Evidence map›Paper›PMID 38454385›Full record

ArticleBMC medicine2024

Correlates of protection and determinants of SARS-CoV-2 breakthrough infections 1 year after third dose vaccination.

Carla Martín Pérez, Ruth Aguilar, Alfons Jiménez, Gemma Salmerón, Mar Canyelles, Rocío Rubio, Marta Vidal, Inocencia Cuamba, Diana Barrios, Natalia Díaz and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

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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

21 authors at 6 institutions in 3 countries.

Carla Martín PérezISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Ruth AguilarISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Alfons JiménezISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Gemma SalmerónOccupational Health Department, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Mar CanyellesISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Rocío RubioISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Marta VidalISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Inocencia CuambaISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Diana BarriosISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Natalia DíazISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Rebeca SantanoISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Pau SerraInstitut d'Investigacions Biomèdiques August Pi Sunyer (IDIBAPS), Barcelona, 08036, Spain.
Pere SantamariaInstitut d'Investigacions Biomèdiques August Pi Sunyer (IDIBAPS), Barcelona, 08036, Spain.
Luis IzquierdoISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Antoni TrillaISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Anna VilellaISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Sonia BarrosoOccupational Health Department, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Marta TortajadaOccupational Health Department, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Alberto L García-BasteiroISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain.
Gemma Moncunill *ISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain. gemma.moncunill@isglobal.org.
Carlota Dobaño *ISGlobal, Hospital Clínic, Universitat de Barcelona, Barcelona, 08036, Spain. carlota.dobano@isglobal.org.ORCID 0000-0002-6751-4060
Barcelona Institute for Global Health · ESCentro de Investigación en Red en Enfermedades Cardiovasculares · ESUniversitat de Barcelona · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESManhiça Health Research Centre · MZUniversity of Calgary · CA

Funding

AGAUR 100046TC21_ 2022 INV-1 00046Departament de Salut, Generalitat de Catalunya PERIS SLT017/20/000224European Social Fund RYC 2020-538 029886-I/AEI/10.13039/501100011033European Union 101046314Ministerio de Ciencia e Innovación CEX2018-000806-SMinisterio de Ciencia e Innovación PID2021-125493OB-I00
6 · The paper itself

Abstract

backgroundThe emergence of new SARS-CoV-2 variants and the waning of immunity raise concerns about vaccine effectiveness and protection against COVID-19. While antibody response has been shown to correlate with the risk of infection with the original variant and earlier variants of concern, the effectiveness of antibody-mediated protection against Omicron and the factors associated with protection remain uncertain.

methodsWe evaluated antibody responses to SARS-CoV-2 spike (S) and nucleocapsid (N) antigens from Wuhan and variants of concern by Luminex and their role in preventing breakthrough infections 1 year after a third dose of mRNA vaccination, in a cohort of health care workers followed since the pandemic onset in Spain (N = 393). Data were analyzed in relation to COVID-19 history, demographic factors, comorbidities, vaccine doses, brand, and adverse events.

resultsHigher levels of anti-S IgG and IgA to Wuhan, Delta, and Omicron were associated with protection against vaccine breakthroughs (IgG against Omicron S antigen HR, 0.06, 95%CI, 0.26-0.01). Previous SARS-CoV-2 infection was positively associated with antibody levels and protection against breakthroughs, and a longer time since last infection was associated with lower protection. In addition, priming with BNT162b2 followed by mRNA-1273 booster was associated with higher antibody responses than homologous mRNA-1273 vaccination.

conclusionsData show that IgG and IgA induced by vaccines against the original strain or by hybrid immunization are valid correlates of protection against Omicron BA.1 despite immune escape and support the benefits of heterologous vaccination regimens to enhance antibodies and the prioritization of booster vaccination in individuals without recent infections.

Indexed as

COVID-192019-nCoV Vaccine mRNA-1273Antibodies, ViralBNT162 VaccineBreakthrough InfectionsHumansImmunoglobulin AImmunoglobulin GSARS-CoV-2Vaccination2019-nCoV Vaccine mRNA-1273Antibodies, ViralBNT162 VaccineImmunoglobulin AImmunoglobulin GAntibody responseBreakthrough infectionsCorrelates of protectionOmicronSARS-CoV-2

Identifiers

PMID38454385
PMCPMC10921636
OpenAlexW4392637047

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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.