Evidence map›Paper›PMID 36146515›Full record

ArticleVaccines2022

Predicting SARS-CoV-2 Variant Spread in a Completely Seropositive Population Using Semi-Quantitative Antibody Measurements in Blood Donors.

Lewis Buss, Carlos A Prete, Charles Whittaker, Tassila Salomon, Marcio K Oikawa, Rafael H M Pereira, Isabel C G Moura, Lucas Delerino, Rafael F O Franca, Fabio Miyajima and 31 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

41 authors at 17 institutions in 3 countries.

Lewis BussMRC Centre for Global Infectious Disease Analysis, Imperial College London, London SW7 2BX, UK.ORCID 0000-0002-9009-9301
Carlos A PreteDepartment of Electronic Systems Engineering, University of São Paulo, São Paulo 05508-010, Brazil.
Charles WhittakerMRC Centre for Global Infectious Disease Analysis, Imperial College London, London SW7 2BX, UK.
Tassila SalomonFaculdade Ciências Médicas de Minas Gerais, Belo Horizonte 30130-110, Brazil.ORCID 0000-0002-8123-3118
Marcio K OikawaCenter of Mathematics, Computing and Cognition, Universidade Federal do ABC, Santo André 09210-170, Brazil.ORCID 0000-0003-2416-1864
Rafael H M PereiraInstitute for Applied Economic Research (Ipea), Brasília 70390-025, Brazil.ORCID 0000-0003-2125-7465
Isabel C G MouraFaculdade Ciências Médicas de Minas Gerais, Belo Horizonte 30130-110, Brazil.
Lucas DelerinoFundação Oswaldo Cruz, Rio de Janeiro 21040-900, Brazil.
Rafael F O FrancaFundação Oswaldo Cruz, Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-1846-6007
Fabio MiyajimaFundação Oswaldo Cruz, Rio de Janeiro 21040-900, Brazil.
Alfredo MendroneFundação Pró Sangue Hemocentro de São Paulo (FPS), Sao Paulo 05403-000, Brazil.
Cesar Almeida-NetoFundação Pró Sangue Hemocentro de São Paulo (FPS), Sao Paulo 05403-000, Brazil.ORCID 0000-0002-8490-4634
Nanci A SallesFundação Pró Sangue Hemocentro de São Paulo (FPS), Sao Paulo 05403-000, Brazil.
Suzete C FerreiraFundação Pró Sangue Hemocentro de São Paulo (FPS), Sao Paulo 05403-000, Brazil.
Karine A FladzinskiCentro de Hematologia e Hemoterapia do Paraná (HEMEPAR), Curitiba 80045-145, Brazil.
Luana M de SouzaCentro de Hematologia e Hemoterapia do Paraná (HEMEPAR), Curitiba 80045-145, Brazil.
Luciane K SchierCentro de Hematologia e Hemoterapia do Paraná (HEMEPAR), Curitiba 80045-145, Brazil.
Patricia M InoueCentro de Hematologia e Hemoterapia do Paraná (HEMEPAR), Curitiba 80045-145, Brazil.
Lilyane A XabregasFundação Hospitalar de Hematologia e Hemoterapia do Amazonas (HEMOAM), Manaus 69050-001, Brazil.
Myuki A E CrispimFundação Hospitalar de Hematologia e Hemoterapia do Amazonas (HEMOAM), Manaus 69050-001, Brazil.
Nelson FraijiFundação Hospitalar de Hematologia e Hemoterapia do Amazonas (HEMOAM), Manaus 69050-001, Brazil.ORCID 0000-0001-9662-8887
Luciana M B CarlosCentro de Hematologia e Hemoterapia do Ceará (HEMOCE), Fortaleza 60140-200, Brazil.
Veridiana PessoaCentro de Hematologia e Hemoterapia do Ceará (HEMOCE), Fortaleza 60140-200, Brazil.
Maisa A RibeiroFundação Hemominas, Belo Horizonte 30150-341, Brazil.
Rosenvaldo E de SouzaFundação Hemominas, Belo Horizonte 30150-341, Brazil.
Anna F CavalcanteFundação de Hematologia e Hemoterapia de Pernambuco (HEMOPE), Recife 52011-000, Brazil.
Maria I B ValençaFundação de Hematologia e Hemoterapia de Pernambuco (HEMOPE), Recife 52011-000, Brazil.ORCID 0000-0003-2171-4603
Maria V da SilvaFundação de Hematologia e Hemoterapia de Pernambuco (HEMOPE), Recife 52011-000, Brazil.
Esther LopesInstituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Rio de Janeiro 20211-030, Brazil.
Luiz A FilhoInstituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Rio de Janeiro 20211-030, Brazil.
Sheila O G MateosInstituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Rio de Janeiro 20211-030, Brazil.ORCID 0000-0001-5416-2724
Gabrielle T NunesInstituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Rio de Janeiro 20211-030, Brazil.
David SchlesingerMendelics, São Paulo 02511-000, Brazil.
Sônia Mara Nunes da SilvaFundação Hemominas, Belo Horizonte 30150-341, Brazil.
Alexander L Silva-JuniorFundação Hospitalar de Hematologia e Hemoterapia do Amazonas (HEMOAM), Manaus 69050-001, Brazil.ORCID 0000-0002-5645-252X
Marcia C CastroHarvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
Vítor H NascimentoDepartment of Electronic Systems Engineering, University of São Paulo, São Paulo 05508-010, Brazil.ORCID 0000-0002-0543-4735
Christopher DyeDepartment of Zoology, University of Oxford, Oxford OX1 3SZ, UK.
Michael P BuschVitalant Research Institute, Denver, CO 80230, USA.ORCID 0000-0002-1446-125X
Nuno R FariaMRC Centre for Global Infectious Disease Analysis, Imperial College London, London SW7 2BX, UK.
Ester C SabinoDepartamento de Moléstias Infecciosas e Parasitárias e Instituto de Medicina Tropical da Faculdade de Medicina, Universidade de São Paulo, São Paulo 05508-010, Brazil.ORCID 0000-0003-2623-5126
Fundação Hemopa · BRFundação Hospitalar de Hematologia e Hemoterapia do Amazonas · BRFundação Pró-Sangue Hemocentro de São Paulo · BRHemorio · BRFundação Centro de Hematologia e Hemoterapia de Minas Gerais · BRFaculdade de Ciências Médicas de Minas Gerais · BRFundação Oswaldo Cruz · BRImperial College London · GBUniversidade de São Paulo · BRUniversity of Oxford · GBHarvard University · USHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRInstitute of Applied Economic Research · BRMendelics · BRUniversidade Federal do ABC · BRUniversidade Federal do Ceará · BRUniversity of California, San Francisco · US

