Evidence map›Paper›PMID 35891268›Full record

ArticleVaccines2022

SARS-CoV-2 Doggybone DNA Vaccine Produces Cross-Variant Neutralizing Antibodies and Is Protective in a COVID-19 Animal Model.

Eric M Mucker, Rebecca L Brocato, Lucia M Principe, Robert K Kim, Xiankun Zeng, Jeffrey M Smith, Steven A Kwilas, Sungwon Kim, Helen Horton, Lisa Caproni and 1 more

Abstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

11 authors.

Eric M MuckerVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.ORCID 0000-0002-4656-5379
Rebecca L BrocatoVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.ORCID 0000-0003-4377-0710
Lucia M PrincipeVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Robert K KimPathology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.ORCID 0000-0002-1730-2860
Xiankun ZengPathology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Jeffrey M SmithVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Steven A KwilasVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Sungwon KimTouchlight Genetics, Ltd., London TW12 2ER, UK.ORCID 0000-0001-8862-5790
Helen HortonTouchlight Genetics, Ltd., London TW12 2ER, UK.
Lisa CaproniTouchlight Genetics, Ltd., London TW12 2ER, UK.
Jay W HooperVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.ORCID 0000-0002-4475-0415

Funding

Defense Health Agency 188155773
6 · The paper itself

Abstract

To combat the COVID-19 pandemic, an assortment of vaccines has been developed. Nucleic acid vaccines have the advantage of rapid production, as they only require a viral antigen sequence and can readily be modified to detected viral mutations. Doggybone™ DNA vaccines targeting the spike protein of SARS-CoV-2 have been generated and compared with a traditionally manufactured, bacterially derived plasmid DNA vaccine that utilizes the same spike sequence. Administered to Syrian hamsters by jet injection at two dose levels, the immunogenicity of both DNA vaccines was compared following two vaccinations. Immunized hamsters were then immunosuppressed and exposed to SARS-CoV-2. Significant differences in body weight were observed during acute infection, and lungs collected at the time of euthanasia had significantly reduced viral RNA, infectious virus, and pathology compared with irrelevant DNA-vaccinated controls. Moreover, immune serum from vaccinated animals was capable of neutralizing SARS-CoV-2 variants of interest and importance in vitro. These data demonstrate the efficacy of a synthetic DNA vaccine approach to protect hamsters from SARS-CoV-2.

Indexed as

COVID-19doggybone DNA vaccineimmunogenicitynucleic acidprotectionSARS-CoV-2vaccine

Identifiers

PMID35891268
PMCPMC9317096

What OpenQuestion holds

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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.