Evidence map›Paper›PMID 37855638›Full record

ArticleJournal of virology2023

Discovery of Nanosota-2, -3, and -4 as super potent and broad-spectrum therapeutic nanobody candidates against COVID-19.

Gang Ye, Ruangang Pan, Fan Bu, Jian Zheng, Alise Mendoza, Wei Wen, Lanying Du, Benjamin Spiller, Brian E Wadzinski, Bin Liu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Nanobodies targeting SARS-CoV-2 variants.Acta pharmaceutica Sinica. B · 2026
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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

12 authors at 4 institutions in 1 country.

Gang Ye *Department of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.
Ruangang Pan *Department of Microbiology and Immunology, University of Iowa , Iowa City, Iowa, USA.
Fan Bu *Department of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.
Jian ZhengDepartment of Microbiology and Immunology, University of Iowa , Iowa City, Iowa, USA.
Alise MendozaDepartment of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.
Wei WenDepartment of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.
Lanying DuInstitute for Biomedical Sciences, Georgia State University , Atlanta, Georgia, USA.ORCID 0000-0001-5955-1294
Benjamin SpillerDepartment of Pharmacology, Vanderbilt University School of Medicine , Nashville, Tennessee, USA.
Brian E WadzinskiDepartment of Pharmacology, Vanderbilt University School of Medicine , Nashville, Tennessee, USA.
Bin LiuHormel Institute, University of Minnesota , Austin, Minnesota, USA.ORCID 0000-0002-6581-780X
Stanley PerlmanDepartment of Microbiology and Immunology, University of Iowa , Iowa City, Iowa, USA.ORCID 0000-0003-4213-2354
Fang LiDepartment of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.ORCID 0000-0002-1958-366X
University of Minnesota · USUniversity of Iowa · USVanderbilt University · USGeorgia State University · US

Funding

Project 5: Pandemic Virus Helicase InhibitorsU19AI171954 · NIAID · UNIVERSITY OF MINNESOTA · PI Donghoon Chung · 2022 to 2026
$100.9M
Receptor recognition mechanisms of coronavirusesR01AI089728 · NIAID · UNIVERSITY OF MINNESOTA · PI Fang Li, Timothy Patrick Sheahan · 2010 to 2026
$4.7M
Novel nanobodies to prevent and treat SARS-CoV-2 and other pathogenic human coronavirusesR01AI157975 · NIAID · NEW YORK BLOOD CENTER · PI DU, LANYING, LI, FANG · 2020 to 2025
$3.9M
NIAID NIH HHS R01 AI089728NIAID NIH HHS R01 AI157975NIAID NIH HHS U19 AI171954
6 · The paper itself

Abstract

importanceThe COVID-19 pandemic exposed limitations of conventional antibodies as therapeutics, including high cost, limited potency, ineffectiveness against new viral variants, and primary reliance on injection-only delivery. Nanobodies are single-domain antibodies with therapeutic potentials. We discovered three anti-SARS-CoV-2 nanobodies, named Nanosota-2, -3, and -4, from an immunized alpaca. Nanosota-2 is super potent against prototypic SARS-CoV-2, Nanosota-3 is highly potent against the omicron variant, and Nanosota-4 is effective against both SARS-CoV-1 and SARS-CoV-2. In addition to their super potency and combined broad antiviral spectrum, these nanobodies are cost-effective, can be easily adapted to new viral variants through phage display, and can potentially be administered as inhalers. The Nanosota series are powerful therapeutic candidates to combat circulating SARS-CoV-2 and prepare for possible future coronavirus pandemics.

Indexed as

COVID-19SARS-CoV-2Single-Domain AntibodiesAntibodies, NeutralizingAntibodies, ViralHumansPandemicsSpike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralSingle-Domain AntibodiesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ACE2animal modelcryo-EMomicronreceptor-binding domainSARS-CoV-1SARS-CoV-2single-domain antibody from camelidsspike proteinvirus neutralization

Identifiers

PMID37855638
PMCPMC10688364
OpenAlexW4387765109

What OpenQuestion holds

Textmetadata
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.