Evidence map›Paper›PMID 32579155›Full record

ArticleThe Journal of experimental medicine2020

Potent human broadly neutralizing antibodies to hepatitis B virus from natural controllers.

Verena Hehle, Maxime Beretta, Maryline Bourgine, Malika Ait-Goughoulte, Cyril Planchais, Solen Morisse, Benjamin Vesin, Valérie Lorin, Thierry Hieu, Andrea Stauffer and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  8. Targeting HBV with RNA interference: Paths to cure.Science translational medicine · 2025
    Review
  9. Article
  10. [Research progress on B cells in chronic hepatitis B].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 2 countries.

Verena HehleLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Maxime BerettaLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Maryline BourgineMolecular Virology and Vaccinology Unit, Institut Pasteur, Paris, France.
Malika Ait-GoughoulteRoche Innovation Center, Basel, Switzerland.
Cyril PlanchaisLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Solen MorisseMolecular Virology and Vaccinology Unit, Institut Pasteur, Paris, France.
Benjamin VesinMolecular Virology and Vaccinology Unit, Institut Pasteur, Paris, France.
Valérie LorinLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Thierry HieuLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Andrea StaufferRoche Innovation Center, Basel, Switzerland.
Oriane FiquetInnate Immunity Unit, Department of Immunology, Paris, France.
Jordan D DimitrovCentre de Recherche des Cordeliers, Institut National de la Santé et de la Recherche Médicale, Sorbonne Université, Université de Paris, Paris, France.
Marie-Louise MichelInstitut Pasteur, Paris, France.
Marie-Noëlle UngeheuerInvestigation Clinique et Accès aux Ressources Biologiques platform, Center for Translational Science, Institut Pasteur, Paris, France.
Camille SureauInstitut National de la Transfusion Sanguine, Centre National de la Recherche-Institut National de la Santé et de la Recherche Médicale U1134, Paris, France.
Stanislas PolInstitut National de la Santé et de la Recherche Médicale U1223, Institut Pasteur, Paris, France.
James P Di SantoInnate Immunity Unit, Department of Immunology, Paris, France.
Hélène Strick-MarchandInnate Immunity Unit, Department of Immunology, Paris, France.
Nadège PelletierRoche Innovation Center, Basel, Switzerland.
Hugo MouquetLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, Paris, France.
Inserm · FRInstitut Pasteur · FRRoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare individuals can naturally clear chronic hepatitis B virus (HBV) infection and acquire protection from reinfection as conferred by vaccination. To examine the protective humoral response against HBV, we cloned and characterized human antibodies specific to the viral surface glycoproteins (HBsAg) from memory B cells of HBV vaccinees and controllers. We found that human HBV antibodies are encoded by a diverse set of immunoglobulin genes and recognize various conformational HBsAg epitopes. Strikingly, HBsAg-specific memory B cells from natural controllers mainly produced neutralizing antibodies able to cross-react with several viral genotypes. Furthermore, monotherapy with the potent broadly neutralizing antibody Bc1.187 suppressed viremia in vivo in HBV mouse models and led to post-therapy control of the infection in a fraction of animals. Thus, human neutralizing HBsAg antibodies appear to play a key role in the spontaneous control of HBV and represent promising immunotherapeutic tools for achieving HBV functional cure in chronically infected humans.

Indexed as

AnimalsAntibodies, NeutralizingB-LymphocytesCross ReactionsEnzyme-Linked Immunosorbent AssayEpitopesFlow CytometryHepatitis BHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B VaccinesHepatitis B virusHumansImmunologic MemoryMiceNeutralization TestsAntibodies, NeutralizingEpitopesHepatitis B Surface AntigensHepatitis B Vaccines

Identifiers

PMID32579155
PMCPMC7537403
OpenAlexW3037698050

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.