Partial protection induced by 2011–2012 influenza vaccine against serologically evidenced A(H3N2) influenza virus infections in elderly institutionalized people

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Abstract

Ninety-two institutionalized elderly subjects were vaccinated with trivalent influenza inactivated vaccine available for the 2011–2012 season, characterized by a prevalent circulation of A(H3N2) influenza viruses (A/Victoria/208-clade) presenting antigenic and genetic patterns different from the A(H3N2) vaccine component (A/Perth/16/2009-clade). Haemagglutination inhibiting (HI) antibody titers were determined in sera collected before, 1 and 6 months after vaccination and patients were considered positive for serological evidence of recent infection if they had a seroconversion on comparing HI titers found in sera collected 1 and 6months after vaccination. No seroconversions were found against A(H1N1) and B vaccine components. Instead 17 volunteers seroconverted against all or at least some of the different A(H3N2) antigens examined, i.e. the 2011–2012 (A/Perth/16/2009) and the 2012–2013 (A/Victoria/361/2011) vaccine strains and four drifted viruses belonging to the A/Victoria/208-clade circulating in the area were the elderly people were living. The results obtained suggest that influenza infections in the vaccinated volunteers might be due both to a poor match between vaccine and circulating A(H3N2) viruses, since 1 month after vaccination 15 of the 17 volunteers had post-vaccination HI titers considered protective (≥40) against the A(H3N2) vaccine antigen, but not always against the epidemic strains, and to a waning of vaccine induced immune response, since 6 months after vaccination HI titers of non-infected volunteers were found to be decreased as compared with those found 1 month after vaccination.

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Camilloni, B., Basileo, M., Menculini, G., Tozzi, P., & Iorio, A. M. (2016). Partial protection induced by 2011–2012 influenza vaccine against serologically evidenced A(H3N2) influenza virus infections in elderly institutionalized people. In Advances in Experimental Medicine and Biology (Vol. 897, pp. 45–53). Springer Science and Business Media, LLC. https://doi.org/10.1007/5584_2015_5003

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