Effect of Previous-Year Vaccination on the Efficacy, Immunogenicity, and Safety of High-Dose Inactivated Influenza Vaccine in Older Adults

被引:27
|
作者
DiazGranados, Carlos A. [1 ]
Dunning, Andrew J. [1 ]
Robertson, Corwin A. [1 ]
Talbot, H. Keipp [2 ]
Landolfi, Victoria [1 ]
Greenberg, David P. [1 ,3 ]
机构
[1] Sanofi Pasteur, 1 Discovery Dr, Swiftwater, PA 18370 USA
[2] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[3] Univ Pittsburgh, Sch Med, Dept Pediat, Pittsburgh, PA 15260 USA
关键词
human influenza vaccines; inactivated vaccines; phase 3 clinical trial; aged; age 80 and older; IMMUNIZATION; PREVENTION; PROTECTION; VIRUS;
D O I
10.1093/cid/ciw085
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. High-dose inactivated influenza vaccine (IIV-HD) is an alternative to the standard-dose inactivated influenza vaccine (IIV-SD) in the United States for influenza prevention in older adults. IIV-HD improved efficacy relative to IIV-SD in a randomized controlled trial. Recent observational studies suggest that previous influenza vaccination may influence the immunogenicity and effectiveness of current-season vaccination. Methods. The original study was a double-blind, randomized trial comparing IIV-HD to IIV-SD in adults aged >= 65 years over 2 influenza seasons. A subset of year 1 (Y1) participants reenrolled in year 2 (Y2), receiving vaccine by random assignment in both years. We evaluated the effect of Y1 vaccination on Y2 relative vaccine efficacy (VE), immunogenicity (hemagglutination inhibition [HAI] titers), and safety among reenrolled participants. Results. Of 14 500 Y1 participants, 7643 reenrolled in Y2. Relative to participants who received IIV-SD both seasons, VE was higher for IIV-HD vaccinees in Y2 (28.3% overall; 25.1% for Y1 IIV-HD, Y2 IIV-HD; and 31.6% for Y1 IIV-SD, Y2 IIV-HD). In multivariate logistic regression models, Y1 vaccine was not a significant modifier of Y2 VE (P = .43), whereas Y2 IIV-HD remained significantly associated with lower influenza risk (P = .043). Compared to administration of IIV-SD in both years, postvaccination HAI titers were significantly higher for patterns that included IIV-HD in Y2. No safety concerns were raised with IIV-HD revaccination. Conclusions. IIV-HD is likely to provide clinical benefit over IIV-SD irrespective of previous-season vaccination with IIV-HD or IIV-SD. IIV-HD consistently improved immune responses, and no safety concerns emerged in the context of IIV-HD revaccination.
引用
收藏
页码:1092 / 1099
页数:8
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