Evidence map›Paper›PMID 34673836›Full record

ArticlePLoS pathogens2021

Structure-guided antibody cocktail for prevention and treatment of COVID-19.

Shih-Chieh Su, Tzu-Jing Yang, Pei-Yu Yu, Kang-Hao Liang, Wan-Yu Chen, Chun-Wei Yang, Hsiu-Ting Lin, Mei-Jung Wang, Ruei-Min Lu, Hsien-Cheng Tso and 20 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  7. Current clinical status of new COVID-19 vaccines and immunotherapy.Environmental science and pollution research international · 2022
    Review
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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

30 authors at 5 institutions in 1 country.

Shih-Chieh SuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Tzu-Jing YangInstitute of Biologic Chemistry, Academia Sinica, Taipei, Taiwan.
Pei-Yu YuInstitute of Biologic Chemistry, Academia Sinica, Taipei, Taiwan.
Kang-Hao LiangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Wan-Yu ChenInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Chun-Wei YangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Hsiu-Ting LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Mei-Jung WangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Ruei-Min LuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Hsien-Cheng TsoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Meng-Jhe ChungInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Tzung-Yang HsiehInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Yu-Ling ChangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Shin-Chang LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Fang-Yu HsuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Feng-Yi KeInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Yi-Hsuan WuInstitute of Biologic Chemistry, Academia Sinica, Taipei, Taiwan.
Yu-Chyi HwangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
I-Ju LiuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Jian-Jong LiangBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Chun-Che LiaoBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Hui-Ying KoBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Cheng-Pu SunBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Ping-Yi WuBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Jia-Tsrong JanGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Yuan-Chih ChangInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-0289-3768
Yi-Ling LinBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Mi-Hua TaoBiomedical Translation Research Center (BioTReC), Academia Sinica, Taipei, Taiwan.
Shang-Te Danny HsuInstitute of Biologic Chemistry, Academia Sinica, Taipei, Taiwan.
Han-Chung WuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-5185-1169
Institute of Biomedical Sciences, Academia Sinica · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TWInstitute of Biological Chemistry, Academia Sinica · TWNational Taiwan University · TWGenomics Research Center, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of effective therapeutics for mitigating the COVID-19 pandemic is a pressing global need. Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. With the emergence of more contagious variants of SARS-CoV-2, cocktail antibody therapies hold great promise to control disease and prevent drug resistance.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCOVID-19CricetinaeDisease Models, AnimalFemaleMaleMiceSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID34673836
PMCPMC8530329
OpenAlexW3205165947

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.