Evidence map›Paper›PMID 34161386›Full record

ArticlePloS one2021

The Fc-mediated effector functions of a potent SARS-CoV-2 neutralizing antibody, SC31, isolated from an early convalescent COVID-19 patient, are essential for the optimal therapeutic efficacy of the antibody.

Conrad E Z Chan, Shirley G K Seah, De Hoe Chye, Shane Massey, Maricela Torres, Angeline P C Lim, Steven K K Wong, Jacklyn J Y Neo, Pui San Wong, Jie Hui Lim and 20 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
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  8. Antibody-dependent enhancement of coronaviruses.International journal of biological sciences · 2025
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12 more citing papers are in PubMed but not listed here.

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 2 countries.

Conrad E Z ChanBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Shirley G K SeahBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
De Hoe ChyeBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Shane MasseyDepartment of Microbiology & Immunology and Office of Regulated Nonclinical Studies, University of Texas Medical Branch, Galveston, TX, United States of America.
Maricela TorresDepartment of Microbiology & Immunology and Office of Regulated Nonclinical Studies, University of Texas Medical Branch, Galveston, TX, United States of America.
Angeline P C LimBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Steven K K WongBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Jacklyn J Y NeoBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Pui San WongBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Jie Hui LimBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Gary S L LohBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Dongling WangBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.
Jerome D Boyd-KirkupHummingbird Bioscience, Singapore, Singapore.
Siyu GuanHummingbird Bioscience, Singapore, Singapore.
Dipti ThakkarHummingbird Bioscience, Singapore, Singapore.
Guo Hui TeoLife Science Institute, National University of Singapore, Singapore, Singapore.
Kiren PurushotormanLife Science Institute, National University of Singapore, Singapore, Singapore.
Paul E HutchinsonLife Science Institute, National University of Singapore, Singapore, Singapore.
Barnaby E YoungNational Centre for Infectious Diseases, Singapore, Singapore.
Jenny G LowSingapore General Hospital, Singapore, Singapore.
Paul A MacAryDepartment of Microbiology & Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Hannes HentzeExperimental Drug Development Centre, Therapeutics Development, A*STAR Research Entities (ARES), Singapore, Singapore.
Venkateshan S PrativadibhayankaraExperimental Drug Development Centre, Therapeutics Development, A*STAR Research Entities (ARES), Singapore, Singapore.
Kantharaj EthirajuluExperimental Drug Development Centre, Therapeutics Development, A*STAR Research Entities (ARES), Singapore, Singapore.
Jason E ComerDepartment of Microbiology & Immunology and Office of Regulated Nonclinical Studies, University of Texas Medical Branch, Galveston, TX, United States of America.
Chien-Te K TsengDepartment of Microbiology & Immunology and Center of Biodefense and Emerging Disease, University of Texas Medical Branch, Galveston, TX, United States of America.
Alan D T BarrettDepartment of Pathology and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston, TX, United States of America.
Piers J IngramHummingbird Bioscience, Singapore, Singapore.
Trevor BraselDepartment of Microbiology & Immunology and Office of Regulated Nonclinical Studies, University of Texas Medical Branch, Galveston, TX, United States of America.
Brendon John HansonBiological Defence Programme, DSO National Laboratories, Singapore, Singapore.ORCID 0000-0001-8752-2650
DSO National Laboratories · SGThe University of Texas Medical Branch at Galveston · USNational University of Singapore · SGExperimental Drug Development Centre · SGNational Centre for Infectious Diseases · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although SARS-CoV-2-neutralizing antibodies are promising therapeutics against COVID-19, little is known about their mechanism(s) of action or effective dosing windows. We report the generation and development of SC31, a potent SARS-CoV-2 neutralizing antibody, isolated from a convalescent patient. Antibody-mediated neutralization occurs via an epitope within the receptor-binding domain of the SARS-CoV-2 Spike protein. SC31 exhibited potent anti-SARS-CoV-2 activities in multiple animal models. In SARS-CoV-2 infected K18-human ACE2 transgenic mice, treatment with SC31 greatly reduced viral loads and attenuated pro-inflammatory responses linked to the severity of COVID-19. Importantly, a comparison of the efficacies of SC31 and its Fc-null LALA variant revealed that the optimal therapeutic efficacy of SC31 requires Fc-mediated effector functions that promote IFNγ-driven anti-viral immune responses, in addition to its neutralization ability. A dose-dependent efficacy of SC31 was observed down to 5mg/kg when administered before viral-induced lung inflammatory responses. In addition, antibody-dependent enhancement was not observed even when infected mice were treated with SC31 at sub-therapeutic doses. In SARS-CoV-2-infected hamsters, SC31 treatment significantly prevented weight loss, reduced viral loads, and attenuated the histopathology of the lungs. In rhesus macaques, the therapeutic potential of SC31 was evidenced through the reduction of viral loads in both upper and lower respiratory tracts to undetectable levels. Together, the results of our preclinical studies demonstrated the therapeutic efficacy of SC31 in three different models and its potential as a COVID-19 therapeutic candidate.

Indexed as

Angiotensin-Converting Enzyme 2AnimalsAntibodies, NeutralizingChemokinesChlorocebus aethiopsConvalescenceCOVID-19CricetinaeCytokinesDisease Models, AnimalDose-Response Relationship, DrugFemaleHumansImmunoglobulin Fc FragmentsImmunoglobulin GMacaca mulattaACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingChemokinesCytokinesImmunoglobulin Fc FragmentsImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID34161386
PMCPMC8221499
OpenAlexW3177362856

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.