SARS-CoV-2 seroprevalence, cumulative infections, and immunity to symptomatic infection – A multistage national household survey and modelling study, Dominican Republic, June–October 2021
Population-level SARS-CoV-2 immunological protection is poorly understood but can guide vaccination and non-pharmaceutical intervention priorities. Our objective was to characterise cumulative infections and immunological protection in the Dominican Republic. Household members ≥5 years were enrolled...
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Veröffentlicht in: | Lancet Regional Health - Americas (Online) 2022-12, Vol.16, p.100390-100390, Article 100390 |
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creator | Nilles, Eric J. Paulino, Cecilia Then de St. Aubin, Michael Restrepo, Angela Cadavid Mayfield, Helen Dumas, Devan Finch, Emilie Garnier, Salome Etienne, Marie Caroline Iselin, Louisa Duke, William Jarolim, Petr Oasan, Timothy Yu, Jingyou Wan, Huahua Peña, Farah Iihoshi, Naomi Abdalla, Gabriela Lopez, Beatriz Cruz, Lucia de la Henríquez, Bernarda Espinosa-Bode, Andres Puello, Yosanly Cornelio Durski, Kara Baldwin, Margaret Baez, Amado Alejandro Merchant, Roland C. Barouch, Dan H. Skewes-Ramm, Ronald Gutiérrez, Emily Zielinski Kucharski, Adam Lau, Colleen L. |
description | Population-level SARS-CoV-2 immunological protection is poorly understood but can guide vaccination and non-pharmaceutical intervention priorities. Our objective was to characterise cumulative infections and immunological protection in the Dominican Republic.
Household members ≥5 years were enrolled in a three-stage national household cluster serosurvey in the Dominican Republic. We measured pan-immunoglobulin antibodies against the SARS-CoV-2 spike (anti-S) and nucleocapsid glycoproteins, and pseudovirus neutralising activity against the ancestral and B.1.617.2 (Delta) strains. Seroprevalence and cumulative prior infections were weighted and adjusted for assay performance and seroreversion. Binary classification machine learning methods and pseudovirus neutralising correlates of protection were used to estimate 50% and 80% protection against symptomatic infection.
Between 30 Jun and 12 Oct 2021 we enrolled 6683 individuals from 3832 households. We estimate that 85.0% (CI 82.1–88.0) of the ≥5 years population had been immunologically exposed and 77.5% (CI 71.3–83) had been previously infected. Protective immunity sufficient to provide at least 50% protection against symptomatic SARS-CoV-2 infection was estimated in 78.1% (CI 74.3–82) and 66.3% (CI 62.8–70) of the population for the ancestral and Delta strains respectively. Younger (5–14 years, OR 0.47 [CI 0.36–0.61]) and older (≥75-years, 0.40 [CI 0.28–0.56]) age, working outdoors (0.53 [0.39–0.73]), smoking (0.66 [0.52–0.84]), urban setting (1.30 [1.14–1.49]), and three vs no vaccine doses (18.41 [10.69–35.04]) were associated with 50% protection against the ancestral strain.
Cumulative infections substantially exceeded prior estimates and overall immunological exposure was high. After controlling for confounders, markedly lower immunological protection was observed to the ancestral and Delta strains across certain subgroups, findings that can guide public health interventions and may be generalisable to other settings and viral strains.
This study was funded by the US CDC. |
doi_str_mv | 10.1016/j.lana.2022.100390 |
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Household members ≥5 years were enrolled in a three-stage national household cluster serosurvey in the Dominican Republic. We measured pan-immunoglobulin antibodies against the SARS-CoV-2 spike (anti-S) and nucleocapsid glycoproteins, and pseudovirus neutralising activity against the ancestral and B.1.617.2 (Delta) strains. Seroprevalence and cumulative prior infections were weighted and adjusted for assay performance and seroreversion. Binary classification machine learning methods and pseudovirus neutralising correlates of protection were used to estimate 50% and 80% protection against symptomatic infection.