Funding

Bill & Melinda Gates Foundation INV- 034540 and INV-034652Bill & Melinda Gates Foundation INV-034540Bill & Melinda Gates Foundation INV-034652Medical Research Council MR/R015600/1Medical Research Council MR/S0195/1Medical Research Council MR/S019510/1NHLBI NIH HHS HHSN268201100007CNHLBI NIH HHS HHSN268201100007ISão Paulo Research Foundation 18/14389-0Wellcome Trust
6 · The paper itself

Abstract

SARS-CoV-2 serologic surveys estimate the proportion of the population with antibodies against historical variants, which nears 100% in many settings. New approaches are required to fully exploit serosurvey data. Using a SARS-CoV-2 anti-Spike (S) protein chemiluminescent microparticle assay, we attained a semi-quantitative measurement of population IgG titers in serial cross-sectional monthly samples of blood donations across seven Brazilian state capitals (March 2021−November 2021). Using an ecological analysis, we assessed the contributions of prior attack rate and vaccination to antibody titer. We compared anti-S titer across the seven cities during the growth phase of the Delta variant and used this to predict the resulting age-standardized incidence of severe COVID-19 cases. We tested ~780 samples per month, per location. Seroprevalence rose to >95% across all seven capitals by November 2021. Driven by vaccination, mean antibody titer increased 16-fold over the study, with the greatest increases occurring in cities with the highest prior attack rates. Mean anti-S IgG was strongly correlated (adjusted R2 = 0.89) with the number of severe cases caused by Delta. Semi-quantitative anti-S antibody titers are informative about prior exposure and vaccination coverage and may also indicate the potential impact of future SARS-CoV-2 variants.

Indexed as

deltaimmunitySARS-CoV-2seroprevalencevaccinesvariants of concern

Identifiers

PMID36146515
PMCPMC9501043
OpenAlexW4294233606

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.