Production of a foot-and-mouth disease vaccine antigen using suspension-adapted BHK-21 cells in a bioreactor

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dc.contributor.authorSoonyong Park-
dc.contributor.authorJi Yul Kim-
dc.contributor.authorKyoung Hwa Ryu-
dc.contributor.authorA Y Kim-
dc.contributor.authorJaemun Kim-
dc.contributor.authorY J Ko-
dc.contributor.authorEun Gyo Lee-
dc.date.accessioned2021-06-01T03:30:33Z-
dc.date.available2021-06-01T03:30:33Z-
dc.date.issued2021-
dc.identifier.issn2076-393X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24360-
dc.description.abstractThe baby hamster kidney-21 (BHK-21) cell line is a continuous cell line used to propagate foot-and-mouth disease (FMD) virus for vaccine manufacturing. BHK-21 cells are anchorage-dependent, although suspension cultures would enable rapid growth in bioreactors, large-scale virus propagation, and cost-effective vaccine production with serum-free medium. Here, we report the successful adaptation of adherent BHK-21 cells to growth in suspension to a viable cell density of 7.65 × 106 cells/mL on day 3 in serum-free culture medium. The suspension-adapted BHK-21 cells showed lower adhesion to five types of extracellular matrix proteins than adherent BHK-21 cells, which contributed to the suspension culture. In addition, a chemically defined medium (selected by screening various prototype media) led to increased FMD virus production yields in the batch culture, even at a cell density of only 3.5 × 106 cells/mL. The suspension BHK-21 cell culture could be expanded to a 200 L bioreactor from a 20 mL flask, which resulted in a comparable FMD virus titer. This platform technology improved virus productivity, indicating its potential for enhancing FMD vaccine production.-
dc.publisherMDPI-
dc.titleProduction of a foot-and-mouth disease vaccine antigen using suspension-adapted BHK-21 cells in a bioreactor-
dc.title.alternativeProduction of a foot-and-mouth disease vaccine antigen using suspension-adapted BHK-21 cells in a bioreactor-
dc.typeArticle-
dc.citation.titleVaccines-
dc.citation.number5-
dc.citation.endPage505-
dc.citation.startPage505-
dc.citation.volume9-
dc.contributor.affiliatedAuthorSoonyong Park-
dc.contributor.affiliatedAuthorJi Yul Kim-
dc.contributor.affiliatedAuthorKyoung Hwa Ryu-
dc.contributor.affiliatedAuthorJaemun Kim-
dc.contributor.affiliatedAuthorEun Gyo Lee-
dc.contributor.alternativeName박순용-
dc.contributor.alternativeName김지율-
dc.contributor.alternativeName류경화-
dc.contributor.alternativeName김아영-
dc.contributor.alternativeName김재문-
dc.contributor.alternativeName고영준-
dc.contributor.alternativeName이은교-
dc.identifier.bibliographicCitationVaccines, vol. 9, no. 5, pp. 505-505-
dc.identifier.doi10.3390/vaccines9050505-
dc.subject.keywordAdherent-
dc.subject.keywordBaby hamster kidney cell-
dc.subject.keywordFoot-and-mouth disease-
dc.subject.keywordVirus productivity-
dc.subject.keywordSuspension culture-
dc.subject.keywordVaccine-
dc.subject.localAdherent-
dc.subject.localBaby hamster kidney cell-
dc.subject.localfoot-and-mouth disease-
dc.subject.localFoot-and-Mouth Disease-
dc.subject.localFoot-and-mouth disease-
dc.subject.localVirus productivity-
dc.subject.localSuspension cultures-
dc.subject.localSuspension culture-
dc.subject.localsuspension culture-
dc.subject.localvaccine-
dc.subject.localvaccines-
dc.subject.localVaccine-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
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