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Nine mu g intradermal influenza vaccine and 15 mu g intramuscular influenza vaccine induce similar cellular and humoral immune responses in adults

机译:9微克皮内流感疫苗和15微克肌内流感疫苗在成人中诱导相似的细胞和体液免疫反应

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摘要

Intanza (R) 9 mu g (Sanofi Pasteur), a trivalent split-virion vaccine administered by intradermal (ID) injection, was approved in Europe in 2009 for the prevention of seasonal influenza in adults 18 to 59 years. Here, we examined the immune responses induced in adults by the ID 9 mu g vaccine and the standard trivalent intramuscular (IM) vaccine (Vaxigrip (R) 15 mu g, Sanofi Pasteur). This trial was a randomized, controlled, single-center, open-label study in healthy adults 18 to 40 years of age during the 2007/8 influenza season. Subjects received a single vaccination with the ID 9 mu g (n = 38) or IM 15 mu g (n = 42) vaccine. Serum, saliva, and peripheral blood mononuclear cells were collected up to 180 days post-vaccination.
机译:Intanza(R)9微克(Sanofi Pasteur)是通过皮内(ID)注射给药的三价裂殖病毒疫苗,于2009年在欧洲获准用于预防18至59岁成人的季节性流感。在这里,我们检查了ID 9μg疫苗和标准三价肌内(IM)疫苗(Vaxigrip(R)15μg,赛诺菲巴斯德(Sanofi Pasteur))在成人中诱导的免疫反应。该试验是一项在2007/8流感季节期间针对18至40岁健康成年人的随机,对照,单中心,开放标签研究。受试者接受ID 9μg(n = 38)或IM 15μg(n = 42)疫苗的单次疫苗接种。疫苗接种后180天内收集血清,唾液和外周血单核细胞。

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