Evidence map›Paper›PMID 35169113›Full record

ArticleCell discovery2022

Design of a mutation-integrated trimeric RBD with broad protection against SARS-CoV-2.

Yu Liang, Jing Zhang, Run Yu Yuan, Mei Yu Wang, Peng He, Ji Guo Su, Zi Bo Han, Yu Qin Jin, Jun Wei Hou, Hao Zhang and 25 more

Open access · goldAbstract read
In one paragraph

Article in Cell discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 39 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

35 authors at 5 institutions in 1 country.

Yu Liang *The Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Jing Zhang *The Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Run Yu Yuan *Guangdong Provincial Institute of Public Health, Guangdong Provincial Center for Disease Control and Prevention, Guangzhou, Guangdong, China.
Mei Yu Wang *National Institute for Food and Drug Control (NIFDC), Beijing, China.
Peng He *National Institute for Food and Drug Control (NIFDC), Beijing, China.
Ji Guo SuThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Zi Bo HanThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Yu Qin JinThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Jun Wei HouThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Hao ZhangThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Xue Feng ZhangThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Shuai ShaoThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Ya Nan HouThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Zhao Ming LiuThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Li Fang DuThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Fu Jie ShenThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Wei Min ZhouNational Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China.
Ke XuNational Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China.
Ru Qin GaoQingdao Centers for Disease Control and Prevention, Qingdao, Shandong, China.
Fang TangThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Ze Hua LeiThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Shuo LiuNational Institute for Food and Drug Control (NIFDC), Beijing, China.
Wei ZhenNational Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China.
Jin Juan WuThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Xiang ZhengThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Ning LiuThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Shi ChenThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Zhi Jing MaThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Fan ZhengThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Si Yu RenThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China.
Zhong Yu HuNational Institute for Food and Drug Control (NIFDC), Beijing, China. huzhy@nifdc.org.cn.
Wei Jin HuangNational Institute for Food and Drug Control (NIFDC), Beijing, China. huangweijin@nifdc.org.cn.ORCID http://orcid.org/0000-0002-4246-8889
Gui Zhen WuNational Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China. wugz@ivdc.chinacdc.cn.
Chang Wen KeGuangdong Provincial Institute of Public Health, Guangdong Provincial Center for Disease Control and Prevention, Guangzhou, Guangdong, China. kecw1965@aliyun.com.
Qi Ming LiThe Sixth Laboratory, National Vaccine and Serum Institute (NVSI), Beijing, China. liqiming189@163.com.ORCID http://orcid.org/0000-0001-8284-7106
National Vaccine and Serum Institute · CNNational Institutes for Food and Drug Control · CNChinese Center For Disease Control and Prevention · CNGuangdong Provincial Center for Disease Control and Prevention · CNQingdao Municipal Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The continuous emergence of SARS-CoV-2 variants highlights the need of developing vaccines with broad protection. Here, according to the immune-escape capability and evolutionary convergence, the representative SARS-CoV-2 strains carrying the hotspot mutations were selected. Then, guided by structural and computational analyses, we present a mutation-integrated trimeric form of spike receptor-binding domain (mutI-tri-RBD) as a broadly protective vaccine candidate, which combined heterologous RBDs from different representative strains into a hybrid immunogen and integrated immune-escape hotspots into a single antigen. When compared with a homo-tri-RBD vaccine candidate in the stage of phase II trial, of which all three RBDs are derived from the SARS-CoV-2 prototype strain, mutI-tri-RBD induced significantly higher neutralizing antibody titers against the Delta and Beta variants, and maintained a similar immune response against the prototype strain. Pseudo-virus neutralization assay demonstrated that mutI-tri-RBD also induced broadly strong neutralizing activities against all tested 23 SARS-CoV-2 variants. The in vivo protective capability of mutI-tri-RBD was further validated in hACE2-transgenic mice challenged by the live virus, and the results showed that mutI-tri-RBD provided potent protection not only against the SARS-CoV-2 prototype strain but also against the Delta and Beta variants.

Identifiers

PMID35169113
PMCPMC8847466
OpenAlexW4213205775

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.