Evidence map›Paper›PMID 38711498›Full record

ArticleFrontiers in immunology2024

CARs derived from broadly neutralizing, human monoclonal antibodies identified by single B cell sorting target hepatitis B virus-positive cells.

Sophia Schreiber, Lisa S Dressler, Eva Loffredo-Verde, Theresa Asen, Stephanie Färber, Wenshi Wang, Tanja Groll, Anindita Chakraborty, Fenna Kolbe, Christoph Kreer and 6 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. 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
–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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

16 authors.

Sophia Schreiber *Institute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Lisa S Dressler *Institute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Eva Loffredo-VerdeInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Theresa AsenInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Stephanie FärberInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Wenshi WangDepartment of Infectious Diseases, Molecular Virology, University Hospital, Heidelberg, Germany.
Tanja GrollInstitute of Pathology, School of Medicine, Technical University of Munich, Munich, Germany.
Anindita ChakrabortyInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Fenna KolbeInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Christoph KreerLaboratory of Experimental Immunology, Institute of Virology, University of Cologne, Faculty of Medicine and University Hospital of Cologne, Cologne, Germany.
Anna D KosinskaInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.
Sylvain SimonTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, United States.
Stephan UrbanDepartment of Infectious Diseases, Molecular Virology, University Hospital, Heidelberg, Germany.
Florian KleinLaboratory of Experimental Immunology, Institute of Virology, University of Cologne, Faculty of Medicine and University Hospital of Cologne, Cologne, Germany.
Stanley R RiddellTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, United States.
Ulrike ProtzerInstitute of Virology, School of Medicine, Technical University of Munich / Helmholtz Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To design new CARs targeting hepatitis B virus (HBV), we isolated human monoclonal antibodies recognizing the HBV envelope proteins from single B cells of a patient with a resolved infection. HBV-specific memory B cells were isolated by incubating peripheral blood mononuclear cells with biotinylated hepatitis B surface antigen (HBsAg), followed by single-cell flow cytometry-based sorting of live, CD19

Indexed as

Hepatitis B Surface AntigensHepatitis B virusAnimalsAntibodies, MonoclonalB-LymphocytesBroadly Neutralizing AntibodiesHepatitis BHumansImmunotherapy, AdoptiveMiceReceptors, Chimeric AntigenT-LymphocytesAntibodies, MonoclonalBroadly Neutralizing AntibodiesHepatitis B Surface AntigensReceptors, Chimeric Antigenbroad neutralizationchimeric antigen receptorHBsAghepatitis B virus envelope proteinshuman monoclonal antibodylinear epitopesingle B cell sortingtonic signaling

Identifiers

PMID38711498
PMCPMC11072186

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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.