Evidence map›Paper›PMID 37821505›Full record

ArticleNPJ vaccines2023

A recombinant virus-like particle vaccine against adenovirus-7 induces a potent humoral response.

Ryan Mazboudi, Hannah Mulhall Maasz, Matthew D Resch, Ke Wen, Paul Gottlieb, Aleksandra Alimova, Reza Khayat, Natalie D Collins, Robert A Kuschner, Jose M Galarza

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

10 authors at 3 institutions in 1 country.

Ryan Mazboudi *TechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY, 10523, USA.
Hannah Mulhall Maasz *TechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY, 10523, USA.
Matthew D Resch *TechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY, 10523, USA.ORCID http://orcid.org/0000-0001-5346-3023
Ke Wen *TechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY, 10523, USA.ORCID http://orcid.org/0000-0002-4038-1448
Paul GottliebCUNY School of Medicine, The City College of New York, New York, NY, 10031, USA.
Aleksandra AlimovaCUNY School of Medicine, The City College of New York, New York, NY, 10031, USA.
Reza KhayatDepartment of Chemistry and Biochemistry, The City College of New York, New York, NY, 10031, USA.
Natalie D CollinsViral Diseases Branch, Walter Reed Army Institute for Research, Silver Spring, MD, 20910, USA.
Robert A KuschnerViral Diseases Branch, Walter Reed Army Institute for Research, Silver Spring, MD, 20910, USA.
Jose M GalarzaTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY, 10523, USA. jmgalarza@technovax.com.ORCID http://orcid.org/0000-0002-4661-509X
TechnoVax (United States) · USCity College of New York · USWalter Reed Army Institute of Research · US

Funding

U.S. Department of Defense (United States Department of Defense) W81XH19C0169
6 · The paper itself

Abstract

Adenoviruses (AdVs) cause infections in humans that range from mild to severe, and can cause outbreaks particularly in close contact settings. Several human AdV types have been identified, which can cause a wide array of clinical manifestations. AdV types 4 and 7 (AdV-4 and AdV-7), which are among the most commonly circulating types in the United States, are known to cause acute respiratory disease that can result in hospitalization and rarely, death. Currently, the only vaccines approved for use in humans are live virus vaccines against AdV-4 and AdV-7, though these vaccines are only authorized for use in U.S. military personnel. While they are efficacious, use of these live virus vaccines carries considerable risks of vaccine-associated viral shedding and recombination. Here, we present an alternative vaccination strategy against AdV-7 using the virus-like particle platform (AdVLP-7). We describe the production of stable recombinant AdVLP-7, and demonstrate that AdVLP-7 is structurally analogous to wild-type AdV-7 virions (WT AdV-7). Preclinical immunogenicity studies in mice show that AdVLP-7 elicits a potent humoral immune response, comparable to that observed in mice immunized with WT AdV-7. Specifically, AdVLP-7 induces high titers of antibodies against AdV-7-specific antigens that can effectively neutralize AdV-7.

Identifiers

PMID37821505
PMCPMC10567840
OpenAlexW4387521609

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.