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Development of multivalent SARS-CoV-2 virus-like particle vaccine candidates
ID Bezeljak, Urban (Author), ID Jerman, Alexander (Author), ID Kobal, Tina (Author), ID Birsa, Elfi (Author), ID Lokar Kosmač, Martina (Author), ID Žiberna, Rok (Author), ID Lokar, Krista (Author), ID Janež, Nikolaja (Author), ID Ravlić, Sanda (Author), ID Halassy, Beata (Author), ID Kolenc, Marko (Author), ID Triglav, Tina (Author), ID Draksler, Urška (Author), ID Horvat, Simon (Author), ID Peterka, Matjaž (Author)

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Abstract
The novel betacoronavirus SARS-CoV-2 emerged in late 2019, causing the global health threat of COVID-19. Over the past years, it has infected over 700 million people worldwide, resulting in 7 million deaths. Clearly, a potent and safe vaccine that guarantees long-lasting protection against novel virus strains is desperately needed to curb and eliminate the pandemic. Here, we present the development and scalable purification of an advanced coronavirus-like particle (CoVLP) vaccine candidates derived from SARS-CoV-2 structural proteins. Highly pure and concentrated particles were produced from insect cell culture through sequential chromatography purification, employing hydrophobic and ion exchange monolithic columns. This strategy enables reliable scalability for production, supporting both preclinical and future clinical trials. The purified nanoparticles closely mimic coronavirus morphology and molecular composition, as determined by transmission electron microscopy. CoVLPs induced robust multivalent neutralizing immunity in mice against native SARS-CoV-2 in combination with squalene-based emulsion adjuvant. The isolated multivalent CoVLPs, covering a broad spectrum of viral antigens, represent a promising next-generation COVID-19 vaccine candidate, particularly considering the increasing threat of vaccine-evading mutations and waning immunity.

Language:English
Keywords:virus-like particles, SARS-CoV-2, vaccine candidate, monolith chromatography, insect cell culture
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
BF - Biotechnical Faculty
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:9 str.
Numbering:Vol. 61, art. 127394
PID:20.500.12556/RUL-170197 This link opens in a new window
UDC:577
ISSN on article:1873-2518
DOI:10.1016/j.vaccine.2025.127394 This link opens in a new window
COBISS.SI-ID:240180739 This link opens in a new window
Publication date in RUL:02.07.2025
Views:304
Downloads:66
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Record is a part of a journal

Title:Vaccine
Publisher:Elsevier Ltd.
ISSN:1873-2518
COBISS.SI-ID:520050201 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:biokemija, cepiva, SARS-CoV-2

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