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Updated: Sep 20, 2026

Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
[Development of a live culture of cold-adapted reassortant influenza vaccines]
Abstract:
Optimal conditions for the cultivation of the MDCK cell lines in the laboratory spinner or by using the Eagle-MEM with or without fetal serum were worked out. The cold-adapted reassortant vaccine strains of virus influenza A/H1N1, A/H3N2 and B are well replicated in the MDCK cells both in a monolayer and in the spinner by using the serum-free medium. A maximum virus titer depends on a multiplicity of infection used in a fetal medium and on the addition of trypsin. Under the optimal conditions, the titer of the studied cold-adapted reassortants, while using a serum-free medium, reaches as much as 10(9.0)-10(9.5) EID50/ml.
Insights
Optimal conditions were determined for cultivating Madin-Darby Canine Kidney (MDCK) cells for influenza virus vaccine production. These findings enable high-titer replication of influenza A (H1N1, H3N2) and B virus strains using serum-free media.
Area of Science:
- Virology
- Cell Biology
- Biotechnology
Context:
- Optimizing cell culture conditions is crucial for efficient vaccine production.
- Madin-Darby Canine Kidney (MDCK) cells are widely used for influenza virus propagation.
- Serum-free media are increasingly preferred for large-scale cell culture to reduce costs and simplify purification.
Purpose:
- To establish optimal conditions for Madin-Darby Canine Kidney (MDCK) cell cultivation.
- To evaluate the replication efficiency of influenza virus strains in MDCK cells under various conditions.
- To determine the maximum virus titer achievable in serum-free media.
Summary:
- Optimal conditions for Madin-Darby Canine Kidney (MDCK) cell cultivation in laboratory spinners and monolayers were established.
- Cold-adapted reassortant vaccine strains of influenza A (H1N1, H3N2) and B viruses replicated efficiently in MDCK cells using serum-free Eagle-MEM.
- Maximum virus titers, dependent on multiplicity of infection and trypsin addition, reached 10(9.0)-10(9.5) EID50/ml under optimized serum-free conditions.
Impact:
- Provides a scalable and efficient method for producing influenza virus vaccine seed stocks.
- Facilitates the development of cost-effective and high-yield influenza vaccines.
- Contributes to the preparedness for influenza pandemics through improved vaccine manufacturing processes.
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