Evidence map›Paper›PMID 35263223›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Induction of broadly neutralizing antibodies using a secreted form of the hepatitis C virus E1E2 heterodimer as a vaccine candidate.

Ruixue Wang, Saori Suzuki, Johnathan D Guest, Brigitte Heller, Maricar Almeda, Alexander K Andrianov, Alexander Marin, Roy A Mariuzza, Zhen-Yong Keck, Steven K H Foung and 5 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Ruixue WangInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
Saori SuzukiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08540.ORCID 0000-0001-5233-6604
Johnathan D GuestInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.ORCID 0000-0003-1521-5242
Brigitte HellerDepartment of Molecular Biology, Princeton University, Princeton, NJ 08540.
Maricar AlmedaDepartment of Molecular Biology, Princeton University, Princeton, NJ 08540.
Alexander K AndrianovInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
Alexander MarinInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
Roy A MariuzzaInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
Zhen-Yong KeckDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0002-1275-7495
Steven K H FoungDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0001-7149-6160
Abdul S YunusInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
Brian G PierceInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.ORCID 0000-0003-4821-0368
Eric A TothInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.ORCID 0000-0002-0766-5131
Alexander PlossDepartment of Molecular Biology, Princeton University, Princeton, NJ 08540.ORCID 0000-0001-9322-7252
Thomas R FuerstInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850.
University of Maryland, Baltimore · USPrinceton University · USStanford University · US

Funding

Rational design and efficacy testing of vaccines against HCVR01AI168048 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI Alexander Andrianov, Thomas R Fuerst · 2022 to 2026
$7.1M
Genetic Viral and Host Adaptations to Breach Species Barriers of HCVR01AI107301 · NIAID · PRINCETON UNIVERSITY · PI Thomas Pietschmann, Alexander Ploss · 2013 to 2026
$6.0M
Structure-Based Vaccine Design for Hepatits C VirusR01AI132213 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI ANDRIANOV, ALEXANDER, FOUNG, STEVEN · 2017 to 2021
$6.0M
Project 2 - FranceU19AI123862 · NIAID · STANFORD UNIVERSITY · PI FOUNG, STEVEN · 2016 to 2020
$3.9M
Design of immunologically intact soluble HCV E1E2 complexes using transmembrane-mimic scaffoldsR21AI154100 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI FUERST, THOMAS R, PIERCE, BRIAN G. · 2020 to 2021
$422k
NIAID NIH HHS R01 AI107301NIAID NIH HHS R01 AI132213NIAID NIH HHS R01 AI168048NIAID NIH HHS R21 AI154100NIAID NIH HHS U19 AI123862
6 · The paper itself

Abstract

SignificanceHepatitis C virus chronically infects approximately 1% of the world's population, making an effective vaccine for hepatitis C virus a major unmet public health need. The membrane-associated E1E2 envelope glycoprotein has been used in clinical studies as a vaccine candidate. However, limited neutralization breadth and difficulty in producing large amounts of homogeneous membrane-associated E1E2 have hampered efforts to develop an E1E2-based vaccine. Our previous work described the design and biochemical validation of a native-like soluble secreted form of E1E2 (sE1E2). Here, we describe the immunogenic characterization of the sE1E2 complex. sE1E2 elicited broadly neutralizing antibodies in immunized mice, with increased neutralization breadth relative to the membrane-associated E1E2, thereby validating this platform as a promising model system for vaccine development.

Indexed as

Broadly Neutralizing AntibodiesHepatitis CHepatitis C AntibodiesImmunogenicity, VaccineViral Envelope ProteinsViral Hepatitis VaccinesAnimalsMiceProtein MultimerizationBroadly Neutralizing AntibodiesE1 protein, Hepatitis C virusglycoprotein E2, Hepatitis C virusHepatitis C AntibodiesViral Envelope ProteinsViral Hepatitis VaccinesE1E2 envelope glycoproteinshepatitis C virussecretedvaccine

Identifiers

PMID35263223
PMCPMC8931252
OpenAlexW4220998122

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.