From the Clinical Sciences, Sanofi Pasteur, Mexico City, Mexico.
Endowed Health Services Research Center, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico.
Pediatr Infect Dis J. 2020 Oct;39(10):961-968. doi: 10.1097/INF.0000000000002830.
We previously described an increased immune response 28 days after a booster dose of the live, attenuated, tetravalent dengue vaccine (CYD-TDV) in healthy adolescents and adults in Latin America (CYD64, NCT02623725). This follow-up study evaluated immune response persistence and safety of a CYD-TDV booster dose up to Month (M) 24 post-booster.
This study included 250 participants who previously received 3 primary doses of CYD-TDV in the CYD13 (NCT00993447) and CYD30 (NCT01187433) studies, and who were randomized 4-5 years later to receive a CYD-TDV booster or placebo (3:1). Dengue neutralizing antibodies against the parental dengue virus strains were assessed using the plaque reduction neutralization test (PRNT50) at M6, M12, and M24 post-booster. Post-booster memory B-cell responses were assessed in a subset of participants using the FluoroSpot assay up to M12 post-booster.
In the CYD-TDV group (n = 187), dengue neutralizing antibody geometric mean titers (GMTs) declined from the peak at day 28 through to M24 for all serotypes. GMTs at M24 were similar to those at pre-booster among baseline dengue seropositives. A similar trend was observed for baseline dengue seronegatives, albeit at a lower magnitude. Previous vaccination-induced detectable B-cell memory responses in seropositives and seronegatives that decreased to pre-booster levels at M12 post-booster. The CYD-TDV booster dose was well-tolerated.
In baseline dengue seropositives, following a CYD-TDV booster dose administered 4-5 years after primary immunization, dengue neutralizing antibody GMTs and B-cell memory responses peaked in the short-term before gradually decreasing over time. A CYD-TDV booster dose could improve protection against dengue during outbreak periods.
我们之前描述过,在拉丁美洲健康的青少年和成年人中,活的、减毒的、四价登革热疫苗(CYD-TDV)加强剂量会在 28 天后引发更强的免疫反应(CYD64,NCT02623725)。这项随访研究评估了 CYD-TDV 加强剂量在加强后 24 个月(M)内的免疫反应持久性和安全性。
这项研究纳入了 250 名参与者,他们之前在 CYD13(NCT00993447)和 CYD30(NCT01187433)研究中接受了 3 次基础剂量的 CYD-TDV,4-5 年后随机接受 CYD-TDV 加强剂量或安慰剂(3:1)。在加强后 M6、M12 和 M24,使用蚀斑减少中和试验(PRNT50)评估针对亲本登革热病毒株的登革热中和抗体。在加强后至 M12,通过 FluoroSpot 检测评估一部分参与者的记忆 B 细胞反应。
在 CYD-TDV 组(n=187),所有血清型的登革热中和抗体几何平均滴度(GMT)从第 28 天的峰值下降到 M24。在基线登革热血清阳性者中,M24 的 GMT 与加强前相似。在基线登革热血清阴性者中也观察到了类似的趋势,尽管幅度较小。以前的疫苗接种在血清阳性者和血清阴性者中诱导了可检测到的 B 细胞记忆反应,这些反应在加强后 12 个月时下降到加强前的水平。CYD-TDV 加强剂量的耐受性良好。
在基线登革热血清阳性者中,在初次免疫后 4-5 年接种 CYD-TDV 加强剂量后,登革热中和抗体 GMT 和 B 细胞记忆反应在短期内达到峰值,然后随着时间的推移逐渐下降。接种 CYD-TDV 加强剂量可能会在登革热爆发期间改善对登革热的保护。