Evidence map›Paper›PMID 34066016›Full record

ArticleVaccines2021

Mice Immunized with the Vaccine Candidate HexaPro Spike Produce Neutralizing Antibodies against SARS-CoV-2.

Chotiwat Seephetdee, Nattawut Buasri, Kanit Bhukhai, Kitima Srisanga, Suwimon Manopwisedjaroen, Sarat Lertjintanakit, Nut Phueakphud, Chatbenja Pakiranay, Niwat Kangwanrangsan, Sirawat Srichatrapimuk and 6 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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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

16 authors at 1 institution in 1 country.

Chotiwat SeephetdeeDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0001-7266-4744
Nattawut BuasriDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Kanit BhukhaiDepartment of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Kitima SrisangaDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Suwimon ManopwisedjaroenDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Sarat LertjintanakitDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Nut PhueakphudDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Chatbenja PakiranayDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Niwat KangwanrangsanDepartment of Pathobiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Sirawat SrichatrapimukChakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Samut Prakan 10540, Thailand.
Suppachok KirdlarpChakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Samut Prakan 10540, Thailand.
Somnuek SungkanuparphChakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Samut Prakan 10540, Thailand.
Somchai ChutipongtanateChakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Samut Prakan 10540, Thailand.ORCID 0000-0001-6398-5626
Arunee ThitithanyanontDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0002-9756-4763
Suradej HongengDepartment of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Patompon WongtrakoongateDepartment of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0001-6070-1843
Mahidol University · TH

Funding

Faculty of Medicine Ramathibodi Hospital CF63010Mahidol University NDFR 11/2563Office of National Higher Education Science Research and Innovation Policy Council by Pro-gram Management Unit for Human Resources and Institutional Development, Research and In-novation B05F630081
6 · The paper itself

Abstract

Updated and revised versions of COVID-19 vaccines are vital due to genetic variations of the SARS-CoV-2 spike antigen. Furthermore, vaccines that are safe, cost-effective, and logistic-friendly are critically needed for global equity, especially for middle- to low-income countries. Recombinant protein-based subunit vaccines against SARS-CoV-2 have been reported using the receptor-binding domain (RBD) and the prefusion spike trimers (S-2P). Recently, a new version of prefusion spike trimers, named HexaPro, has been shown to possess two RBD in the "up" conformation, due to its physical property, as opposed to just one exposed RBD found in S-2P. Importantly, this HexaPro spike antigen is more stable than S-2P, raising its feasibility for global logistics and supply chain. Here, we report that the spike protein HexaPro offers a promising candidate for the SARS-CoV-2 vaccine. Mice immunized by the recombinant HexaPro adjuvanted with aluminum hydroxide using a prime-boost regimen produced high-titer neutralizing antibodies for up to 56 days after initial immunization against live SARS-CoV-2 infection. Also, the level of neutralization activity is comparable to that of convalescence sera. Our results indicate that the HexaPro subunit vaccine confers neutralization activity in sera collected from mice receiving the prime-boost regimen.

Indexed as

HexaProSARS-CoV-2spikevaccine

Identifiers

PMID34066016
PMCPMC8151071
OpenAlexW3162710953

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.