Evidence map›Paper›PMID 36366469›Full record

ArticleViruses2022

Feasibility of Polyclonal Avian Immunoglobulins (IgY) as Prophylaxis against Human Norovirus Infection.

Chad Artman, Nnebuefe Idegwu, Kyle D Brumfield, Ken Lai, Shirley Hauta, Darryl Falzarano, Viviana Parreño, Lijuan Yuan, James D Geyer, Julius G Goepp

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Latest Findings in Immunoglobulin Y Technologies and Applications.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. Review
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

10 authors at 4 institutions in 3 countries.

Chad ArtmanScaled Microbiomics, LLC, Hagerstown, MD 21740, USA.
Nnebuefe IdegwuScaled Microbiomics, LLC, Hagerstown, MD 21740, USA.ORCID 0000-0002-0019-5210
Kyle D BrumfieldMaryland Pathogen Research Institute, University of Maryland, College Park Campus, College Park, MD 20742, USA.ORCID 0000-0002-3234-3337
Ken LaiVaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, SK S7N 5E3, Canada.
Shirley HautaVaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, SK S7N 5E3, Canada.
Darryl FalzaranoVaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, SK S7N 5E3, Canada.ORCID 0000-0002-8805-8068
Viviana ParreñoDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Lijuan YuanDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.ORCID 0000-0003-0709-5228
James D GeyerInstitute for Rural Health Research, College of Community Health Science, University of Alabama, Tuscaloosa, AL 35487, USA.ORCID 0000-0002-2776-1737
Julius G GoeppScaled Microbiomics, LLC, Hagerstown, MD 21740, USA.ORCID 0000-0001-9449-968X
University of Saskatchewan · CAVirginia–Maryland College of Veterinary Medicine · USUniversity of Alabama · USUniversity of Maryland, College Park · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman norovirus (HuNoV) is the leading viral cause of diarrhea, with GII.4 as the predominant genotype of HuNoV outbreaks globally. However, new genogroup variants emerge periodically, complicating the development of anti-HuNoV vaccines; other prophylactic or therapeutic medications specifically for HuNoV disease are lacking. Passive immunization using oral anti-HuNoV antibodies may be a rational alternative. Here, we explore the feasibility of using avian immunoglobulins (IgY) for preventing HuNoV infection in vitro in a human intestinal enteroid (HIE) model.

methodsHens were immunized with virus-like particles (VLP) of a GII.4 HuNoV strain (GII.4/CHDC2094/1974/US) by intramuscular injection. The resulting IgY was evaluated for inhibition of binding to histo-blood group antigens (HBGA) and viral neutralization against representative GII.4 and GII.6 clinical isolates, using an HIE model.

resultsIgY titers were detected by three weeks following initial immunization, persisting at levels of 1:2

conclusionsWe demonstrate the feasibility of IgY for preventing infection of HIE by HuNoV GII.4. Clinical preparations should cover multiple circulating HuNoV genotypes for comprehensive effects. Plans for animal studies are underway.

Indexed as

Blood Group AntigensCaliciviridae InfectionsNorovirusAnimalsAntibodiesChickensFeasibility StudiesFemaleHumansImmunoglobulinsAntibodiesBlood Group AntigensIgYImmunoglobulinscalicivirusfoodborne diseasegastroenteritis outbreaksIgYnorovirusoutbreak prevention and controlpassive immunotherapy

Identifiers

PMID36366469
PMCPMC9698945
OpenAlexW4307436718

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.