, Kasambara, Watipaso, Jambo, Kondwani C., Chauma-Mwale, Annie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800171/
https://www.ncbi.nlm.nih.gov/pubmed/36600885
http://dx.doi.org/10.1016/j.eclinm.2022.101800
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author Mseka, Upendo L.
Mandolo, Jonathan
Nyoni, Kenneth
Divala, Oscar
Kambalame, Dzinkambani
Mapemba, Daniel
Kamzati, Moses
Chibwe, Innocent
Henrion, Marc Y.R.
Manda, Kingsley
Thindwa, Deus
Mvula, Memory
Odala, Bright
Kamng'ona, Raphael
Dzinza, Nelson
Jere, Khuzwayo C.
Feasey, Nicholas
Ho, Antonia
Amoah, Abena S.
Gordon, Melita
Swarthout, Todd D.
Crampin, Amelia
Heyderman, Robert S.
Kagoli, Matthew
Chitsa-Banda, Evelyn
Mitambo, Collins
Phuka, John
Chilima, Benson
Kasambara, Watipaso
Jambo, Kondwani C.
Chauma-Mwale, Annie
author_facet Mseka, Upendo L.
Mandolo, Jonathan
Nyoni, Kenneth
Divala, Oscar
Kambalame, Dzinkambani
Mapemba, Daniel
Kamzati, Moses
Chibwe, Innocent
Henrion, Marc Y.R.
Manda, Kingsley
Thindwa, Deus
Mvula, Memory
Odala, Bright
Kamng'ona, Raphael
Dzinza, Nelson
Jere, Khuzwayo C.
Feasey, Nicholas
Ho, Antonia
Amoah, Abena S.
Gordon, Melita
Swarthout, Todd D.
Crampin, Amelia
Heyderman, Robert S.
Kagoli, Matthew
Chitsa-Banda, Evelyn
Mitambo, Collins
Phuka, John
Chilima, Benson
Kasambara, Watipaso
Jambo, Kondwani C.
Chauma-Mwale, Annie
author_sort Mseka, Upendo L.
collection PubMed
description BACKGROUND: The B.1.1.529 (Omicron) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in the fourth COVID-19 pandemic wave across the southern African region, including Malawi. The seroprevalence of SARS-CoV-2 antibodies and their association with epidemiological trends of hospitalisations and deaths are needed to aid locally relevant public health policy decisions. METHODS: We conducted a population-based serosurvey from December 27, 2021 to January 17, 2022, in 7 districts across Malawi to determine the seroprevalence of SARS-CoV-2 antibodies. Serum samples were tested for antibodies against SARS-CoV-2 receptor binding domain using WANTAI SARS-CoV-2 Receptor Binding Domain total antibody commercial enzyme-linked immunosorbent assay (ELISA). We also evaluated COVID-19 epidemiologic trends in Malawi, including cases, hospitalisations and deaths from April 1, 2021 through April 30, 2022, collected using the routine national COVID-19 reporting system. A multivariable logistic regression model was developed to investigate the factors associated with SARS-CoV-2 seropositivity. FINDINGS: Serum samples were analysed from 4619 participants (57% female; 60% aged 18–50 years), of whom 878/3794 (23%) of vaccine eligible adults had received a single dose of any COVID-19 vaccine. The overall assay-adjusted seroprevalence was 83.7% (95% confidence interval (CI), 79.3%–93.4%). Seroprevalence was lowest among children <13 years of age (66%) and highest among adults 18–50 years of age (82%). Seroprevalence was higher among vaccinated compared to unvaccinated participants (1 dose, 94% vs. 77%, adjusted odds ratio 4.89 [95% CI, 3.43–7.22]; 2 doses, 97% vs. 77%, aOR 6.62 [95% CI, 4.14–11.3]). Urban residents were more likely to be seropositive than those from rural settings (91% vs. 78%, aOR 2.76 [95% CI, 2.16–3.55]). There was at least a two-fold reduction in the proportion of hospitalisations and deaths among the reported cases in the fourth wave compared to the third wave (hospitalisations, 10.7% (95% CI, 10.2–11.3) vs. 4.86% (95% CI, 4.52–5.23), p < 0.0001; deaths, 3.48% (95% CI, 3.18–3.81) vs. 1.15% (95% CI, 1.00–1.34), p < 0.0001). INTERPRETATION: We report reduction in proportion of hospitalisations and deaths from SARS-CoV-2 infections during the Omicron variant dominated wave in Malawi, in the context of high SARS-CoV-2 seroprevalence and low COVID-19 vaccination coverage. These findings suggest that COVID-19 vaccination policy in high seroprevalence settings may need to be amended from mass campaigns to targeted vaccination of reported at-risk populations. FUNDING: Supported by the 10.13039/100000865Bill and Melinda Gates Foundation (INV-039481).
