Evidence map›Paper›PMID 34707161›Full record

ArticleNature communications2021

A Newcastle disease virus expressing a stabilized spike protein of SARS-CoV-2 induces protective immune responses.

Weina Sun, Yonghong Liu, Fatima Amanat, Irene González-Domínguez, Stephen McCroskery, Stefan Slamanig, Lynda Coughlan, Victoria Rosado, Nicholas Lemus, Sonia Jangra and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
6.2field-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

70 citing papers in PubMed, 117 citations in OpenAlex.

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  6. Stabilized mosaic hemagglutinin immunogens as novel universal influenza virus vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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10 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

25 authors at 6 institutions in 4 countries.

Weina SunDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0002-2435-5047
Yonghong LiuDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Fatima AmanatDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0002-8029-8227
Irene González-DomínguezDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0002-7920-5505
Stephen McCroskeryDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Stefan SlamanigDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0003-3694-6597
Lynda CoughlanUniversity of Maryland School of Medicine, Department of Microbiology and Immunology, Baltimore, MD, 21201, USA.ORCID 0000-0001-9880-6560
Victoria RosadoDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Nicholas LemusDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Sonia JangraDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Raveen RathnasingheDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Michael SchotsaertDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0003-3156-3132
Jose L MartinezDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Kaori SanoDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Ignacio MenaDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0001-5464-7086
Bruce L InnisPATH, Center for Vaccine Access and Innovation, Washington, DC, 20001, USA.ORCID 0000-0002-1753-7248
Ponthip WirachwongThe Government Pharmaceutical Organization, Bangkok, 10400, Thailand.
Duong Huu ThaiInstitute of Vaccines and Medical Biologicals, Nha Trang City, Khanh Hoa Province, Vietnam.
Ricardo Das Neves OliveiraInstituto Butantan, São Paulo, SP, 05503-900, Brazil.
Rami ScharfPATH, Center for Vaccine Access and Innovation, Washington, DC, 20001, USA.
Richard HjorthPATH, Center for Vaccine Access and Innovation, Washington, DC, 20001, USA.
Rama RaghunandanPATH, Center for Vaccine Access and Innovation, Washington, DC, 20001, USA.
Florian KrammerDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0003-4121-776X
Adolfo García-SastreDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0002-6551-1827
Peter PaleseDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. peter.palese@mssm.edu.ORCID 0000-0002-0337-5823
Icahn School of Medicine at Mount Sinai · USProgram for Appropriate Technology in Health · USGovernment of Thailand · THInstitute of Vaccine and Medical Biologicals · VNInstituto Butantan · BRUniversity of Maryland, Baltimore · US

Funding

NIAID NIH HHS HHSN272201400008C
6 · The paper itself

Abstract

Rapid development of COVID-19 vaccines has helped mitigating SARS-CoV-2 spread, but more equitable allocation of vaccines is necessary to limit the global impact of the COVID-19 pandemic and the emergence of additional variants of concern. We have developed a COVID-19 vaccine candidate based on Newcastle disease virus (NDV) that can be manufactured at high yields in embryonated eggs. Here, we show that the NDV vector expressing an optimized spike antigen (NDV-HXP-S) is a versatile vaccine inducing protective antibody responses. NDV-HXP-S can be administered intramuscularly as inactivated vaccine or intranasally as live vaccine. We show that NDV-HXP-S GMP-produced in Vietnam, Thailand and Brazil is effective in the hamster model. Furthermore, we show that intramuscular vaccination with NDV-HXP-S reduces replication of tested variants of concerns in mice. The immunity conferred by NDV-HXP-S effectively counteracts SARS-CoV-2 infection in mice and hamsters.

Indexed as

AnimalsFemaleMiceMice, Inbred BALB CNewcastle disease virusSARS-CoV-2Spike Glycoprotein, CoronavirusVaccines, AttenuatedSpike Glycoprotein, CoronavirusVaccines, Attenuated

Identifiers

PMID34707161
PMCPMC8551302
OpenAlexW3208797239

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.