a Research & Development , Sanofi Pasteur , Marcy l'Etoile , France.
b Global Clinical Immunology Department , Sanofi Pasteur , Swiftwater , PA , USA.
Hum Vaccin Immunother. 2017 Sep 2;13(9):2004-2016. doi: 10.1080/21645515.2017.1333211. Epub 2017 Jun 9.
Two large pivotal phase III studies demonstrated the efficacy of the tetravalent dengue vaccine (CYD-TDV; Dengvaxia®, Sanofi Pasteur) against all dengue serotypes. Here we present an unprecedented integrated summary of the immunogenicity of CYD-TDV to identify the parameters driving the neutralizing humoral immune response and evolution over time. We summarized the immunogenicity profiles of a 3-dose schedule of CYD-TDV administered 6 months apart across 10 phase II and 6 phase III trials undertaken in dengue endemic and non-endemic countries. Dengue neutralizing antibody titers in sera were determined at centralized laboratories using the 50% plaque reduction neutralization test (PRNT) at baseline, 28 d after the third dose, and annually thereafter for up to 4 y after the third dose in some studies. CYD-TDV elicits neutralizing antibody responses against all 4 dengue serotypes; geometric mean titers (GMTs) increased from baseline to post-dose 3. GMTs were influenced by several parameters including age, baseline dengue seropositivity and region. In the 2 pivotal studies, GMTs decreased initially during the first 2 y post-dose 3 but appear to stabilize or slightly increase again in the third year. GMTs persisted 1.2-3.2-fold higher than baseline levels for up to 4 y post-dose 3 in other studies undertaken in dengue endemic countries. Our integrated analysis captures the fullness of the CYD-TDV immunogenicity profile across studies, age groups and regions; by presenting the available data in this way general trends and substantial outliers within each grouping can be easily identified. CYD-TDV elicits neutralizing antibody responses against all dengue serotypes, with differences by age and endemicity, which persist above baseline levels in endemic countries.
两项大型的四价登革热疫苗(CYD-TDV;Dengvaxia®,赛诺菲巴斯德)关键性 III 期研究均证明了其对所有登革热血清型的有效性。在此,我们首次对 CYD-TDV 的免疫原性进行了综合总结,以确定驱动中和抗体免疫应答的参数及其随时间的演变。我们总结了 CYD-TDV 在 10 项 II 期和 6 项 III 期研究中的免疫原性特征,这些研究在登革热流行和非流行国家进行,采用每 6 个月接种 3 剂的方案。在基线、第 3 剂后 28 天以及此后每年,在一些研究中直至第 3 剂后 4 年,在集中实验室使用 50%蚀斑减少中和试验(PRNT)测定血清中的登革热中和抗体滴度。CYD-TDV 可引发针对所有 4 种登革热血清型的中和抗体应答;GMT 从基线增加到第 3 剂后。GMT 受多种参数影响,包括年龄、基线登革热血清阳性率和地区。在两项关键研究中,GMT 在第 3 剂后 2 年内最初下降,但在第 3 年似乎稳定或再次略有增加。在其他在登革热流行国家进行的研究中,GMT 在第 3 剂后 4 年内持续保持比基线水平高 1.2-3.2 倍。我们的综合分析涵盖了跨研究、年龄组和地区的 CYD-TDV 免疫原性全貌;通过以这种方式呈现现有数据,可以轻松识别每个分组内的总体趋势和显著异常值。CYD-TDV 可引发针对所有登革热血清型的中和抗体应答,其应答存在年龄和流行程度差异,在流行国家中,这些应答持续高于基线水平。