Evidence map›Paper›PMID 36359294›Full record

ArticleBiomedicines2022

Immunoglobulin Y Specific for SARS-CoV-2 Spike Protein Subunits Effectively Neutralizes SARS-CoV-2 Infectivity and Ameliorates Disease Manifestations In Vivo.

Chia-Tsui Yeh, Chia-Ying Lee, Yi-Jung Ho, Sin-An Chen, Liang-Yu Chen, Ping-Cheng Liu, Yuan-Fan Chin, An-Yu Chen, Po-Shiuan Hsieh, Yi-Jen Hung and 3 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

13 authors at 2 institutions in 1 country.

Chia-Tsui YehSchool of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Chia-Ying LeeInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
Yi-Jung HoSchool of Pharmacy and Graduate Institute of Pharmacy, National Defense Medical Center, Taipei 114, Taiwan.
Sin-An ChenInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
Liang-Yu ChenInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
Ping-Cheng LiuInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.ORCID 0000-0003-2576-4309
Yuan-Fan ChinInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
An-Yu ChenInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
Po-Shiuan HsiehGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0002-3402-9851
Yi-Jen HungInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.
Cheng-Cheung ChenInstitute of Preventive Medicine, National Defense Medical Center, New Taipei 237, Taiwan.ORCID 0000-0002-7002-8426
Yu-Chie WangSchool of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Guan-Chiun LeeSchool of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
National Defense Medical Center · TWNational Taiwan Normal University · TW

Funding

Ministry of Science and Technology MOST 111-2321-B-016-002
6 · The paper itself

Abstract

(Background) The coronavirus disease 2019 (COVID-19) that is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) carries high infectivity and mortality. Efficient intervention strategies are urgently needed. Avian immunoglobulin Y (IgY) showed efficacy against viral infection whereas the in vivo efficacy remains unclear. (Methods) We immunized laying hens with S1, S1 receptor-binding domain (S1-RBD), or S2 subunits of the SARS-CoV-2 spike (S) protein. After immunization, IgYs were collected and extracted from the egg yolks. The neutralization potential of IgYs was examined by the plaque reduction neutralization test (PRNT). The bioutility of IgYs was examined in Syrian hamsters in vivo. (Results) IgYs exhibited typical banding patterns in SDS-PAGE and Western blot and were immunoreactive against S1, S1-RBD, and S2 subunits. The plaque reduction neutralization test (PRNT) showed that all purified IgYs potently neutralized different SARS-CoV-2 strains in vitro. In Syrian hamsters, the combination of IgYs for S1-RBD and S2 subunits administered before or after SARS-CoV-2 infection effectively restored body weight loss and reduced intrapulmonary lesions and the amount of immunoreactive N protein-positive cells, which were caused by SARS-CoV-2 infection. (Conclusions) Collectively, IgYs specific for S protein subunits effectively neutralized SARS-CoV-2 in vitro and in vivo and may serve as prophylactic or therapeutic antibodies in the prevention or treatment of COVID-19.

Indexed as

immunoglobulin yreceptor-binding domainsevere acute respiratory syndrome coronavirus 2spike proteinyolk

Identifiers

PMID36359294
PMCPMC9687769
OpenAlexW4307921986

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.