Evidence map›Paper›PMID 29949635›Full record

ArticlePloS one2018

Development of a high-throughput assay to detect antibody inhibition of low pH induced conformational changes of influenza virus hemagglutinin.

Jessica F Trost, Elizabeth H LeMasters, Feng Liu, Paul Carney, Xiuhua Lu, Kanetsu Sugawara, Seiji Hongo, James Stevens, David A Steinhauer, Terrence Tumpey and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Influenza Virus Entry inhibitors.Advances in experimental medicine and biology · 2022
    Review
  2. Article
  3. Article
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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

13 authors at 3 institutions in 2 countries.

Jessica F TrostInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Elizabeth H LeMastersInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Feng LiuInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Paul CarneyInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Xiuhua LuInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Kanetsu SugawaraDepartment of Infectious Diseases, Yamagata University Faculty of Medicine, Yamagata, Japan.
Seiji HongoDepartment of Infectious Diseases, Yamagata University Faculty of Medicine, Yamagata, Japan.
James StevensInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
David A SteinhauerDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Terrence TumpeyInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Jacqueline M KatzInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Min Z LevineInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Zhu-Nan LiInfluenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID 0000-0002-4556-8551
Centers for Disease Control and Prevention · USYamagata University · JPEmory University · US

Funding

Antimicrobial Resistance and Therapeutic Discovery Training ProgramT32AI106699 · NIAID · EMORY UNIVERSITY · PI Graeme L Conn, Joanna B Goldberg · 2014 to 2026
$2.7M
NIAID NIH HHS HHSN272201400004CNIAID NIH HHS T32 AI106699
6 · The paper itself

Abstract

Many broadly neutralizing antibodies (bnAbs) bind to conserved areas of the hemagglutinin (HA) stalk region and can inhibit the low pH induced HA conformational changes necessary for viral membrane fusion activity. We developed and evaluated a high-throughput virus-free and cell-free ELISA based low pH induced HA Conformational Change Inhibition Antibody Detection Assay (HCCIA) and a complementary proteinase susceptibility assay. Human serum samples (n = 150) were tested by HCCIA using H3 recombinant HA. Optical density (OD) ratios of mAb HC31 at pH 4.8 to pH 7.0 ranged from 0.87 to 0.09. Our results demonstrated that low pH induced HA conformational change inhibition antibodies (CCI) neutralized multiple H3 strains after removal of head-binding antibodies. The results suggest that HCCIA can be utilized to detect and characterize CCI in sera, that are potentially broadly neutralizing, and serves as a useful tool for evaluating universal vaccine candidates targeting the HA stalk.

Indexed as

Antibodies, NeutralizingEnzyme-Linked Immunosorbent AssayHemagglutinin Glycoproteins, Influenza VirusHigh-Throughput Screening AssaysHumansHydrogen-Ion ConcentrationInfluenza A Virus, H3N2 SubtypeInfluenza, HumanModels, MolecularProtein ConformationRecombinant ProteinsAntibodies, NeutralizingHemagglutinin Glycoproteins, Influenza VirusRecombinant Proteins

Identifiers

PMID29949635
PMCPMC6021090
OpenAlexW2810383866

What OpenQuestion holds

Textmetadata
LicenceCC0
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.