Evidence map›Paper›PMID 36882925›Full record

ArticleHuman vaccines & immunotherapeutics2023

A trimeric spike-based COVID-19 vaccine candidate induces broad neutralization against SARS-CoV-2 variants.

Feixia Gao, Mei Zheng, Jiangfeng Fan, Yahong Ding, Xueying Liu, Min Zhang, Xin Zhang, Jinrong Dong, Xu Zhou, Jian Luo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 2 institutions in 2 countries.

Feixia GaoDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Mei ZhengDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Jiangfeng FanDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Yahong DingDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Xueying LiuDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Min ZhangDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Xin ZhangDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Jinrong DongDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Xu ZhouDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Jian LuoDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Xiuling LiDepartment of Research and Development, Shanghai Institute of Biological Products, Shanghai, China.
Shanghai Research Institute of Chemical Industry · CNBiological E (India) · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 pandemic caused by SARS-CoV-2 infection has an impact on global public health and social economy. The emerging immune escape of SARS-CoV-2 variants pose great challenges to the development of vaccines based on original strains. The development of second-generation COVID-19 vaccines to induce immune responses with broad-spectrum protective effects is a matter of great urgency. Here, a prefusion-stabilized spike (S) trimer protein based on B.1.351 variant was expressed and prepared with CpG7909/aluminum hydroxide dual adjuvant to investigate the immunogenicity in mice. The results showed that the candidate vaccine could induce a significant receptor binding domain-specific antibody response and a substantial interferon-γ-mediated immune response. Furthermore, the candidate vaccine also elicited robust cross-neutralization against the pseudoviruses of the original strain, Beta variant, Delta variant and Omicron variant. The vaccine strategy of S-trimer protein formulated with CpG7909/aluminum hydroxide dual adjuvant may be considered a means to increase vaccine effectiveness against future variants.

Indexed as

COVID-19COVID-19 VaccinesAdjuvants, ImmunologicAluminum HydroxideAnimalsAntibodies, NeutralizingAntibodies, ViralHumansMicePandemicsSARS-CoV-2Spike Glycoprotein, CoronavirusAdjuvants, ImmunologicAluminum HydroxideAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2aluminum hydroxide adjuvantCpGcross-neutralizationSARS-CoV-2S-Trimer proteinvaccine

Identifiers

PMID36882925
PMCPMC10026892
OpenAlexW4323532508

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.