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登革热和 Zika 病毒的免疫反应——T 细胞疫苗开发指南。

Immune Responses to Dengue and Zika Viruses-Guidance for T Cell Vaccine Development.

机构信息

Functional Genetics of Infectious Diseases Unit, Institut Pasteur, 75015 Paris, France.

CNRS UMR 2000-Génomique Évolutive, Modélisation et Santé, Institut Pasteur, 75015 Paris, France.

出版信息

Int J Environ Res Public Health. 2018 Feb 23;15(2):385. doi: 10.3390/ijerph15020385.

Abstract

Despite numerous efforts to identify the molecular and cellular effectors of the adaptive immunity that induce a long-lasting immunity against dengue or Zika virus infection, the specific mechanisms underlying such protective immunity remain largely unknown. One of the major challenges lies in the high level of dengue virus (DENV) seroprevalence in areas where Zika virus (ZIKV) is circulating. In the context of such a pre-existing DENV immunity that can exacerbate ZIKV infection and disease, and given the lack of appropriate treatment for ZIKV infection, there is an urgent need to develop an efficient vaccine against DENV and ZIKV. Notably, whereas several ZIKV vaccine candidates are currently in clinical trials, all these vaccine candidates have been designed to induce neutralizing antibodies as the primary mechanism of immune protection. Given the difficulty to elicit simultaneously high levels of neutralizing antibodies against the different DENV serotypes, and the potential impact of pre-existing subneutralizing antibodies induced upon DENV infection or vaccination on ZIKV infection and disease, additional or alternative strategies to enhance vaccine efficacy, through T cell immunity, are now being considered. In this review, we summarize recent discoveries about cross-reactive B and T cell responses against DENV and ZIKV and propose guidelines for the development of safe and efficient T cell vaccines targeting both viruses.

摘要

尽管人们已经做出了许多努力来寻找引发针对登革热或寨卡病毒感染的长期免疫的适应性免疫的分子和细胞效应物,但这种保护性免疫的具体机制在很大程度上仍然未知。其中一个主要挑战在于在寨卡病毒(ZIKV)流行的地区,登革热病毒(DENV)的血清阳性率很高。在这种已经存在的 DENV 免疫可能会加剧 ZIKV 感染和疾病的情况下,并且由于缺乏针对 ZIKV 感染的适当治疗方法,因此迫切需要开发针对 DENV 和 ZIKV 的有效疫苗。值得注意的是,尽管目前有几种寨卡病毒疫苗候选物正在临床试验中,但所有这些疫苗候选物的设计都是为了诱导中和抗体作为免疫保护的主要机制。鉴于难以同时针对不同的 DENV 血清型产生高水平的中和抗体,并且在 DENV 感染或接种疫苗后预先存在的亚中和抗体可能会对 ZIKV 感染和疾病产生影响,因此现在正在考虑通过 T 细胞免疫来增强疫苗效力的其他或替代策略。在这篇综述中,我们总结了最近关于针对 DENV 和 ZIKV 的交叉反应性 B 和 T 细胞反应的发现,并提出了针对这两种病毒的安全有效的 T 细胞疫苗的开发指南。

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