Evidence map›Paper›PMID 35482816›Full record

ArticlePLoS pathogens2022

A combination of potently neutralizing monoclonal antibodies isolated from an Indian convalescent donor protects against the SARS-CoV-2 Delta variant.

Nitin Hingankar, Suprit Deshpande, Payel Das, Zaigham Abbas Rizvi, Constantinos Kurt Wibmer, Poppy Mashilo, Mohammed Yousuf Ansari, Alison Burns, Shawn Barman, Fangzhu Zhao and 24 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 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 19% 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.

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  6. Pharmacological potential ofFrontiers in immunology · 2023
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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

34 authors at 4 institutions in 3 countries.

Nitin HingankarIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Suprit DeshpandeIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Payel DasIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Zaigham Abbas RizviImmuno-biology Lab, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Constantinos Kurt WibmerNational Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS), Johannesburg, South Africa.
Poppy MashiloNational Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS), Johannesburg, South Africa.
Mohammed Yousuf AnsariIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Alison BurnsScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Shawn BarmanScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Fangzhu ZhaoScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Sohini MukherjeeIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Jonathan L TorresScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Souvick ChattopadhyayTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Farha MehdiTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Jyoti SutarIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Deepak Kumar RathoreImmunology Core, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Kamal PargaiBioassay laboratory, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Janmejay SinghBioassay laboratory, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Sudipta SonarTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Kamini JakharTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Jyotsna DandotiyaImmuno-biology Lab, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Sankar BhattacharyyaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Shailendra ManiTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Sweety SamalTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Savita SinghTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Pallavi KshetrapalTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Ramachandran ThiruvengadamTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Gaurav BatraTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Guruprasad MedigeshiTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Andrew B WardScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Shinjini BhatnagarTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Amit AwasthiImmuno-biology Lab, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Devin SokScripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
Jayanta BhattacharyaIAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.ORCID 0000-0002-1531-3822
Translational Health Science and Technology Institute · INScripps Research Institute · USInternational AIDS Vaccine Initiative · USNational Health Laboratory Service · ZA

Funding

Rational structure-guided design of broadly reactive next-generation therapeutics to treat non-communicable snakebite in AfricaR21TW011454 · FIC · WITS HEALTH CONSORTIUM (PTY), LTD · PI WIBMER, CONSTANTINOS KURT · 2019 to 2021
$373k
FIC NIH HHS R21 TW011454
6 · The paper itself

Abstract

Although efficacious vaccines have significantly reduced the morbidity and mortality of COVID-19, there remains an unmet medical need for treatment options, which monoclonal antibodies (mAbs) can potentially fill. This unmet need is exacerbated by the emergence and spread of SARS-CoV-2 variants of concern (VOCs) that have shown some resistance to vaccine responses. Here we report the isolation of five neutralizing mAbs from an Indian convalescent donor, out of which two (THSC20.HVTR04 and THSC20.HVTR26) showed potent neutralization of SARS-CoV-2 VOCs at picomolar concentrations, including the Delta variant (B.1.617.2). One of these (THSC20.HVTR26) also retained activity against the Omicron variant. These two mAbs target non-overlapping epitopes on the receptor-binding domain (RBD) of the spike protein and prevent virus attachment to its host receptor, human angiotensin converting enzyme-2 (hACE2). Furthermore, the mAb cocktail demonstrated protection against the Delta variant at low antibody doses when passively administered in the K18 hACE2 transgenic mice model, highlighting their potential as a cocktail for prophylactic and therapeutic applications. Developing the capacity to rapidly discover and develop mAbs effective against highly transmissible pathogens like coronaviruses at a local level, especially in a low- and middle-income country (LMIC) such as India, will enable prompt responses to future pandemics as an important component of global pandemic preparedness.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralMiceSpike Glycoprotein, CoronavirusAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID35482816
PMCPMC9089897
OpenAlexW4226049994

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.