Safety and Immunogenicity of the Live-Attenuated Quadrivalent Dengue Vaccine V181 Compared With Butantan-DV Among Healthy Adults in Brazil: A Randomized, Double-Blind, Phase 2 Trial.

IF 8.3 1区 医学 Q1 IMMUNOLOGY
David Alexanderian, Fabiano Ramos, Soumya Chatterjee, Alexandre Vargas Schwarzbold, Ana Paula Loch, Ariane Cristina Barboza Zanetti, Qiuxu Chen, Jason Martin, Matthew T Onorato, Germán Áñez
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引用次数: 0

Abstract

Background: Dengue is caused by infection with 1 of 4 dengue virus (DENV) serotypes (DENV-1 to DENV-4). V181 and Butantan-Dengue Vaccine (Butantan-DV) are independently developed, single-dose, quadrivalent dengue vaccines based on the same attenuated parental strains.

Methods: In this randomized, double-blind, active comparator-controlled, multisite, phase 2 trial, we compared the safety and immunogenicity of V181 and Butantan-DV in healthy adults in Brazil. The primary immunogenicity objectives were to compare vaccine-induced neutralizing antibody geometric mean titers (GMTs) and seroconversion rates for DENV-1 to DENV-4 at day 28 postvaccination. The primary and secondary safety objectives, respectively, were to assess vaccine-related serious adverse events and the proportion of participants experiencing solicited adverse events through day 28 postvaccination.

Results: Overall, 1364 participants were assigned (1:1) to receive V181 (n = 682) or Butantan-DV (n = 682). At day 28 postvaccination, V181 induced a noninferior immune response to Butantan-DV for DENV-1 and DENV-2 but not DENV-3 and DENV-4, as measured using GMT ratios. Noninferiority was established for all DENV serotypes based on seroconversion rates. Most participants developed a trivalent or tetravalent neutralizing antibody response. Vaccine viremia was detected for each DENV serotype. V181 and Butantan-DV were generally well tolerated.

Conclusions: V181 was immunogenic in adults, and while immunogenicity was noninferior to Butantan-DV for DENV-1 and DENV-2, seroconversion rates were noninferior for DENV-1 to DENV-4. The safety profile of V181 is comparable to that of Butantan-DV and supports its continued evaluation as a single-dose quadrivalent vaccine for dengue prevention.

Clinical trials registration: NCT05710224.

四价登革热减毒活疫苗V181与Butantan-DV在巴西健康成人中的安全性和免疫原性:一项随机、双盲、2期试验
背景:登革热是由四种登革热病毒(DENV)血清型(DENV-1至DENV-4)中的一种感染引起的。V181和butantan -登革热疫苗(Butantan-DV)是独立开发的单剂量四价登革热疫苗,基于相同的减毒亲本菌株。方法:在这项随机、双盲、主动对照、多位点、2期试验中,我们比较了V181和Butantan-DV在巴西健康成人中的安全性和免疫原性。主要的免疫原性目标是比较疫苗诱导的中和抗体几何平均滴度(GMTs)和DENV-1到DENV-4在接种后第28天的血清转化率。主要和次要安全性目标分别是评估疫苗相关的严重不良事件以及在接种后第28天经历征求性不良事件的参与者比例。结果:总体而言,1364名参与者被分配(1:1)接受V181 (n = 682)或Butantan-DV (n = 682)。接种后第28天,V181诱导buantan - dv对DENV-1和DENV-2的非劣势免疫应答,但对DENV-3和DENV-4的非劣势免疫应答。基于血清转化率,所有DENV血清型均建立了非劣效性。大多数参与者产生了三价或四价中和抗体反应。每种DENV血清型均检测到疫苗病毒血症。V181和buantan - dv一般耐受良好。结论:V181在成人中具有免疫原性,虽然DENV-1和DENV-2的免疫原性不逊于Butantan-DV,但DENV-1到DENV-4的血清转化率也不逊于Butantan-DV。V181的安全性与Butantan-DV相当,并支持其作为预防登革热的单剂量四价疫苗的持续评估。临床试验注册:NCT05710224。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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