2015
DOI: 10.1016/j.vaccine.2015.01.025
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Safety and immunogenicity of a quadrivalent intradermal influenza vaccine in adults

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Cited by 33 publications
(25 citation statements)
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“…As a result, this platform can be much more nimble than classical approaches based on egg-or tissue culture-adapted viruses. Herein we report the results of a phase 1-2 dose-escalation trial of a QVLP vaccine that was both well- QIVs and commercial TIVs [8,9,39,40]. It was also reassuring that we did not see either worsening or induction of allergic symptoms following QVLP exposure and there was no evidence of a potentially immunopathologic IgE response to plant-origin carbohydrate motifs present on the QVLP vaccine.…”
Section: Discussionmentioning
confidence: 83%
“…As a result, this platform can be much more nimble than classical approaches based on egg-or tissue culture-adapted viruses. Herein we report the results of a phase 1-2 dose-escalation trial of a QVLP vaccine that was both well- QIVs and commercial TIVs [8,9,39,40]. It was also reassuring that we did not see either worsening or induction of allergic symptoms following QVLP exposure and there was no evidence of a potentially immunopathologic IgE response to plant-origin carbohydrate motifs present on the QVLP vaccine.…”
Section: Discussionmentioning
confidence: 83%
“…Among adults the most common safety complaints were injection-site pain and systemic reactions, such as myalgia, headaches, and fatigue (123,125,127,129,130,309). The first postlicensure safety assessment of VAERS reports covering the 2013-14 and 2014-15 seasons noted a safety profile similar to that of IIV3.…”
Section: Adultsmentioning
confidence: 99%
“…A review of VAERS reports covering the 2011-12 and 2012-13 seasons, the first two seasons that the intradermal IIV3 was available, revealed no new safety concerns (312). A randomized study comparing safety of the newer IIV4 with that of IIV3 revealed a similar adverse event profile (130).…”
Section: Adultsmentioning
confidence: 99%
“…Fluzone Intradermal Quadrivalent : This intradermal vaccine is licensed for use in adults aged 18–64 y and was evaluated in 3360 participants in one study in the US 37 . Non-inferiority was demonstrated between the intradermal F-IIV4 and intradermal IIV3 in terms of HI GMTs and SCRs to common strains, and superiority of the immune response to the added influenza type B lineage compared with 2 intradermal IIV3 formulations was also demonstrated.…”
Section: Clinical Evaluation and Characteristics Of Currently Licensementioning
confidence: 99%