Evidence map›Paper›PMID 35478188›Full record

ArticleSignal transduction and targeted therapy2022

Broadly neutralizing antibodies against Omicron-included SARS-CoV-2 variants induced by vaccination.

Xiangyang Chi, Yingying Guo, Guanying Zhang, Hancong Sun, Jun Zhang, Min Li, Zhengshan Chen, Jin Han, Yuanyuan Zhang, Xinghai Zhang and 19 more

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2022. 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
2.3field-weighted citation impact, top 10% 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, 23 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

29 authors at 3 institutions in 1 country.

Xiangyang Chi *Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Yingying Guo *Center for Infectious Disease Research, Westlake Laboratory of Life Sciences and Biomedicine, Key Laboratory of Structural Biology of Zhejiang Province, Institute of Biology, Westlake Institute for Advanced Study, School of Life Sciences, Westlake University, Hangzhou, 310024, Zhejiang Province, China.
Guanying Zhang *Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Hancong Sun *Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Jun Zhang *Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.ORCID 0000-0002-9650-112X
Min Li *State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, 100071, China.
Zhengshan Chen *Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Jin HanInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Yuanyuan ZhangCenter for Infectious Disease Research, Westlake Laboratory of Life Sciences and Biomedicine, Key Laboratory of Structural Biology of Zhejiang Province, Institute of Biology, Westlake Institute for Advanced Study, School of Life Sciences, Westlake University, Hangzhou, 310024, Zhejiang Province, China.
Xinghai ZhangWuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, 430071, China.
Pengfei FanInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Zhe ZhangInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Busen WangInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.ORCID 0000-0001-9041-1919
Xiaodong ZaiInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Xuelian HanState Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, 100071, China.
Meng HaoInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Ting FangInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Jinghan XuInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Shipo WuInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Yi ChenInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Yingying FangState Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, 100071, China.
Yunzhu DongInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Bingjie SunInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Jinlong ZhangInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Jianmin LiInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China.
Guangyu ZhaoState Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, 100071, China. guangyu0525@outlook.com.
Changming YuInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China. yuchangming@126.com.
Qiang ZhouCenter for Infectious Disease Research, Westlake Laboratory of Life Sciences and Biomedicine, Key Laboratory of Structural Biology of Zhejiang Province, Institute of Biology, Westlake Institute for Advanced Study, School of Life Sciences, Westlake University, Hangzhou, 310024, Zhejiang Province, China. zhouqiang@westlake.edu.cn.
Wei ChenInstitute of Biotechnology, Academy of Military Medical Sciences, Beijing, 100071, China. cw0226@foxmail.com.
Academy of Military Medical Sciences · CNWestlake University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 Omicron variant shows substantial resistance to neutralization by infection- and vaccination-induced antibodies, highlighting the demands for research on the continuing discovery of broadly neutralizing antibodies (bnAbs). Here, we developed a panel of bnAbs against Omicron and other variants of concern (VOCs) elicited by vaccination of adenovirus-vectored COVID-19 vaccine (Ad5-nCoV). We also investigated the human longitudinal antibody responses following vaccination and demonstrated how the bnAbs evolved over time. A monoclonal antibody (mAb), named ZWD12, exhibited potent and broad neutralization against SARS-CoV-2 variants Alpha, Beta, Gamma, Kappa, Delta, and Omicron by blocking the spike protein binding to the angiotensin-converting enzyme 2 (ACE2) and provided complete protection in the challenged prophylactic and therapeutic K18-hACE2 transgenic mouse model. We defined the ZWD12 epitope by determining its structure in complex with the spike (S) protein via cryo-electron microscopy. This study affords the potential to develop broadly therapeutic mAb drugs and suggests that the RBD epitope bound by ZWD12 is a rational target for the design of a broad spectrum of vaccines.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, MonoclonalAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19 VaccinesCryoelectron MicroscopyEpitopesHumansMiceSpike Glycoprotein, CoronavirusVaccinationViral Envelope ProteinsAntibodies, MonoclonalAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19 VaccinesEpitopesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Envelope Proteins

Identifiers

PMID35478188
PMCPMC9044386
OpenAlexW4225105872

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.