Evidence map›Paper›PMID 31809638›Full record

ArticleHuman vaccines & immunotherapeutics2020

Designing a therapeutic hepatitis B vaccine to circumvent immune tolerance.

D C Whitacre, C J Peters, C Sureau, K Nio, F Li, L Su, J E Jones, M Isogawa, M Sallberg, L Frelin and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Hepatitis B eradication: vaccine as a key player.American journal of translational research · 2023
    Review
  9. [Hepatitis B vaccines-history, achievements, challenges, and perspectives].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Hepatitis B vaccine development and implementation.Human vaccines & immunotherapeutics · 2020
    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

12 authors at 8 institutions in 4 countries.

D C WhitacreDepartment of Immunology, VLP Biotech, Inc., JLABS San Diego, San Diego, CA, USA.ORCID 0000-0003-3803-9157
C J PetersDepartment of Immunology, VLP Biotech, Inc., JLABS San Diego, San Diego, CA, USA.
C SureauMolecular Virology Laboratory, Institut National de la Transfusion Sanguine (INTS), Paris, France.
K NioGraduate School of Medicine, Department of Gastroenterology, Kanazawa University, Kanazawa, Ishikawa, Japan.
F LiLineberger Comprehensive Cancer Center, Department of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
L SuLineberger Comprehensive Cancer Center, Department of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
J E JonesDepartment of Immunology, VLP Biotech, Inc., JLABS San Diego, San Diego, CA, USA.
M IsogawaDepartment of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
M SallbergDepartment of Laboratory Medicine, Division of Clinical Microbiology, F68, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockhold, Sweden.
L FrelinDepartment of Laboratory Medicine, Division of Clinical Microbiology, F68, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockhold, Sweden.
D L PetersonDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA, USA.
D R MilichDepartment of Immunology, VLP Biotech, Inc., JLABS San Diego, San Diego, CA, USA.
Vaccine Research Institute of San Diego · USKarolinska University Hospital · SEUniversity of North Carolina at Chapel Hill · USInstitut National de la Transfusion Sanguine · FRKanazawa University · JPNagoya City University · JPVirginia Commonwealth University · USVLP Biotech (United States) · US

Funding

A Therapeutic Vaccine for Chronic Hepatitis BR44AI088919 · NIAID · VLP BIOTECH, INC. · PI MILICH, DAVID R. · 2012 to 2020
$4.6M
DEVELOPMENT OF THE HBCAG AS A VACCINE CARRIER PLATFORMR01AI049730 · NIAID · VACCINE RESEARCH INSTITUTE OF SAN DIEGO · PI MILICH, DAVID R. · 2000 to 2008
$3.6M
NIAID NIH HHS R01 AI049730NIAID NIH HHS R44 AI088919
6 · The paper itself

Abstract

An effective prophylactic hepatitis B virus (HBV) vaccine has long been available but is ineffective for chronic infection. The primary cause of chronic hepatitis B (CHB) and greatest impediment for a therapeutic vaccine is the direct and indirect effects of immune tolerance to HBV antigens. The resulting defective CD4

Indexed as

Hepatitis BHepatitis B, ChronicAnimalsCD8-Positive T-LymphocytesHepatitis B Core AntigensHepatitis B Surface AntigensHepatitis B VaccinesHepatitis B virusImmune ToleranceMiceHepatitis B Core AntigensHepatitis B Surface AntigensHepatitis B VaccinesHbvimmune toleranceneutralizing antibodypres1therapeutic vaccine

Identifiers

PMID31809638
PMCPMC7062423
OpenAlexW2992993817

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.