Evidence map›Paper›PMID 37729215›Full record

ArticlePloS one2023

Discovery of neutralizing SARS-CoV-2 antibodies enriched in a unique antigen specific B cell cluster.

Stine Sofie Frank Lende, Nanna Møller Barnkob, Randi Westh Hansen, Harsh Bansia, Mike Vestergaard, Frederik Holm Rothemejer, Anne Worsaae, Deijona Brown, Maria Lange Pedersen, Anna Halling Folkmar Rahimic and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Monoclonal Antibody Generation Using Single B Cell Screening for Treating Infectious Diseases.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    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

18 authors at 5 institutions in 3 countries.

Stine Sofie Frank LendeDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Nanna Møller BarnkobSymphogen, Ballerup, Denmark.ORCID 0000-0003-2932-5063
Randi Westh HansenSymphogen, Ballerup, Denmark.
Harsh BansiaStructural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States of America.
Mike VestergaardSymphogen, Ballerup, Denmark.
Frederik Holm RothemejerDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Anne WorsaaeSymphogen, Ballerup, Denmark.
Deijona BrownStructural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States of America.ORCID 0009-0003-0508-1057
Maria Lange PedersenDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Anna Halling Folkmar RahimicDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-0681-3611
Anna Karina JuhlDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Torben GjettingStructural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States of America.
Lars ØstergaardDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Amédée Des GeorgesStructural Biology Initiative, CUNY Advanced Science Research Center, New York, NY, United States of America.
Laurent-Michel VuillardServier, Suresnes, France.
Mariane Høgsbjerg SchleimannDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.
Klaus KoefoedSymphogen, Ballerup, Denmark.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital, Skejby, Denmark.ORCID 0000-0001-7020-5173
Aarhus University · DKSymphogen (Denmark) · DKThe Graduate Center, CUNY · USAarhus University Hospital · DKServier (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite development of effective SARS-CoV-2 vaccines, a sub-group of vaccine non-responders depends on therapeutic antibodies or small-molecule drugs in cases of severe disease. However, perpetual viral evolution has required continuous efficacy monitoring as well as exploration of new therapeutic antibodies, to circumvent resistance mutations arising in the viral population. We performed SARS-CoV-2-specific B cell sorting and subsequent single-cell sequencing on material from 15 SARS-CoV-2 convalescent participants. Through screening of 455 monoclonal antibodies for SARS-CoV-2 variant binding and virus neutralization, we identified a cluster of activated B cells highly enriched for SARS-CoV-2 neutralizing antibodies. Epitope binning and Cryo-EM structure analysis identified the majority of neutralizing antibodies having epitopes overlapping with the ACE2 receptor binding motif (class 1 binders). Extensive functional antibody characterization identified two potent neutralizing antibodies, one retaining SARS-CoV-1 neutralizing capability, while both bind major common variants of concern and display prophylactic efficacy in vivo. The transcriptomic signature of activated B cells harboring broadly binding neutralizing antibodies with therapeutic potential identified here, may be a guide in future efforts of rapid therapeutic antibody discovery.

Indexed as

Blood Group AntigensCOVID-19Antibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesEpitopesHumansSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralBlood Group AntigensCOVID-19 VaccinesEpitopes

Identifiers

PMID37729215
PMCPMC10511142
OpenAlexW4386884075

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.