Between 30 Jun and 12 Oct 2021 we enrolled 6683 individuals from 3832 households. We estimate that 85.0% (CI 82.1–88.0) of the ≥5 years population had been immunologically exposed and 77.5% (CI 71.3–83) had been previously infected. Protective immunity sufficient to provide at least 50% protection against symptomatic SARS-CoV-2 infection was estimated in 78.1% (CI 74.3–82) and 66.3% (CI 62.8–70) of the population for the ancestral and Delta strains respectively. Younger (5–14 years, OR 0.47 [CI 0.36–0.61]) and older (≥75-years, 0.40 [CI 0.28–0.56]) age, working outdoors (0.53 [0.39–0.73]), smoking (0.66 [0.52–0.84]), urban setting (1.30 [1.14–1.49]), and three vs no vaccine doses (18.41 [10.69–35.04]) were associated with 50% protection against the ancestral strain.
Cumulative infections substantially exceeded prior estimates and overall immunological exposure was high. After controlling for confounders, markedly lower immunological protection was observed to the ancestral and Delta strains across certain subgroups, findings that can guide public health interventions and may be generalisable to other settings and viral strains.
This study was funded by the US CDC.</description><identifier>ISSN: 2667-193X</identifier><identifier>EISSN: 2667-193X</identifier><identifier>DOI: 10.1016/j.lana.2022.100390</identifier><identifier>PMID: 36408529</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><ispartof>Lancet Regional Health - Americas (Online), 2022-12, Vol.16, p.100390-100390, Article 100390</ispartof><rights>2022 The Author(s)</rights><rights>2022 The Author(s).</rights><rights>2022 The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-d9a18b9da3787d26b11667bfa69328a68fcb8ff748c8d430e9648e8ae3ec615a3</citedby><cites>FETCH-LOGICAL-c455t-d9a18b9da3787d26b11667bfa69328a68fcb8ff748c8d430e9648e8ae3ec615a3</cites><orcidid>0000-0002-3594-4330 ; 0000-0002-8399-9205 ; 0000-0001-7308-6552 ; 0000-0002-2355-3586 ; 0000-0001-7044-5257 ; 0000-0003-1353-9948</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642112/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642112/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36408529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nilles, Eric J.</creatorcontrib><creatorcontrib>Paulino, Cecilia Then</creatorcontrib><creatorcontrib>de St. Aubin, Michael</creatorcontrib><creatorcontrib>Restrepo, Angela Cadavid</creatorcontrib><creatorcontrib>Mayfield, Helen</creatorcontrib><creatorcontrib>Dumas, Devan</creatorcontrib><creatorcontrib>Finch, Emilie</creatorcontrib><creatorcontrib>Garnier, Salome</creatorcontrib><creatorcontrib>Etienne, Marie Caroline</creatorcontrib><creatorcontrib>Iselin, Louisa</creatorcontrib><creatorcontrib>Duke, William</creatorcontrib><creatorcontrib>Jarolim, Petr</creatorcontrib><creatorcontrib>Oasan, Timothy</creatorcontrib><creatorcontrib>Yu, Jingyou</creatorcontrib><creatorcontrib>Wan, Huahua</creatorcontrib><creatorcontrib>Peña, Farah</creatorcontrib><creatorcontrib>Iihoshi, Naomi</creatorcontrib><creatorcontrib>Abdalla, Gabriela</creatorcontrib><creatorcontrib>Lopez, Beatriz</creatorcontrib><creatorcontrib>Cruz, Lucia de la</creatorcontrib><creatorcontrib>Henríquez, Bernarda</creatorcontrib><creatorcontrib>Espinosa-Bode, Andres</creatorcontrib><creatorcontrib>Puello, Yosanly Cornelio</creatorcontrib><creatorcontrib>Durski, Kara</creatorcontrib><creatorcontrib>Baldwin, Margaret</creatorcontrib><creatorcontrib>Baez, Amado Alejandro</creatorcontrib><creatorcontrib>Merchant, Roland C.</creatorcontrib><creatorcontrib>Barouch, Dan H.</creatorcontrib><creatorcontrib>Skewes-Ramm, Ronald</creatorcontrib><creatorcontrib>Gutiérrez, Emily Zielinski</creatorcontrib><creatorcontrib>Kucharski, Adam</creatorcontrib><creatorcontrib>Lau, Colleen L.</creatorcontrib><title>SARS-CoV-2 seroprevalence, cumulative infections, and immunity to symptomatic infection – A multistage national household survey and modelling study, Dominican Republic, June–October 2021</title><title>Lancet Regional Health - Americas (Online)</title><addtitle>Lancet Reg Health Am</addtitle><description>Population-level SARS-CoV-2 immunological protection is poorly understood but can guide vaccination and non-pharmaceutical intervention priorities. Our objective was to characterise cumulative infections and immunological protection in the Dominican Republic.
