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Serum-Free Suspension Culture of MDCK Cells for Production of Influenza H1N1 Vaccines

Development of serum-free suspension cell culture processes is very important for influenza vaccine production. Previously, we developed a MDCK suspension cell line in a serum-free medium. In the present study, the growth kinetics of suspension MDCK cells and influenza virus production in the serum-...

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Detalles Bibliográficos
Autores principales: Huang, Ding, Peng, Wen-Juan, Ye, Qian, Liu, Xu-Ping, Zhao, Liang, Fan, Li, Xia-Hou, Kang, Jia, Han-Jing, Luo, Jian, Zhou, Lin-Ting, Li, Bei-Bei, Wang, Shi-Lei, Xu, Wen-Ting, Chen, Ze, Tan, Wen-Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634975/
https://www.ncbi.nlm.nih.gov/pubmed/26540170
http://dx.doi.org/10.1371/journal.pone.0141686
Descripción
Sumario:Development of serum-free suspension cell culture processes is very important for influenza vaccine production. Previously, we developed a MDCK suspension cell line in a serum-free medium. In the present study, the growth kinetics of suspension MDCK cells and influenza virus production in the serum-free medium were investigated, in comparison with those of adherent MDCK cells in both serum-containing and serum-free medium. It was found that the serum-free medium supported the stable subculture and growth of both adherent and suspension cells. In batch culture, for both cell lines, the growth kinetics in the serum-free medium was comparable with those in the serum-containing medium and a commercialized serum-free medium. In the serum-free medium, peak viable cell density (VCD), haemagglutinin (HA) and median tissue culture infective dose (TCID(50)) titers of the two cell lines reached 4.51×10(6) cells/mL, 2.94Log(10)(HAU/50 μL) and 8.49Log(10)(virions/mL), and 5.97×10(6) cells/mL, 3.88Log(10)(HAU/50 μL), and 10.34Log(10)(virions/mL), respectively. While virus yield of adherent cells in the serum-free medium was similar to that in the serum-containing medium, suspension culture in the serum-free medium showed a higher virus yield than adherent cells in the serum-containing medium and suspension cells in the commercialized serum-free medium. However, the percentage of infectious viruses was lower for suspension culture in the serum-free medium. These results demonstrate the great potential of this suspension MDCK cell line in serum-free medium for influenza vaccine production and further improvements are warranted.