Current status of the development of dengue vaccines.

IF 2.7 Q3 IMMUNOLOGY
Vaccine: X Pub Date : 2024-12-17 eCollection Date: 2025-01-01 DOI:10.1016/j.jvacx.2024.100604
Michelle Felicia Lee, Chiau Ming Long, Chit Laa Poh
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引用次数: 0

Abstract

Dengue fever is caused by the mosquito-borne dengue virus (DENV), which is endemic in more than 100 countries. Annually, there are approximately 390 million dengue cases, with a small subset manifesting into severe illnesses, such as dengue haemorrhagic fever or dengue shock syndrome. Current treatment options for dengue infections remain supportive management due to the lack of an effective vaccine and clinically approved antiviral. Although the CYD-TDV (Dengvaxia®) vaccine with an overall vaccine efficacy of 60 % has been licensed for clinical use since 2015, it poses an elevated risk of severe dengue infections especially in dengue-naïve children below 9 years of age. The newly approved Qdenga vaccine was able to achieve an overall vaccine efficacy of 80 % after 12 months, but it was not able to provide a protective effect against DENV-3 in dengue naïve individuals. The Butantan-DV vaccine candidate is still undergoing phase 3 clinical trials for safety and efficacy evaluations in humans. Apart from live-attenuated vaccines, various other vaccine types are also currently being studied in preclinical and clinical studies. This review discusses the current status of dengue vaccine development.

登革热疫苗的发展现状。
登革热是由蚊媒登革热病毒(DENV)引起的,在100多个国家流行。每年约有3.9亿登革热病例,其中一小部分表现为严重疾病,如登革出血热或登革休克综合征。由于缺乏有效的疫苗和临床批准的抗病毒药物,目前登革热感染的治疗方案仍然是支持性管理。尽管总体疫苗效力为60%的CYD-TDV (Dengvaxia®)疫苗自2015年以来已获准临床使用,但它会增加严重登革热感染的风险,特别是在dengue-naïve 9岁以下儿童中。新批准的Qdenga疫苗在12个月后能够达到80%的总体疫苗效力,但它不能在登革热naïve个体中提供针对DENV-3的保护作用。Butantan-DV候选疫苗仍在进行人体安全性和有效性评估的3期临床试验。除减毒活疫苗外,目前还在临床前和临床研究中研究各种其他类型的疫苗。本文综述了登革热疫苗的研制现状。
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
Vaccine: X
Vaccine: X Multiple-
CiteScore
2.80
自引率
2.60%
发文量
102
审稿时长
13 weeks
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