Evidence map›Paper›PMID 28949917›Full record

ArticleeLife2017

A potent human neutralizing antibody Fc-dependently reduces established HBV infections.

Dan Li, Wenhui He, Ximing Liu, Sanduo Zheng, Yonghe Qi, Huiyu Li, Fengfeng Mao, Juan Liu, Yinyan Sun, Lijing Pan and 4 more

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing 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

74 citing papers in PubMed.

  1. Trial
  2. Article
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  5. Acid-sensing ion channels as sensors of brain metabolic state.Pflugers Archiv : European journal of physiology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. A CD25×TIGIT bispecific antibody induces anti-tumor activity through selective intratumoral Treg cell depletion.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  15. LRG1 promotes atherosclerosis by inducing macrophage M1-like polarization.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Hepatitis B: Model Systems and Therapeutic Approaches.Journal of immunology research · 2024
    Review
  20. The Culprit Behind HBV-Infected Hepatocytes: NTCP.Drug design, development and therapy · 2024
    Review

14 more citing papers are in PubMed but not listed here.

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

14 authors.

Dan LiPeking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program, School of Life Sciences, Tsinghua University, Beijing, China.ORCID 0000-0002-3670-4056
Wenhui HeNational Institute of Biological Sciences, Beijing, China.
Ximing LiuNational Institute of Biological Sciences, Beijing, China.
Sanduo ZhengNational Institute of Biological Sciences, Beijing, China.
Yonghe QiNational Institute of Biological Sciences, Beijing, China.
Huiyu LiNational Institute of Biological Sciences, Beijing, China.
Fengfeng MaoNational Institute of Biological Sciences, Beijing, China.
Juan LiuNational Institute of Biological Sciences, Beijing, China.
Yinyan SunNational Institute of Biological Sciences, Beijing, China.
Lijing PanPeking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program, School of Life Sciences, Tsinghua University, Beijing, China.
Kaixin DuNational Institute of Biological Sciences, Beijing, China.
Keqiong YeNational Institute of Biological Sciences, Beijing, China.ORCID 0000-0001-6169-7049
Wenhui LiNational Institute of Biological Sciences, Beijing, China.ORCID 0000-0003-1305-7404
Jianhua SuiNational Institute of Biological Sciences, Beijing, China.ORCID 0000-0002-1272-9662

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus (HBV) infection is a major global health problem. Currently-available therapies are ineffective in curing chronic HBV infection. HBV and its satellite hepatitis D virus (HDV) infect hepatocytes via binding of the preS1 domain of its large envelope protein to sodium taurocholate cotransporting polypeptide (NTCP). Here, we developed novel human monoclonal antibodies that block the engagement of preS1 with NTCP and neutralize HBV and HDV with high potency. One antibody, 2H5-A14, functions at picomolar level and exhibited neutralization-activity-mediated prophylactic effects. It also acts therapeutically by eliciting antibody-Fc-dependent immunological effector functions that impose durable suppression of viral infection in HBV-infected mice, resulting in reductions in the levels of the small envelope antigen and viral DNA, with no emergence of escape mutants. Our results illustrate a novel antibody-Fc-dependent approach for HBV treatment and suggest 2H5-A14 as a novel clinical candidate for HBV prevention and treatment of chronic HBV infection.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralAntiviral AgentsChemopreventionDisease Models, AnimalHepatitis BHepatitis B virusHepatitis Delta VirusHumansImmunotherapyMiceTreatment OutcomeAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralAntiviral Agentsantibodyeffector functionFc receptorHBVimmunologyinfectious diseasemicrobiologymouseNTCPpreS1virus

Identifiers

PMID28949917
PMCPMC5614562

What OpenQuestion holds

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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.