<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(1)</volume><submitter>Alpuche-Lazcano SP</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>As the COVID-19 pandemic continues to evolve, novel vaccines need to be developed that are readily manufacturable and provide clinical efficacy against emerging SARS-CoV-2 variants. Virus-like particles (VLPs) presenting the spike antigen at their surface offer remarkable benefits over other vaccine antigen formats; however, current SARS-CoV-2 VLP vaccines candidates in clinical development suffer from challenges including low volumetric productivity, poor spike antigen density, expression platform-driven divergent protein glycosylation and complex upstream/downstream processing requirements. Despite their extensive use for therapeutic protein manufacturing and proven ability to produce enveloped VLPs, Chinese Hamster Ovary (CHO) cells are rarely used for the commercial </pubmed_abstract><journal>Communications medicine</journal><pagination>116</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10447459</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preclinical evaluation of manufacturable SARS-CoV-2 spike virus-like particles produced in Chinese Hamster Ovary cells.</pubmed_title><pmcid>PMC10447459</pmcid><pubmed_authors>Star A</pubmed_authors><pubmed_authors>Cass B</pubmed_authors><pubmed_authors>Durocher Y</pubmed_authors><pubmed_authors>Maltais JS</pubmed_authors><pubmed_authors>Dudani R</pubmed_authors><pubmed_authors>Cui K</pubmed_authors><pubmed_authors>Cho JY</pubmed_authors><pubmed_authors>Blouin J</pubmed_authors><pubmed_authors>Stuible M</pubmed_authors><pubmed_authors>Alpuche-Lazcano SP</pubmed_authors><pubmed_authors>Tran A</pubmed_authors><pubmed_authors>Zoubchenok D</pubmed_authors><pubmed_authors>Duque D</pubmed_authors><pubmed_authors>McCluskie MJ</pubmed_authors><pubmed_authors>Hrapovic S</pubmed_authors><pubmed_authors>Haqqani A</pubmed_authors><pubmed_authors>Renner TM</pubmed_authors><pubmed_authors>Kelly J</pubmed_authors><pubmed_authors>Robotham A</pubmed_authors><pubmed_authors>Akache B</pubmed_authors><pubmed_authors>Wang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preclinical evaluation of manufacturable SARS-CoV-2 spike virus-like particles produced in Chinese Hamster Ovary cells.</name><description>&lt;h4>Background&lt;/h4>As the COVID-19 pandemic continues to evolve, novel vaccines need to be developed that are readily manufacturable and provide clinical efficacy against emerging SARS-CoV-2 variants. Virus-like particles (VLPs) presenting the spike antigen at their surface offer remarkable benefits over other vaccine antigen formats; however, current SARS-CoV-2 VLP vaccines candidates in clinical development suffer from challenges including low volumetric productivity, poor spike antigen density, expression platform-driven divergent protein glycosylation and complex upstream/downstream processing requirements. Despite their extensive use for therapeutic protein manufacturing and proven ability to produce enveloped VLPs, Chinese Hamster Ovary (CHO) cells are rarely used for the commercial </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-04-29T02:25:46.383Z</modification><creation>2025-02-19T04:01:44.253Z</creation></dates><accession>S-EPMC10447459</accession><cross_references><pubmed>37612423</pubmed><doi>10.1038/s43856-023-00340-7</doi></cross_references></HashMap>