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spelling pubmed-98001712022-12-30 Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi Mseka, Upendo L. Mandolo, Jonathan Nyoni, Kenneth Divala, Oscar Kambalame, Dzinkambani Mapemba, Daniel Kamzati, Moses Chibwe, Innocent Henrion, Marc Y.R. Manda, Kingsley Thindwa, Deus Mvula, Memory Odala, Bright Kamng'ona, Raphael Dzinza, Nelson Jere, Khuzwayo C. Feasey, Nicholas Ho, Antonia Amoah, Abena S. Gordon, Melita Swarthout, Todd D. Crampin, Amelia Heyderman, Robert S. Kagoli, Matthew Chitsa-Banda, Evelyn Mitambo, Collins Phuka, John Chilima, Benson Kasambara, Watipaso Jambo, Kondwani C. Chauma-Mwale, Annie eClinicalMedicine Articles BACKGROUND: The B.1.1.529 (Omicron) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in the fourth COVID-19 pandemic wave across the southern African region, including Malawi. The seroprevalence of SARS-CoV-2 antibodies and their association with epidemiological trends of hospitalisations and deaths are needed to aid locally relevant public health policy decisions. METHODS: We conducted a population-based serosurvey from December 27, 2021 to January 17, 2022, in 7 districts across Malawi to determine the seroprevalence of SARS-CoV-2 antibodies. Serum samples were tested for antibodies against SARS-CoV-2 receptor binding domain using WANTAI SARS-CoV-2 Receptor Binding Domain total antibody commercial enzyme-linked immunosorbent assay (ELISA). We also evaluated COVID-19 epidemiologic trends in Malawi, including cases, hospitalisations and deaths from April 1, 2021 through April 30, 2022, collected using the routine national COVID-19 reporting system. A multivariable logistic regression model was developed to investigate the factors associated with SARS-CoV-2 seropositivity. FINDINGS: Serum samples were analysed from 4619 participants (57% female; 60% aged 18–50 years), of whom 878/3794 (23%) of vaccine eligible adults had received a single dose of any COVID-19 vaccine. The overall assay-adjusted seroprevalence was 83.7% (95% confidence interval (CI), 79.3%–93.4%). Seroprevalence was lowest among children <13 years of age (66%) and highest among adults 18–50 years of age (82%). Seroprevalence was higher among vaccinated compared to unvaccinated participants (1 dose, 94% vs. 77%, adjusted odds ratio 4.89 [95% CI, 3.43–7.22]; 2 doses, 97% vs. 77%, aOR 6.62 [95% CI, 4.14–11.3]). Urban residents were more likely to be seropositive than those from rural settings (91% vs. 78%, aOR 2.76 [95% CI, 2.16–3.55]). There was at least a two-fold reduction in the proportion of hospitalisations and deaths among the reported cases in the fourth wave compared to the third wave (hospitalisations, 10.7% (95% CI, 10.2–11.3) vs. 4.86% (95% CI, 4.52–5.23), p < 0.0001; deaths, 3.48% (95% CI, 3.18–3.81) vs. 1.15% (95% CI, 1.00–1.34), p < 0.0001). INTERPRETATION: We report reduction in proportion of hospitalisations and deaths from SARS-CoV-2 infections during the Omicron variant dominated wave in Malawi, in the context of high SARS-CoV-2 seroprevalence and low COVID-19 vaccination coverage. These findings suggest that COVID-19 vaccination policy in high seroprevalence settings may need to be amended from mass campaigns to targeted vaccination of reported at-risk populations. FUNDING: Supported by the 10.13039/100000865Bill and Melinda Gates Foundation (INV-039481). Elsevier 2022-12-30 /pmc/articles/PMC9800171/ /pubmed/36600885 http://dx.doi.org/10.1016/j.eclinm.2022.101800 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Mseka, Upendo L.
Mandolo, Jonathan
Nyoni, Kenneth
Divala, Oscar
Kambalame, Dzinkambani
Mapemba, Daniel
Kamzati, Moses
Chibwe, Innocent
Henrion, Marc Y.R.
Manda, Kingsley
Thindwa, Deus
Mvula, Memory
Odala, Bright
Kamng'ona, Raphael
Dzinza, Nelson
Jere, Khuzwayo C.
Feasey, Nicholas
Ho, Antonia
Amoah, Abena S.
Gordon, Melita
Swarthout, Todd D.
Crampin, Amelia
Heyderman, Robert S.
Kagoli, Matthew
Chitsa-Banda, Evelyn
Mitambo, Collins
Phuka, John
Chilima, Benson
Kasambara, Watipaso
Jambo, Kondwani C.
Chauma-Mwale, Annie
Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title_full Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title_fullStr Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title_full_unstemmed Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title_short Omicron B.1.1.529 variant infections associated with severe disease are uncommon in a COVID-19 under-vaccinated, high SARS-CoV-2 seroprevalence population in Malawi
title_sort omicron b.1.1.529 variant infections associated with severe disease are uncommon in a covid-19 under-vaccinated, high sars-cov-2 seroprevalence population in malawi
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800171/
https://www.ncbi.nlm.nih.gov/pubmed/36600885
http://dx.doi.org/10.1016/j.eclinm.2022.101800
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