Evidence map›Paper›PMID 33741992›Full record

ArticleNPJ vaccines2021

Human endogenous retrovirus-enveloped baculoviral DNA vaccines against MERS-CoV and SARS-CoV2.

Hansam Cho, Yuyeon Jang, Ki-Hoon Park, Hanul Choi, Aleksandra Nowakowska, Hee-Jung Lee, Minjee Kim, Min-Hee Kang, Jin-Hoi Kim, Ha Youn Shin and 2 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2021. 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
1.3field-weighted citation impact, top 17% 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, 25 citations in OpenAlex.

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  17. Advances in mRNA and other vaccines against MERS-CoV.Translational research : the journal of laboratory and clinical medicine · 2022
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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

12 authors at 2 institutions in 1 country.

Hansam Cho *KR BioTech, Seoul, Republic of Korea.
Yuyeon Jang *Department of Bio-industrial Technologies, Konkuk University, Seoul, Republic of Korea.
Ki-Hoon ParkDepartment of Bio-industrial Technologies, Konkuk University, Seoul, Republic of Korea.
Hanul ChoiDepartment of Bio-industrial Technologies, Konkuk University, Seoul, Republic of Korea.
Aleksandra NowakowskaDepartment of Biomedical Science and Engineering, Konkuk University, Seoul, Republic of Korea.
Hee-Jung LeeDepartment of Biomedical Science and Engineering, Konkuk University, Seoul, Republic of Korea.
Minjee KimDepartment of Biomedical Science and Engineering, Konkuk University, Seoul, Republic of Korea.
Min-Hee KangDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul, Republic of Korea.
Jin-Hoi KimDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-1232-5307
Ha Youn ShinDepartment of Biomedical Science and Engineering, Konkuk University, Seoul, Republic of Korea.
Yu-Kyoung OhCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Young Bong KimKR BioTech, Seoul, Republic of Korea. kimera@konkuk.ac.kr.
Konkuk University · KRSeoul National University · KR

Funding

Korea Health Industry Development Institute (KHIDI) HI15C1685Korea Health Industry Development Institute (KHIDI) HI15C2842Korea Health Industry Development Institute (KHIDI) HI18C2177
6 · The paper itself

Abstract

Here we report a recombinant baculoviral vector-based DNA vaccine system against Middle East respiratory syndrome coronavirus (MERS-CoV) and the severe acute respiratory syndrome coronavirus-2 (SARS-CoV2). A non-replicating recombinant baculovirus expressing the human endogenous retrovirus envelope gene (AcHERV) was constructed as a DNA vaccine vector for gene delivery into human cells. For MERS-CoV vaccine construction, DNA encoding MERS-CoV S-full, S1 subunit, or receptor-binding domain (RBD) was inserted into the genome of AcHERV. For COVID19 vaccine construction, DNA encoding SARS-CoV2 S-full or S1 or a MERS-CoV NTD domain-fused SARS-CoV2 RBD was inserted into the genome of AcHERV. AcHERV-DNA vaccines induce high humoral and cell-mediated immunity in animal models. In challenge tests, twice immunized AcHERV-MERS-S1 and AcHERV-COVID19-S showed complete protection against MERS-CoV and SARS-CoV2, respectively. Unlike AcHERV-MERS vaccines, AcHERV-COVID19-S provided the greatest protection against SARS-CoV2 challenge. These results support the feasibility of AcHERV-MERS or AcHERV-COVID19 vaccines in preventing pandemic spreads of viral infections.

Identifiers

PMID33741992
PMCPMC7979866
OpenAlexW3137319760

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.