Abstract |
Measles and mumps are common viral childhood diseases that can cause serious complications. Vaccination remains the most efficient way to control the spread of these viruses. The manufacturing capability for viral vaccines produced in embryonated hen eggs and conventional/classical cell substrates, such as chicken embryo fibroblast or primary dog kidney cell substrates, is no longer sufficient. This limitation can be overcome by utilizing other recognized cell substrates such as Madin Darby Canine Kidney (MDCK), Chinese Hamster Ovary (CHO), Vero (monkey origin) cells, MRC-5 (human diploid) or as an alternative, introducing new cell substrates of human or avian origin. A very important factor in vaccine production is the safety and immunogenicity of the final vaccine, where the proper choice of cell substrate used for virus propagation is made. All substrates used in vaccine production must be fully characterized to avoid the contamination of hidden unknown pathogens which is difficult to achieve in primary cell substrates.
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Authors | T Betáková, D Svetlíková, M Gocník |
Journal | Acta virologica
(Acta Virol)
Vol. 57
Issue 2
Pg. 91-6
( 2013)
ISSN: 0001-723X [Print] Slovakia |
PMID | 23600866
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Measles Vaccine
- Mumps Vaccine
- Viral Vaccines
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Topics |
- Animals
- Humans
- Measles
(immunology, prevention & control)
- Measles Vaccine
(immunology)
- Mumps
(immunology, prevention & control)
- Mumps Vaccine
(immunology)
- Viral Vaccines
(immunology)
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