Evidence map›Paper›PMID 35906244›Full record

ArticleNPJ vaccines2022

Mucosal administration of a live attenuated recombinant COVID-19 vaccine protects nonhuman primates from SARS-CoV-2.

Mariana F Tioni, Robert Jordan, Angie Silva Pena, Aditya Garg, Danlu Wu, Shannon I Phan, Christopher M Weiss, Xing Cheng, Jack Greenhouse, Tatyana Orekov and 12 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.9field-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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Mucosal immunity and vaccine development.Signal transduction and targeted therapy · 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

22 authors at 6 institutions in 1 country.

Mariana F Tioni *Meissa Vaccines Inc, Redwood City, CA, USA. mariana.tioni@meissavaccines.com.ORCID http://orcid.org/0000-0002-7865-3023
Robert Jordan *Meissa Vaccines Inc, Redwood City, CA, USA.
Angie Silva PenaMeissa Vaccines Inc, Redwood City, CA, USA.
Aditya GargMeissa Vaccines Inc, Redwood City, CA, USA.ORCID http://orcid.org/0000-0002-6179-4110
Danlu WuMeissa Vaccines Inc, Redwood City, CA, USA.
Shannon I PhanMeissa Vaccines Inc, Redwood City, CA, USA.
Christopher M WeissMeissa Vaccines Inc, Redwood City, CA, USA.ORCID http://orcid.org/0000-0003-4704-9533
Xing ChengMeissa Vaccines Inc, Redwood City, CA, USA.
Jack GreenhouseBIOQUAL Inc, Rockville, MD, USA.
Tatyana OrekovBIOQUAL Inc, Rockville, MD, USA.
Daniel ValentinBIOQUAL Inc, Rockville, MD, USA.
Swagata KarBIOQUAL Inc, Rockville, MD, USA.
Laurent PessaintBIOQUAL Inc, Rockville, MD, USA.
Hanne AndersenBIOQUAL Inc, Rockville, MD, USA.ORCID http://orcid.org/0000-0003-1103-9608
Christopher C StobartDepartment of Biological Sciences, Butler University, Indianapolis, IN, USA.
Melissa H BloodworthDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, USA.
R Stokes PeeblesDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, USA.
Yang LiuDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.
Xuping XieDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0003-0918-016X
Pei-Yong ShiDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0001-5553-1616
Martin L MooreMeissa Vaccines Inc, Redwood City, CA, USA.
Roderick S TangMeissa Vaccines Inc, Redwood City, CA, USA.
Meissa Vaccines (United States) · USBioqual · USThe University of Texas Medical Branch at Galveston · USVanderbilt University · USButler University · USGates Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the COVID-19 global pandemic. SARS-CoV-2 is an enveloped RNA virus that relies on its trimeric surface glycoprotein spike for entry into host cells. Here we describe the COVID-19 vaccine candidate MV-014-212, a live, attenuated, recombinant human respiratory syncytial virus expressing a chimeric SARS-CoV-2 spike as the only viral envelope protein. MV-014-212 was attenuated and immunogenic in African green monkeys (AGMs). One mucosal administration of MV-014-212 in AGMs protected against SARS-CoV-2 challenge, reducing by more than 200-fold the peak shedding of SARS-CoV-2 in the nose. MV-014-212 elicited mucosal immunoglobulin A in the nose and neutralizing antibodies in serum that exhibited cross-neutralization against virus variants of concern Alpha, Beta, and Delta. Intranasally delivered, live attenuated vaccines such as MV-014-212 entail low-cost manufacturing suitable for global deployment. MV-014-212 is currently in Phase 1 clinical trials as an intranasal COVID-19 vaccine.

Identifiers

PMID35906244
PMCPMC9334537
OpenAlexW4288422760

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.