Evidence map›Paper›PMID 35588376›Full record

ArticleThe Journal of clinical investigation2022

Repeated exposure to heterologous hepatitis C viruses associates with enhanced neutralizing antibody breadth and potency.

Nicole Frumento, Alexis Figueroa, Tingchang Wang, Muhammad N Zahid, Shuyi Wang, Guido Massaccesi, Georgia Stavrakis, James E Crowe, Andrew I Flyak, Hongkai Ji and 4 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 3 countries.

Nicole FrumentoDepartment of Medicine and.
Alexis FigueroaDepartment of Medicine and.
Tingchang WangDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
Muhammad N ZahidUniversity of Bahrain, Department of Biology, College of Science, Sakhir Campus, Bahrain.
Shuyi WangDepartment of Medicine and.
Guido MassaccesiDepartment of Medicine and.
Georgia StavrakisDepartment of Medicine and.
James E CroweDepartment of Pathology, Microbiology and Immunology.
Andrew I FlyakDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, USA.
Hongkai JiDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
Stuart C RayDepartment of Medicine and.
George M ShawDepartment of Medicine and.
Andrea L CoxDepartment of Medicine and.
Justin R BaileyDepartment of Medicine and.
Johns Hopkins University · USUniversity of Pennsylvania · USBipar · FRCalifornia Institute of Technology · USUniversity of Bahrain · BH

Funding

The development and pre-clinical assessment of novel HCV vaccines to generate T and B cell immunityU19AI159822 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2021 to 2025
$14.4M
Medical Scientist Training ProgramT32GM136577 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ANDREA L COX · 2020 to 2026
$13.4M
Scientific CoreU19AI088791 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2010 to 2020
$8.2M
Molecular and structural characterization of broadly neutralizing anti-HCV antibodiesR01AI127469 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Justin Richard Bailey · 2017 to 2026
$6.8M
Immunization strategies to elicit broadly neutralizing antibodies against HCVR00AI153465 · NIAID · CORNELL UNIVERSITY · PI FLYAK, ANDREW I · 2022 to 2023
$498k
Development of a single-cell antibody cloning protocol for isolation of hepatitis C virus-specific broadly neutralizing antibodiesR21AI151353 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BAILEY, JUSTIN RICHARD · 2020 to 2021
$450k
NIAID NIH HHS R00 AI153465NIAID NIH HHS R01 AI127469NIAID NIH HHS R21 AI151353NIAID NIH HHS U19 AI088791NIAID NIH HHS U19 AI159822NIGMS NIH HHS T32 GM136577
6 · The paper itself

Abstract

A prophylactic hepatitis C virus (HCV) vaccine that elicits neutralizing antibodies could be key to HCV eradication. However, the genetic and antigenic properties of HCV envelope (E1E2) proteins capable of inducing anti-HCV broadly neutralizing antibodies (bNAbs) in humans have not been defined. Here, we investigated the development of bNAbs in longitudinal plasma of HCV-infected persons with persistent infection or spontaneous clearance of multiple reinfections. By measuring plasma antibody neutralization of a heterologous virus panel, we found that the breadth and potency of the antibody response increased upon exposure to multiple genetically distinct infections and with longer duration of viremia. Greater genetic divergence between infecting strains was not associated with enhanced neutralizing breadth. Rather, repeated exposure to antigenically related, antibody-sensitive E1E2s was associated with potent bNAb induction. These data reveal that a prime-boost vaccine strategy with genetically distinct, antibody-sensitive viruses is a promising approach to inducing potent bNAbs in humans.

Indexed as

HepacivirusHepatitis CAntibodies, NeutralizingBroadly Neutralizing AntibodiesHepatitis C AntibodiesHumansViral Envelope ProteinsViremiaAntibodies, NeutralizingBroadly Neutralizing AntibodiesHepatitis C AntibodiesViral Envelope ProteinsAdaptive immunityAntigenHepatitisImmunologyVirology

Identifiers

PMID35588376
PMCPMC9337827
OpenAlexW4280600709

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.