Evidence map›Paper›PMID 36114224›Full record

ArticleScientific reports2022

Reevaluation of antibody-dependent enhancement of infection in anti-SARS-CoV-2 therapeutic antibodies and mRNA-vaccine antisera using FcR- and ACE2-positive cells.

Jun Shimizu, Tadahiro Sasaki, Ritsuko Koketsu, Ryo Morita, Yuka Yoshimura, Ami Murakami, Yua Saito, Toshie Kusunoki, Yoshihiro Samune, Emi E Nakayama and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
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  3. Review
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  13. IFN-γ derived from activated human CD4Scientific reports · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Jun ShimizuMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan.
Tadahiro SasakiDepartment of Viral Infections, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Ritsuko KoketsuDepartment of Viral Infections, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Ryo MoritaOsaka City Juso Hospital, 2-12-27, Nonakakita, Yodogawa-ku, Osaka, 532-0034, Japan.
Yuka YoshimuraMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan.
Ami MurakamiMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan.
Yua SaitoMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan.
Toshie KusunokiMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan.
Yoshihiro SamuneDepartment of Viral Infections, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Emi E NakayamaDepartment of Viral Infections, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Kazuo MiyazakiMiCAN Technologies Inc, KKVP 1-36, Goryo-ohara, Nishikyo-Ku, Kyoto, 615-8245, Japan. kmiyazaki@micantechnologies.com.
Tatsuo ShiodaDepartment of Viral Infections, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita, Osaka, 565-0871, Japan. shioda@biken.osaka-u.ac.jp.
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many therapeutic antibodies (Abs) and mRNA vaccines, both targeting SARS-CoV-2 spike protein (S-protein), have been developed and approved in order to combat the ongoing COVID-19 pandemic. In consideration of these developments, a common concern has been the potential for Ab-dependent enhancement (ADE) of infection caused by inoculated or induced Abs. Although the preventive and therapeutic effects of these Abs are obvious, little attention has been paid to the influence of the remaining and dwindling anti-S-protein Abs in vivo. Here, we demonstrate that certain monoclonal Abs (mAbs) approved as therapeutic neutralizing anti-S-protein mAbs for human usage have the potential to cause ADE in a narrow range of Ab concentrations. Although sera collected from mRNA-vaccinated individuals exhibited neutralizing activity, some sera gradually exhibited dominance of ADE activity in a time-dependent manner. None of the sera examined exhibited neutralizing activity against infection with the Omicron strain. Rather, some ADE of Omicron infection was observed in some sera. These results suggest the possible emergence of adverse effects caused by these Abs in addition to the therapeutic or preventive effect.

Indexed as

Antibody-Dependent EnhancementCOVID-19COVID-19 VaccinesImmune SeraSARS-CoV-2Angiotensin-Converting Enzyme 2Antibodies, ViralCOVID-19 SerotherapyHumansImmunization, PassivePandemicsSpike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2Antibodies, ViralCOVID-19 VaccinesImmune SeraSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID36114224
PMCPMC9481526
OpenAlexW4296160968

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.