Evidence map›Paper›PMID 37830223›Full record

ArticleJournal of microbiology and biotechnology2024

Comparative Biodistribution Study of Baculoviral and Adenoviral Vector Vaccines against SARS-CoV-2.

Hyeon Dong Lee, Jungmin Chun, Sehyun Kim, Nowakowska Aleksandra, Chanyeong Lee, Doyoung Yoon, Hee-Jung Lee, Young Bong Kim

Open access · greenAbstract read
In one paragraph

Article in Journal of microbiology and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

8 authors at 2 institutions in 1 country.

Hyeon Dong LeeDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Jungmin ChunDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Sehyun KimKR BioTech Co. Ltd., Seoul 05029, Republic of Korea.
Nowakowska AleksandraDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Chanyeong LeeDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Doyoung YoonDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Hee-Jung LeeDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Young Bong KimDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Konkuk University · KRSTR Biotech (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various types of vaccines have been developed against COVID-19, including vector vaccines. Among the COVID-19 vaccines, AstraZeneca's chimpanzee adenoviral vaccine was the first to be commercialized. For viral vector vaccines, biodistribution studies are critical to vaccine safety, gene delivery, and efficacy. This study compared the biodistribution of the baculoviral vector vaccine (AcHERV-COVID19) and the adenoviral vector vaccine (Ad-COVID19). Both vaccines were administered intramuscularly to mice, and the distribution of the SARS-CoV-2 S gene in each tissue was evaluated for up to 30 days. After vaccination, serum and various tissue samples were collected from the mice at each time point, and IgG levels and DNA copy numbers were measured using an enzyme-linked immunosorbent assay and a quantitative real-time polymerase chain reaction. AcHERV-COVID19 and Ad-COVID19 distribution showed that the SARS-CoV-2 spike gene remained predominantly at the injection site in the mouse muscle. In kidney, liver, and spleen tissues, the AcHERV-COVID19 group showed about 2-4 times higher persistence of the SARS-CoV-2 spike gene than the Ad-COVID19 group. The distribution patterns of AcHERV-COVID19 and Ad-COVID19 within various organs highlight their contrasting biodistribution profiles, with AcHERV-COVID19 exhibiting a broader and prolonged presence in the body compared to Ad-COVID19. Understanding the biodistribution profile of AcHERV-COVID19 and Ad-COVID19 could help select viral vectors for future vaccine development.

Indexed as

COVID-19Viral VaccinesAnimalsAntibodies, ViralCOVID-19 VaccinesHumansMiceSARS-CoV-2Tissue DistributionAntibodies, ViralCOVID-19 VaccinesViral Vaccinesadenoviral vectorbaculoviral vectorBiodistributionSARS-CoV-2vaccine

Identifiers

PMID37830223
PMCPMC10840461
OpenAlexW4387599762

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.