Safety and immunogenicity of high-dose quadrivalent influenza vaccine in adults ≥65 years of age: A phase 3 randomized clinical trial

被引:47
|
作者
Chang, Lee-Jah [1 ]
Meng, Ya [1 ]
Janosczyk, Helene [1 ]
Landolfi, Victoria [1 ]
Talbot, H. Keipp [2 ]
Boone, Gary
Briskin, Toby
Cannon, Kevin
Christensen, Shane
Davis, Matthew
Miel, Emmanuel
Eck, John
Essink, Brandon
Finn, Daniel
Fried, David
Gorse, Geoffrey
Griffin, Carl
Hollister, Ripley
Jacqmein, Jeffry
Johnson, Mark
Julien, Katie
Kay, Jennifer
Kirstein, Judith
Koehler, Timothy
Levin, Michael
Martin, Earl
Matherne, Paul
Peterson, James
Poling, Terry
Saleh, Jamshid
Segall, Nathan
Seiden, David
Strout, Cynthia
Turner, Mark
Varano, Susann
Wilson, Jonathan
Winkle, Peter
Wombolt, Duane
Abel, Keshia
Babyak, Jennifer
Bethuel, Karine
Boyle, Jacqueline
Broudic, Karine
De Bruijn, Iris
De Sousa, Jennifer
Drago, Erica
Flores, Alma
Francis, Deborah
Hicks, Bryony
Fontvieille, Anne-Isabelle
机构
[1] Sanofi Pasteur, 1 Discovery Dr, Swiftwater, PA 18370 USA
[2] Vanderbilt Univ, Med Ctr, 1761 21st Ave South, Nashville, TN 37232 USA
关键词
High-dose influenza vaccine; Quadrivalent influenza vaccine; Elderly adults; Immunogenicity; Safety; Clinical trial; EFFICACY; ANTIBODY; OLDER; CHILDREN;
D O I
10.1016/j.vaccine.2019.08.016
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: A high-dose, split-virion inactivated trivalent influenza vaccine (IIV3-HD; Fluzone (R) High-Dose, Sanofi Pasteur) is available for adults >= 65 years of age. This study examined the safety and immunogenicity of a quadrivalent high-dose split-virion inactivated influenza vaccine (IIV4-HD). Methods: This was a randomized, modified double-blind, active-controlled, multi-center trial in healthy adults >= 65 years of age. Subjects were randomized in a 4:1:1 ratio to receive a single intramuscular injection of IIV4-HD, the licensed IIV3-HD, or an IIV3-HD containing the alternate B-lineage strain. Hemagglutination inhibition (HAI), seroneutralisation, and anti-neuraminidase antibody titers were measured at baseline and day 28. Solicited reactions were collected for up to 7 days, unsolicited adverse events up to 28 days, and serious adverse events up to 180 days. The primary immunogenicity objective was to demonstrate that IIV4-HD induces HAI geometric mean titers (GMTs) and seroconversion rates that are non-inferior to those induced by IIV3-HD. Secondary objectives were to describe the safety of IIV4-HD and IIV3-HD and to demonstrate that IIV4-HD induces HAI GMTs and seroconversion rates that are superior to those induced by IIV3-HD not containing the same B-lineage strain. Results: The study included 2670 adults >= 65 years of age. For all four strains, HAI GMTs and seroconversion rates induced by IIV4-HD were non-inferior to those induced by IIV3-HDs containing the same strains. For both B strains, HAI GMTs and seroconversion rates induced by IIV4-HD were superior to those induced by IIV3-HD not containing the same B-lineage strain. Seroneutralisation and anti-neuraminidase antibody responses, measured in a subset of subjects, were similar. No new safety concerns were identified, and the safety profiles of IIV4-HD and IIV3-HD were similar. Conclusions: Adding a second B strain in IIV4-HD resulted in improved immunogenicity against the added strain without compromising the immunogenicity of the other strains or the vaccine's tolerability. (C) 2019 The Author(s). Published by Elsevier Ltd.
引用
收藏
页码:5825 / 5834
页数:10
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