Evidence map›Paper›PMID 36436305›Full record

ArticleBiomaterials2023

Respiratory mucosal vaccination of peptide-poloxamine-DNA nanoparticles provides complete protection against lethal SARS-CoV-2 challenge.

Si Sun, Entao Li, Gan Zhao, Jie Tang, Qianfei Zuo, Larry Cai, Chuanfei Xu, Cheng Sui, Yangxue Ou, Chang Liu and 15 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  7. FPharmaceutics · 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

25 authors at 7 institutions in 4 countries.

Si SunNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Entao LiKey Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Gan ZhaoAdvaccine (Suzhou) Biopharmaceuticals Co., Ltd, Suzhou, China.
Jie TangAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia.
Qianfei ZuoNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Larry CaiAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia.
Chuanfei XuNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Cheng SuiAdvaccine (Suzhou) Biopharmaceuticals Co., Ltd, Suzhou, China.
Yangxue OuNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Chang LiuNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Haibo LiNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Yuan DingAdvaccine (Suzhou) Biopharmaceuticals Co., Ltd, Suzhou, China.
Chao LiNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Dongshui LuNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Weijun ZhangNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Ping LuoNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Ping ChengNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China.
Yuwei GaoKey Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Changchun TuKey Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Bruno PitardImmunology and New Concepts in ImmunoTherapy, INSERM, CNRS, Nantes Université, Univ Angers, Nantes, France.
Joseph RoseneckerDepartment of Pediatrics, Ludwig-Maximilians University of Munich, Munich, Germany.
Bin WangAdvaccine (Suzhou) Biopharmaceuticals Co., Ltd, Suzhou, China; Key Laboratory of Medical Molecular Virology of MOH and MOE and Department of Medical Microbiology and Parasitology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Yan LiuKey Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China. Electronic address: liu820512@163.com.
Quanming ZouNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China. Electronic address: qmzou2007@163.com.
Shan GuanNational Engineering Research Center of Immunological Products, Third Military Medical University, Chongqing, China. Electronic address: guanshan87@163.com.
Army Medical University · CNChinese Academy of Agricultural Sciences · CNThe University of Queensland · AUCentre National de la Recherche Scientifique · FRChangchun Institute of Optics, Fine Mechanics and Physics · CNLudwig-Maximilians-Universität München · DEShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ongoing SARS-CoV-2 pandemic represents a brutal reminder of the continual threat of mucosal infectious diseases. Mucosal immunity may provide robust protection at the predominant sites of SARS-CoV-2 infection. However, it remains unclear whether respiratory mucosal administration of DNA vaccines could confer protective immune responses against SARS-CoV-2 challenge due to insurmountable barriers posed by the airway. Here, we applied self-assembled peptide-poloxamine nanoparticles with mucus-penetrating properties for pulmonary inoculation of a COVID-19 DNA vaccine (pSpike/PP-sNp). The pSpike/PP-sNp not only displays superior gene transfection and favorable biocompatibility in the mouse airway, but also promotes a tripartite immunity consisting of systemic, cellular, and mucosal immune responses that are characterized by mucosal IgA secretion, high levels of neutralizing antibodies, and resident memory phenotype T-cell responses in the lungs of mice. Most importantly, immunization with pSpike/PP-sNp completely eliminates SARS-CoV-2 infection in both upper and lower respiratory tracts and enables 100% survival rate of mice following lethal SARS-CoV-2 challenge. Our findings indicate PP-sNp is a promising platform in mediating DNA vaccines to elicit all-around mucosal immunity against SARS-CoV-2.

Indexed as

COVID-19NanoparticlesVaccines, DNAAnimalsAntibodies, NeutralizingAntibodies, ViralDNAMicePeptidesSARS-CoV-2VaccinationAntibodies, NeutralizingAntibodies, ViralDNAPeptidesVaccines, DNADNA vaccineMucosal vaccineNonviral delivery systemPulmonary deliverySARS-CoV-2

Identifiers

PMID36436305
PMCPMC9673044
OpenAlexW4309378418

What OpenQuestion holds

Textmetadata
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.