Evidence map›Paper›PMID 35895717›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

A highly efficacious live attenuated mumps virus-based SARS-CoV-2 vaccine candidate expressing a six-proline stabilized prefusion spike.

Yuexiu Zhang, Mijia Lu, K C Mahesh, Eunsoo Kim, Mohamed M Shamseldin, Chengjin Ye, Piyush Dravid, Michelle Chamblee, Jun-Gyu Park, Jesse M Hall and 13 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

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  14. Bacterial Artificial Chromosome Reverse Genetics Approaches for SARS-CoV-2.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  15. A next-generation intranasal trivalent MMS vaccine induces durable and broad protection against SARS-CoV-2 variants of concern.Proceedings of the National Academy of Sciences of the United States of America · 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

23 authors at 3 institutions in 1 country.

Yuexiu ZhangDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.
Mijia LuDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.
K C MaheshCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0002-5177-9566
Eunsoo KimDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.ORCID 0000-0003-4196-8280
Mohamed M ShamseldinDepartment of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH 43210.
Chengjin YeDepartment of Disease Intervention and Prevention, Texas Biomedical Research Institute, San Antonio, TX 78227.ORCID 0000-0002-1934-9494
Piyush DravidCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0002-4790-9591
Michelle ChambleeDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.
Jun-Gyu ParkDepartment of Disease Intervention and Prevention, Texas Biomedical Research Institute, San Antonio, TX 78227.ORCID 0000-0001-7163-3591
Jesse M HallDepartment of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH 43210.
Sheetal TrivediCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.
Supranee ChaiwatpongsakornCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0003-3511-7359
Adam D KennyDepartment of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH 43210.
Satyapramod Srinivasa MurthyCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.
Himanshu SharmaCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0003-1679-1591
Xueya LiangDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.
Jacob S YountDepartment of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH 43210.
Amit KapoorCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0002-8117-7347
Luis Martinez-SobridoDepartment of Disease Intervention and Prevention, Texas Biomedical Research Institute, San Antonio, TX 78227.ORCID 0000-0001-7084-0804
Purnima DubeyDepartment of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH 43210.ORCID 0000-0002-5454-8421
Prosper N BoyakaDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.ORCID 0000-0001-6857-9088
Mark E PeeplesCenter for Vaccines and Immunity, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205.ORCID 0000-0002-4582-317X
Jianrong LiDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210.
The Ohio State University · USNationwide Children's Hospital · USTexas Biomedical Research Institute · US

Funding

Transcriptome-wide base-resolution sequencing of pseudouridine in human normal and AD brain tissues-CEGS Admin supplement 2020-2021RM1HG008935 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, CHUAN · 2016 to 2025
$24.4M
Technology Development Project - Increasing the complexity of ex vivo human airway models for studying immune response to viral infectionU19AI142733 · NIAID · JACKSON LABORATORY · PI Anna Karolina Palucka · 2019 to 2026
$23.1M
Project 3: Dr. LiP01AI112524 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI LI, JIANRONG · 2015 to 2019
$6.8M
Mechanisms of innate resistance to virus infectionsR01AI130110 · NIAID · OHIO STATE UNIVERSITY · PI Jacob Yount · 2017 to 2026
$4.3M
Messenger RNA Capping and Methylation in PneumovirusesR01AI090060 · NIAID · OHIO STATE UNIVERSITY · PI LI, JIANRONG · 2011 to 2023
$4.0M
Host Responses to the Pore-Forming Toxin Listeriolysin OR01AI157205 · NIAID · OHIO STATE UNIVERSITY · PI AMER, AMAL O, BOYAKA, PROSPER N · 2021 to 2025
$3.2M
Targeting myeloid cells for regulation of alum-based immunityR01AI145144 · NIAID · OHIO STATE UNIVERSITY · PI BOYAKA, PROSPER N · 2020 to 2024
$3.1M
Host response and liver disease in a hepatitis C-like virus rat modelR01AI137567 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI KAPOOR, AMIT · 2018 to 2022
$2.5M
Immune correlates of protection against hepacivirus persistence.R01AI151175 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI KAPOOR, AMIT · 2021 to 2024
$2.5M
Establishing a relevant mouse model with susceptibility to non-adapted influenza viruses for vaccine challenge studiesR21AI151230 · NIAID · OHIO STATE UNIVERSITY · PI YOUNT, JACOB · 2020 to 2021
$409k
NHGRI NIH HHS RM1 HG008935NIAID NIH HHS P01 AI112524NIAID NIH HHS R01 AI090060NIAID NIH HHS R01 AI130110NIAID NIH HHS R01 AI137567NIAID NIH HHS R01 AI145144NIAID NIH HHS R01 AI151175NIAID NIH HHS R01 AI157205NIAID NIH HHS R21 AI151230NIAID NIH HHS U19 AI142733
6 · The paper itself

Abstract

With the rapid increase in SARS-CoV-2 cases in children, a safe and effective vaccine for this population is urgently needed. The MMR (measles/mumps/rubella) vaccine has been one of the safest and most effective human vaccines used in infants and children since the 1960s. Here, we developed live attenuated recombinant mumps virus (rMuV)-based SARS-CoV-2 vaccine candidates using the MuV Jeryl Lynn (JL2) vaccine strain backbone. The soluble prefusion SARS-CoV-2 spike protein (preS) gene, stablized by two prolines (preS-2P) or six prolines (preS-6P), was inserted into the MuV genome at the P-M or F-SH gene junctions in the MuV genome. preS-6P was more efficiently expressed than preS-2P, and preS-6P expression from the P-M gene junction was more efficient than from the F-SH gene junction. In mice, the rMuV-preS-6P vaccine was more immunogenic than the rMuV-preS-2P vaccine, eliciting stronger neutralizing antibodies and mucosal immunity. Sera raised in response to the rMuV-preS-6P vaccine neutralized SARS-CoV-2 variants of concern, including the Delta variant equivalently. Intranasal and/or subcutaneous immunization of IFNAR1

Indexed as

COVID-19COVID-19 VaccinesMeasles-Mumps-Rubella VaccineSARS-CoV-2Spike Glycoprotein, CoronavirusVaccine EfficacyAnimalsAntibodies, NeutralizingAntibodies, ViralImmunogenicity, VaccineMesocricetusMiceMumps virusProlineVaccines, AttenuatedAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesMeasles-Mumps-Rubella VaccineProlineSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, Attenuatedmumps virusSARS-CoV-2vaccine

Identifiers

PMID35895717
PMCPMC9388148
OpenAlexW4288067653

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.