Evidence map›Paper›PMID 39071888›Full record

ArticleiScience2024

Broad sarbecovirus neutralization by combined memory B cell antibodies to ancestral SARS-CoV-2.

Cyril Planchais, Ignacio Fernández, Benjamin Chalopin, Timothée Bruel, Pierre Rosenbaum, Maxime Beretta, Jordan D Dimitrov, Laurine Conquet, Flora Donati, Matthieu Prot and 15 more

Abstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Structural Immunology of SARS-CoV-2.Immunological reviews · 2025
    Review
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

25 authors.

Cyril PlanchaisInstitut Pasteur, Université Paris Cité, INSERM U1222, Humoral Immunology Unit, 75015 Paris, France.
Ignacio FernándezInstitut Pasteur, Université Paris Cité, Structural Virology Unit, 75015 Paris, France.
Benjamin ChalopinCEA, INRAE, Medicines and Healthcare Technologies Department, SIMoS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Timothée BruelCNRS UMR3569, 75015 Paris, France.
Pierre RosenbaumInstitut Pasteur, Université Paris Cité, INSERM U1222, Humoral Immunology Unit, 75015 Paris, France.
Maxime BerettaInstitut Pasteur, Université Paris Cité, INSERM U1222, Humoral Immunology Unit, 75015 Paris, France.
Jordan D DimitrovCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, 75006 Paris, France.
Laurine ConquetInstitut Pasteur, Université Paris Cité, Mouse Genetics Laboratory, 75015 Paris, France.
Flora DonatiInstitut Pasteur, Université Paris Cité, G5 Evolutionary Genomics of RNA Viruses, 75015 Paris, France.
Matthieu ProtInstitut Pasteur, Université Paris Cité, G5 Evolutionary Genomics of RNA Viruses, 75015 Paris, France.
Françoise PorrotCNRS UMR3569, 75015 Paris, France.
Delphine PlanasCNRS UMR3569, 75015 Paris, France.
Isabelle StaropoliCNRS UMR3569, 75015 Paris, France.
Florence Guivel-BenhassineCNRS UMR3569, 75015 Paris, France.
Eduard BaqueroInstitut Pasteur, Université Paris Cité, Structural Virology Unit, 75015 Paris, France.
Sylvie van der WerfCNRS UMR3569, 75015 Paris, France.
Ahmed HaouzInstitut Pasteur, Université Paris Cité, CNRS UMR 3528, Cristallography Platform-C2RT, 75015 Paris, France.
Etienne Simon-LorièreInstitut Pasteur, Université Paris Cité, G5 Evolutionary Genomics of RNA Viruses, 75015 Paris, France.
Xavier MontagutelliInstitut Pasteur, Université Paris Cité, Mouse Genetics Laboratory, 75015 Paris, France.
Bernard MaillèreCEA, INRAE, Medicines and Healthcare Technologies Department, SIMoS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Félix A ReyInstitut Pasteur, Université Paris Cité, Structural Virology Unit, 75015 Paris, France.
Pablo Guardado-CalvoInstitut Pasteur, Université Paris Cité, Structural Virology Unit, 75015 Paris, France.
Hervé NozachCEA, INRAE, Medicines and Healthcare Technologies Department, SIMoS, Université Paris-Saclay, 91190 Gif-sur-Yvette, France.
Olivier SchwartzCNRS UMR3569, 75015 Paris, France.
Hugo MouquetInstitut Pasteur, Université Paris Cité, INSERM U1222, Humoral Immunology Unit, 75015 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies play a pivotal role in protecting from SARS-CoV-2 infection, but their efficacy is challenged by the continuous emergence of viral variants. In this study, we describe two broadly neutralizing antibodies cloned from the memory B cells of a single convalescent individual after infection with ancestral SARS-CoV-2. Cv2.3194, a resilient class 1 anti-RBD antibody, remains active against Omicron sub-variants up to BA.2.86. Cv2.3132, a near pan-Sarbecovirus neutralizer, targets the heptad repeat 2 membrane proximal region. When combined, Cv2.3194 and Cv2.3132 form a complementary SARS-CoV-2 neutralizing antibody cocktail exhibiting a local dose-dependent synergy. Thus, remarkably robust neutralizing memory B cell antibodies elicited in response to ancestral SARS-CoV-2 infection can withstand viral evolution and immune escape. The cooperative effect of such antibody combination may confer a certain level of protection against the latest SARS-CoV-2 variants.

Indexed as

immunologyvirology

Identifiers

PMID39071888
PMCPMC11277385

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.