Evidence map›Paper›PMID 34780883›Full record

ArticleVirus research2022

Reduced levels of convalescent neutralizing antibodies against SARS-CoV-2 B.1+L249S+E484K lineage.

Diego A Álvarez-Díaz, Katherine Laiton-Donato, Orlando Alfredo Torres-García, Hector Alejandro Ruiz-Moreno, Carlos Franco-Muñoz, Maria Angie Beltran, Marcela Mercado-Reyes, Miguel Germán Rueda, Ana Luisa Muñoz

Abstract read
In one paragraph

Article in Virus research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  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

9 authors.

Diego A Álvarez-DíazGrupo de Genómica de Microorganismos Emergentes, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia.
Katherine Laiton-DonatoGrupo de Genómica de Microorganismos Emergentes, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia.
Orlando Alfredo Torres-GarcíaFaculty of Veterinary Medicine and Zootechnics, Universidad Antonio Nariño, Bogotá, Colombia.
Hector Alejandro Ruiz-MorenoGrupo de Genómica de Microorganismos Emergentes, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia.
Carlos Franco-MuñozGrupo de Genómica de Microorganismos Emergentes, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia; Grupo de Parasitología, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia.
Maria Angie BeltranFundación Banco Nacional de Sangre Hemolife, Bogotá, Colombia.
Marcela Mercado-ReyesGrupo de Genómica de Microorganismos Emergentes, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, Colombia.
Miguel Germán RuedaFundación Banco Nacional de Sangre Hemolife, Bogotá, Colombia.
Ana Luisa MuñozFundación Banco Nacional de Sangre Hemolife, Bogotá, Colombia; Faculty of Science, Universidad Antonio Nariño, Calle 23 #116-31, Bodega 26, Bogotá, Colombia. Electronic address: ana.munoz@hemolfeamerica.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The E484K mutation at the SARS-CoV-2 Spike protein emerged independently in different variants around the world and has been widely associated with immune escape from neutralizing antibodies generated during previous infection or vaccination. In this work, the B.1 + L249S+E484K lineage was isolated along with A.1, B.1.420, and B.1.111 SARS-CoV-2 lineages without the E484K mutation and the neutralizing titer of convalescent sera was compared using microneutralization assays. While no significant differences in the neutralizing antibody titers were found between A.1 and B.lineages without the E484K mutation, the neutralizing titers against B.1 + L249S+E484K were 1.5, 1.9, 2.1, and 1.3-fold lower than against A.1, B.1.420, B.1.111-I, and B.1.111-II, respectively. However, molecular epidemiological data indicate that there is no increase in the transmissibility rate associated with this new lineage. This study supports the capability of new variants with the E484K mutation to be resistant to neutralization by humoral immunity, and therefore the need to intensify surveillance programs to determine if these lineages represent a risk for public health.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19Spike Glycoprotein, CoronavirusHumansImmunity, HumoralMutationSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19E484k mutationNeutralizing antibodiesSARS-CoV-2 lineagesSpike proteinVariant of Interest

Identifiers

PMID34780883
PMCPMC8585963

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.