Safety and immunogenicity of a high dosage trivalent influenza vaccine among elderly subjects
- PMID: 17913310
- PMCID: PMC2243220
- DOI: 10.1016/j.vaccine.2007.08.042
Safety and immunogenicity of a high dosage trivalent influenza vaccine among elderly subjects
Abstract
To improve immune responses to influenza vaccine, a trivalent inactivated vaccine containing 60 microg of the HA of each component (A/H3N2, A/H1N1, B) was compared to a licensed vaccine containing 15 microg of the HA of each. More local and systemic reactions were reported by subjects given the high dosage but only local pain and myalgias were significantly increased. The high dosage vaccine induced a higher frequency of serum antibody increases (> or =4-fold) in both hemagglutination-inhibiting (HAI) and neutralization tests for all three vaccine viruses in the total group as well as subjects vaccinated and those not vaccinated the previous year. Mean titers of antibody attained, the magnitude of antibody increases and the frequencies of persons with final HAI antibody titers > or =1:32, > or =1:64, and > or =1:128 were all greater for the high dosage group in both serologic tests, for all groups, and for all vaccine viruses. These increased immune responses should provide increased protection against influenza in the elderly.
Conflict of interest statement
Conflict of interest: Robert B. Couch has served as a consultant to GlaxoSmithKline, Vaxinnate and Dynavax.
Rebecca Brady receives funding to conduct clinical research studies from GlaxoSmithKline.
Robert Edelman is a consultant to Acambis, Inc.
Robert Belshe is a consultant to Merck and Medimmune, and is a speaker for Merck, Medimmune and sanofi pasteur.
Jose Capellan is an employee and investor of sanofi pasteur
Fred Ruben is an employee and investor of sanofi pasteur
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Comment in
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Influenza vaccine dosages.Vaccine. 2008 May 2;26(19):2305-6. doi: 10.1016/j.vaccine.2008.03.007. Epub 2008 Mar 27. Vaccine. 2008. PMID: 18407384 No abstract available.
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