Household members ≥5 years were enrolled in a three-stage national household cluster serosurvey in the Dominican Republic. We measured pan-immunoglobulin antibodies against the SARS-CoV-2 spike (anti-S) and nucleocapsid glycoproteins, and pseudovirus neutralising activity against the ancestral and B.1.617.2 (Delta) strains. Seroprevalence and cumulative prior infections were weighted and adjusted for assay performance and seroreversion. Binary classification machine learning methods and pseudovirus neutralising correlates of protection were used to estimate 50% and 80% protection against symptomatic infection.
Between 30 Jun and 12 Oct 2021 we enrolled 6683 individuals from 3832 households. We estimate that 85.0% (CI 82.1–88.0) of the ≥5 years population had been immunologically exposed and 77.5% (CI 71.3–83) had been previously infected. Protective immunity sufficient to provide at least 50% protection against symptomatic SARS-CoV-2 infection was estimated in 78.1% (CI 74.3–82) and 66.3% (CI 62.8–70) of the population for the ancestral and Delta strains respectively. Younger (5–14 years, OR 0.47 [CI 0.36–0.61]) and older (≥75-years, 0.40 [CI 0.28–0.56]) age, working outdoors (0.53 [0.39–0.73]), smoking (0.66 [0.52–0.84]), urban setting (1.30 [1.14–1.49]), and three vs no vaccine doses (18.41 [10.69–35.04]) were associated with 50% protection against the ancestral strain.
Cumulative infections substantially exceeded prior estimates and overall immunological exposure was high. After controlling for confounders, markedly lower immunological protection was observed to the ancestral and Delta strains across certain subgroups, findings that can guide public health interventions and may be generalisable to other settings and viral strains.
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Our objective was to characterise cumulative infections and immunological protection in the Dominican Republic.
Household members ≥5 years were enrolled in a three-stage national household cluster serosurvey in the Dominican Republic. We measured pan-immunoglobulin antibodies against the SARS-CoV-2 spike (anti-S) and nucleocapsid glycoproteins, and pseudovirus neutralising activity against the ancestral and B.1.617.2 (Delta) strains. Seroprevalence and cumulative prior infections were weighted and adjusted for assay performance and seroreversion. Binary classification machine learning methods and pseudovirus neutralising correlates of protection were used to estimate 50% and 80% protection against symptomatic infection.
Between 30 Jun and 12 Oct 2021 we enrolled 6683 individuals from 3832 households. We estimate that 85.0% (CI 82.1–88.0) of the ≥5 years population had been immunologically exposed and 77.5% (CI 71.3–83) had been previously infected. Protective immunity sufficient to provide at least 50% protection against symptomatic SARS-CoV-2 infection was estimated in 78.1% (CI 74.3–82) and 66.3% (CI 62.8–70) of the population for the ancestral and Delta strains respectively. Younger (5–14 years, OR 0.47 [CI 0.36–0.61]) and older (≥75-years, 0.40 [CI 0.28–0.56]) age, working outdoors (0.53 [0.39–0.73]), smoking (0.66 [0.52–0.84]), urban setting (1.30 [1.14–1.49]), and three vs no vaccine doses (18.41 [10.69–35.04]) were associated with 50% protection against the ancestral strain.
Cumulative infections substantially exceeded prior estimates and overall immunological exposure was high. After controlling for confounders, markedly lower immunological protection was observed to the ancestral and Delta strains across certain subgroups, findings that can guide public health interventions and may be generalisable to other settings and viral strains.
This study was funded by the US CDC.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36408529</pmid><doi>10.1016/j.lana.2022.100390</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3594-4330</orcidid><orcidid>https://orcid.org/0000-0002-8399-9205</orcidid><orcidid>https://orcid.org/0000-0001-7308-6552</orcidid><orcidid>https://orcid.org/0000-0002-2355-3586</orcidid><orcidid>https://orcid.org/0000-0001-7044-5257</orcidid><orcidid>https://orcid.org/0000-0003-1353-9948</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
title | SARS-CoV-2 seroprevalence, cumulative infections, and immunity to symptomatic infection – A multistage national household survey and modelling study, Dominican Republic, June–October 2021 |
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