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70 岁或以上健康受试者单次接种肺炎球菌结合疫苗(1×、2×或 4×)的剂量范围研究。

Dose-ranging study of a single injection of pneumococcal conjugate vaccine (1 ×, 2 ×, or 4 ×) in healthy subjects aged 70 years or older.

机构信息

Research Centre for Medical Studies, Institute of Clinical Pharmacology, Charité Universitätsmedizin Berlin, Hohenzollerndamm 2, Berlin, Germany.

出版信息

Vaccine. 2011 Jul 12;29(31):4940-6. doi: 10.1016/j.vaccine.2011.04.132. Epub 2011 May 17.

Abstract

Healthy adults aged ≥ 70 years (N=443) with no history of pneumococcal vaccination received 7- or 9-valent pneumococcal conjugate vaccine (PCV7 or PCV9) at 1 × (PCV7 only), 2 × (PCV7+PCV9), or 4 × (2 × PCV7+2 × PCV9) dosage in a randomised, open-label study evaluating pneumococcal protein conjugate vaccine (PnC). Controls received 23-valent pneumococcal polysaccharide vaccine (PPV). Both geometric mean concentration enzyme-linked immunosorbent assay and opsonophagocytic activity antibody titres assessed 1 month after vaccination were significantly increased over baseline titres for all PCV7 serotypes, with a trend toward a dose-dependent immune response. Local reactions for the 4 × dose, but not the 2 × dose, were statistically significantly higher than for the 1 × dose. No treatment-related serious adverse events occurred.

摘要

在一项评估肺炎球菌蛋白结合疫苗(PnC)的随机、开放性研究中,443 名无肺炎球菌疫苗接种史的健康成年人(年龄≥70 岁,N=443)接受了 7 价或 9 价肺炎球菌结合疫苗(PCV7 或 PCV9)1 剂(仅 PCV7)、2 剂(PCV7+PCV9)或 4 剂(2 剂 PCV7+2 剂 PCV9)的接种。对照组接种 23 价肺炎球菌多糖疫苗(PPV)。所有 PCV7 血清型的酶联免疫吸附测定和调理吞噬活性抗体滴度在接种后 1 个月均较基线滴度显著升高,且呈剂量依赖性免疫应答趋势。4 剂组的局部反应(而非 2 剂组)明显高于 1 剂组。未发生与治疗相关的严重不良事件。

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