Evidence map›Paper›PMID 35799178›Full record

ArticleJournal of biomedical science2022

A booster dose of Delta × Omicron hybrid mRNA vaccine produced broadly neutralizing antibody against Omicron and other SARS-CoV-2 variants.

I-Jung Lee, Cheng-Pu Sun, Ping-Yi Wu, Yu-Hua Lan, I-Hsuan Wang, Wen-Chun Liu, Joyce Pei-Yi Yuan, Yu-Wei Chang, Sheng-Che Tseng, Szu-I Tsung and 31 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  6. Observational
  7. Development of AAV-delivered broadly neutralizing anti-human ACE2 antibodies against SARS-CoV-2 variants.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
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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

41 authors at 6 institutions in 1 country.

I-Jung LeeInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Cheng-Pu Sun *Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Ping-Yi Wu *Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Yu-Hua LanInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
I-Hsuan WangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Wen-Chun LiuBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Joyce Pei-Yi YuanBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Yu-Wei ChangBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Sheng-Che TsengInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Szu-I TsungInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Yu-Chi ChouBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Monika KumariInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Yin-Shiou LinBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Hui-Feng ChenBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Tsung-Yen ChenBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Chih-Chao LinBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Chi-Wen ChiuInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chung-Hsuan HsiehInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Cheng-Ying ChuangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chao-Min ChengBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Hsiu-Ting LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Wan-Yu ChenInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Fu-Fei HsuBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Ming-Hsiang HongBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Chun-Che LiaoInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chih-Shin ChangBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Jian-Jong LiangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Hsiu-Hua MaGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Ming-Tsai ChiangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Hsin-Ni LiaoInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Hui-Ying KoInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Liang-Yu ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Yi-An KoBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Pei-Yu YuInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Tzu-Jing YangInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Po-Cheng ChiangBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Shang-Te HsuInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Yi-Ling LinInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chong-Chou LeeBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Han-Chung WuBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Mi-Hua TaoInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan. bmtao@ibms.sinica.edu.tw.ORCID http://orcid.org/0000-0002-4307-5729
Institute of Biomedical Sciences, Academia Sinica · TWAcademia Sinica · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TWNational Taiwan University · TWInstitute of Biological Chemistry, Academia Sinica · TWGenomics Research Center, Academia Sinica · TW

Funding

Institute of Biomedical Sciences, Academia Sinica AS-KPQ-110-EIMDInstitute of Biomedical Sciences, Academia Sinica AS-KPQ-111-KNT
6 · The paper itself

Abstract

backgroundWith the continuous emergence of new SARS-CoV-2 variants that feature increased transmission and immune escape, there is an urgent demand for a better vaccine design that will provide broader neutralizing efficacy.

methodsWe report an mRNA-based vaccine using an engineered "hybrid" receptor binding domain (RBD) that contains all 16 point-mutations shown in the currently prevailing Omicron and Delta variants.

resultsA booster dose of hybrid vaccine in mice previously immunized with wild-type RBD vaccine induced high titers of broadly neutralizing antibodies against all tested SARS-CoV-2 variants of concern (VOCs). In naïve mice, hybrid vaccine generated strong Omicron-specific neutralizing antibodies as well as low but significant titers against other VOCs. Hybrid vaccine also elicited CD8+/IFN-γ+ T cell responses against a conserved T cell epitope present in wild type and all VOCs.

conclusionsThese results demonstrate that inclusion of different antigenic mutations from various SARS-CoV-2 variants is a feasible approach to develop cross-protective vaccines.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesHumansMicemRNA VaccinesVaccines, SyntheticAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesmRNA VaccinesVaccines, SyntheticBooster doseCOVID-19Cross-protectivityHybrid vaccinemRNA vaccineNext generation vaccineOmicron vaccineSARS-CoV-2Variants of concern

Identifiers

PMID35799178
PMCPMC9261010
OpenAlexW4284666007

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.