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首页> 外文期刊>Vaccine >A randomized, double-blind trial to evaluate immunogenicity and safety of 13-valent pneumococcal conjugate vaccine given concomitantly with trivalent influenza vaccine in adults aged = 65 years
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A randomized, double-blind trial to evaluate immunogenicity and safety of 13-valent pneumococcal conjugate vaccine given concomitantly with trivalent influenza vaccine in adults aged = 65 years

机译:一项随机双盲试验,用于评估65岁以上成人与13价肺炎球菌结合疫苗与三价流感疫苗同时接种的免疫原性和安全性

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摘要

This randomized, double-blind study evaluated concomitant administration of 13-valent pneumococcal conjugate vaccine (PCV13) and trivalent inactivated influenza vaccine (TIV) in adults aged >= 65 years who were naive to 23-valent pneumococcal polysaccharide vaccine. Patients (N = 1160) were randomized 1:1 to receive PCV13 + TIV followed by placebo, or Placebo + TIV followed by PCV13 at 0 and 1 months, with blood draws at 0, 1, and 2 months. Slightly lower pneumococcal serotype-specific anticapsular polysaccharide immunoglobulin G geometric mean concentrations were observed with PCV13 + TIV relative to PCV13. Concomitant PCV13 + TIV demonstrates acceptable immunogenicity and safety compared with either agent given alone
机译:这项随机,双盲研究评估了初次使用23价肺炎球菌多糖疫苗的65岁以上成年人中13价肺炎球菌结合疫苗(PCV13)和三价灭活流感疫苗(TIV)的同时使用。患者(N = 1160)以1:1的比例随机分配,分别于0和1个月接受PCV13 + TIV,然后接受安慰剂,或接受安慰剂+ TIV,随后接受PCV13,分别在0、1、2个月抽血。与PCV13相比,PCV13 + TIV观察到的肺炎球菌血清型特异性抗荚膜多糖免疫球蛋白G几何平均浓度略低。与单独使用任何一种药物相比,伴随的PCV13 + TIV表现出可接受的免疫原性和安全性

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