Evidence map›Paper›PMID 36370196›Full record

ArticleMedical microbiology and immunology2023

Reduced neutralization against Delta, Gamma, Mu, and Omicron BA.1 variants of SARS-CoV-2 from previous non-Omicron infection.

Paola Pidal, Jorge Fernández, Constanza Airola, Miguel Araujo, Ana María Menjiba, Héctor San Martín, Nicole Bruneau, Monserrat Balanda, Coral Elgueta, Rodrigo Fasce and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Medical microbiology and immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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  4. Cross-reactive humoral and CD4Frontiers in immunology · 2023
    Article
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

13 authors at 3 institutions in 1 country.

Paola PidalMicrobiología y Control de infecciones asociadas a la atención en Salud, Clínica Indisa, Santiago, Chile.
Jorge FernándezSubdepartment of Molecular Genetics, Instituto de Salud Pública de Chile, Santiago, Chile.
Constanza AirolaEpidemiología y Control de infecciones asociadas a la atención en Salud, Clínica Indisa, Santiago, Chile.
Miguel AraujoUnidad de Calidad, Clínica Indisa, Santiago, Chile.
Ana María MenjibaUnidad de Calidad, Clínica Indisa, Santiago, Chile.
Héctor San MartínSection of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
Nicole BruneauSection of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
Monserrat BalandaSection of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
Coral ElguetaSection of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
Rodrigo FasceSubdepartment of Viral Diseases, Instituto de Salud Pública de Chile, Santiago, Chile.
María Teresa ValenzuelaDepartment of Epidemiology and Public Health, Faculty Medicine, Universidad de los Andes, Santiago, Chile.
Ariel OrellanaFacultad de Ciencias de la Vida, Universidad Andrés Bello, Santiago, Chile.
Eugenio RamírezSection of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile. eramirez@ispch.cl.ORCID http://orcid.org/0000-0002-5299-7928
Instituto de Salud Pública de Chile · CLUniversidad Andrés Bello · CLUniversidad de Los Andes, Chile · CL

Funding

ANID de Chile COVID0557
6 · The paper itself

Abstract

The understanding of the host immune response to SARS-CoV-2 variants of concern is critical for improving diagnostics, therapy development, and vaccines. Here, we analyzed the level of neutralizing antibodies against SARS-CoV-2 D614G, Delta, Gamma, Mu, and Omicron variants in D614G infected healthcare workers during a follow-up up to 6 months after recovery. We followed up 76 patients: 60.5% were women and 39.5% men. The 96.1% and 3.9% were symptomatic and asymptomatic, respectively. The most frequent symptoms were headache, myalgia, and cough. The 65.8%, 65.8%, and 92.1% of the infected individuals were positive for neutralizing antibodies against D614G variant at 2, 4, and 6 months of follow-up, respectively. The 26.3%, 48.7% and 65.8% of patients neutralized Delta variant, 19.7%, 32.9% and 52.6% of patients neutralized Gamma, 7.9%, 19.7% and 44.7% of patients neutralized Mu, and 4.0%, 9.2% and 15.8% of patients neutralized Omicron. Low neutralization against Gamma and Mu variants was observed during the follow-up, and very low against the Omicron variant was detected during the same period. The median of neutralizing antibody titers against D614G and Delta variants increased significantly during the follow-up. An association was observed between the levels of neutralizing antibodies against D614G and Delta variants and the severity of the disease. Our results suggest an immune escape from neutralizing antibodies with the Omicron variant because of the many mutations localized in the S protein.

Indexed as

COVID-19SARS-CoV-2Antibodies, NeutralizingAntibodies, ViralFemaleHumansMaleAntibodies, NeutralizingAntibodies, ViralDelta variantFollow-up immune responseGamma variantMu variantNeutralizing antibodiesOmicron SARS-CoV-2 variant

Identifiers

PMID36370196
PMCPMC9660018
OpenAlexW4308897590

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.