Evidence map›Paper›PMID 38678055›Full record

ArticleSignal transduction and targeted therapy2024

Nasal vaccination of triple-RBD scaffold protein with flagellin elicits long-term protection against SARS-CoV-2 variants including JN.1.

Xian Li, Mengxin Xu, Jingyi Yang, Li Zhou, Lin Liu, Min Li, Shasha Wang, Mei-Qin Liu, Zhixiang Huang, Zhen Zhang and 11 more

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2024. 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
7.8field-weighted citation impact, top 2% 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, 20 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

21 authors at 5 institutions in 1 country.

Xian Li *Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Mengxin Xu *School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
Jingyi Yang *Vaccine and Immunology Research Center, Translational Medical Research Institute, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China. yangjingyi@shaphc.org.
Li ZhouState Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.
Lin LiuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
Min LiVaccine and Immunology Research Center, Translational Medical Research Institute, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Shasha WangVaccine and Immunology Research Center, Translational Medical Research Institute, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Mei-Qin LiuWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Zhixiang HuangState Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.
Zhen ZhangState Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.
Shuning LiuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
Yunqi HuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
Haofeng LinWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Bowen LiuWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Ying SunAerosol Bio-Tech (Suzhou) Co., LTD, Suzhou, Jiangsu, China.
Qingguo WuVaccine and Immunology Research Center, Translational Medical Research Institute, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Zheng-Li ShiWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.ORCID 0000-0001-8089-163X
Ke LanState Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.ORCID 0000-0002-0384-8598
Yu ChenState Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China. chenyu@whu.edu.cn.ORCID 0000-0003-1300-4652
Huimin YanWuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China. yanhuimin@shaphc.org.ORCID 0000-0002-7243-8429
Yao-Qing ChenSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China. chenyaoqing@mail.sysu.edu.cn.ORCID 0000-0002-4659-1550
Chinese Academy of Sciences · CNShanghai Public Health Clinical Center · CNSun Yat-sen University · CNWuhan University · CNShenzhen University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82341041National Natural Science Foundation of China (National Science Foundation of China) 92169104
6 · The paper itself

Abstract

Developing a mucosal vaccine against SARS-CoV-2 is critical for combatting the epidemic. Here, we investigated long-term immune responses and protection against SARS-CoV-2 for the intranasal vaccination of a triple receptor-binding domain (RBD) scaffold protein (3R-NC) adjuvanted with a flagellin protein (KFD) (3R-NC + KFDi.n). In mice, the vaccination elicited RBD-specific broad-neutralizing antibody responses in both serum and mucosal sites sustained at high level over a year. This long-lasting humoral immunity was correlated with the presence of long-lived RBD-specific IgG- and IgA-producing plasma cells, alongside the Th17 and Tfh17-biased T-cell responses driven by the KFD adjuvant. Based upon these preclinical findings, an open labeled clinical trial was conducted in individuals who had been primed with the inactivated SARS-CoV-2 (IAV) vaccine. With a favorable safety profile, the 3R-NC + KFDi.n boost elicited enduring broad-neutralizing IgG in plasma and IgA in salivary secretions. To meet the challenge of frequently emerged variants, we further designed an updated triple-RBD scaffold protein with mutated RBD combinations, which can induce adaptable antibody responses to neutralize the newly emerging variants, including JN.1. Our findings highlight the potential of the KFD-adjuvanted triple-RBD scaffold protein is a promising prototype for the development of a mucosal vaccine against SARS-CoV-2 infection.

Indexed as

Administration, IntranasalAntibodies, NeutralizingAntibodies, ViralCOVID-19COVID-19 VaccinesFlagellinSARS-CoV-2AdultAnimalsFemaleHumansImmunoglobulin AImmunoglobulin GMaleMiceMiddle AgedAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesFlagellinImmunoglobulin AImmunoglobulin GSpike Glycoprotein, Coronavirus

Identifiers

PMID38678055
PMCPMC11055866
OpenAlexW4395691470

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.