AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Robinson, D. M.
Right arrow Articles by Hetrick, F. M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Robinson, D. M.
Right arrow Articles by Hetrick, F. M.
Agricola
Right arrow Articles by Robinson, D. M.
Right arrow Articles by Hetrick, F. M.

 Previous Article  |  Next Article 

Appl Environ Microbiol. 1966 November; 14(6): 1011-1014
Copyright © 1966 American Society for Microbiology. All Rights Reserved.

Western Equine Encephalomyelitis Vaccine Produced in Chick Embryo Cell Cultures

David M. Robinson1, Sanford Berman, Joseph P. Lowenthal and Frank M. Hetrick2

Department of Biologics Research, Division of Veterinary Medicine, Walter Reed Army Institute of Research, Washington, D.C.

ABSTRACT

A method was developed for production of a freeze-dried Western equine encephalomyelitis vaccine from virus propagated in chick embryo cell culture monolayers maintained with a serum-free medium. A sufficient concentration of virus accumulated in the cell culture fluids prior to the occurrence of viral cytopathology to permit the production of a vaccine relatively free from serum and cellular proteins. Inoculation with two mouse LD50 doses of virus per 100 tissue culture cells was found to yield reproducible high virus titers at a convenient harvest time. These harvests were inactivated at 22 C by 0.05% formalin within 48 hr. Potency test results, as measured by the protection of immunized guinea pigs against an intracerebral virus challenge, indicated that the vaccine produced from the virus propagated in cell culture was equal in potency to a lot of whole chick embryo vaccine used to immunize laboratory and field workers subject to a high risk of infection.


FOOTNOTES

1 Present address: Department of Microbiology, University of Maryland, College Park.

2 Associate Professor of Microbiology, Department of Microbiology, University of Maryland, College Park.


Appl Environ Microbiol. 1966 November; 14(6): 1011-1014
Copyright © 1966 American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 1966 by the American Society for Microbiology. All rights reserved.