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Sequential infection or immunization of ferrets with a series of influenza A (H3N2) strains (Report to the Medical Research Council's Sub-Committee on Influenza Vaccines (CDVIP/IV))

Published online by Cambridge University Press:  19 October 2009

C. W. Potter*
Affiliation:
University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX
R. Jennings
Affiliation:
University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX
M. J. Ali
Affiliation:
University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX
J. M. Wood
Affiliation:
Division of Viral Products, National Institute for Biological Standardization and Control, Holly Hill, Hampstead, London NW3 6RB
U. Dunleavy
Affiliation:
Division of Viral Products, National Institute for Biological Standardization and Control, Holly Hill, Hampstead, London NW3 6RB
D. A. J. Tyrrell
Affiliation:
M.R.C. Common Cold Unit, Harvard Hospital, Coombe Road, Salisbury SP2 8BW
*
*Correspondence should be addressed to Professor C. W. Potter at the above address.
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Previous studies of boys at Christ's Hospital school have indicated that annual immunization with influenza virus vaccines did not significantly reduce the total incidence of influenza infection compared to unimmunized subjects. In view of the implications of this result, a similar study was conducted in ferrets to clarify these findings. Groups of ferrets were immunized or infected with a series of influenza A (H3N2) viruses over an 18-month period, and the immunity to subsequent live virus challenge was measured after each virus or vaccine exposure. The results indicated that live virus infection gave a more solid immunity than immunization with inactivated vaccine; and the serum haemagglutination-inhibiting antibody response was greater following immunization than following infection. In addition, differences in immunity could not be explained by measurements of cross-reacting and specific antibody, since the incidence of these antibodies was similar in both infected and immunized animals. The results do not suggest an explanation for the different levels of immunity induced following infection or immunization or the results obtained from the Christ's Hospital study. However, the relative contribution of various immune responses to virus or virus antigen is discussed, and it is suggested that the difference in immunity may lie in the ability of live virus infection to stimulate local antibody.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1987

References

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