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基于腺病毒载体的流感黏膜疫苗的研制。

Development of adenoviral vector-based mucosal vaccine against influenza.

机构信息

Laboratory of Molecular Biotechnology, Gamaleya Research Institute of Epidemiology and Microbiology, ul. Gamaleya 18, Moscow 123098, Russia.

出版信息

J Mol Med (Berl). 2011 Apr;89(4):331-41. doi: 10.1007/s00109-010-0696-0. Epub 2010 Nov 21.

Abstract

The recent pandemic threat of the influenza virus makes the increased safety and efficiency of vaccination against the pathogen a most important issue. It has been well established that for maximum protective effect, the vaccination should mimic natural infection. Therefore, recent efforts to develop a new influenza vaccine have focused on intranasal immunization strategies. Intranasal immunization is capable of inducing secretory IgA and serum IgG responses to provide a double defense against mucosal pathogens. On the other hand, it is desirable that a live pathogen is not present in the vaccine. In addition, for optimal induction of the immune responses via the nasal route, efficient and safe mucosal adjuvants are also required. This is possible to attain using an adenoviral vector for vaccine development. Adenoviral vectors are capable of delivering and protecting the antigen encoding sequence. They also possess a natural mechanism for penetrating into the nasal mucous membrane and are capable of activating the innate immune response. This review describes the basic prerequisites for the involvement of recombinant adenoviruses for mucosal (nasal) vaccine development against the influenza virus.

摘要

流感病毒最近的流行威胁使得增加针对病原体的疫苗接种的安全性和效率成为最重要的问题。已经充分确立,为了获得最大的保护效果,疫苗接种应该模拟自然感染。因此,最近开发新流感疫苗的努力集中在鼻内免疫策略上。鼻内免疫能够诱导分泌型 IgA 和血清 IgG 反应,提供针对粘膜病原体的双重防御。另一方面,理想情况下疫苗中不应存在活病原体。此外,为了通过鼻腔途径最佳地诱导免疫反应,还需要高效和安全的粘膜佐剂。这可以使用腺病毒载体来实现疫苗开发。腺病毒载体能够传递和保护编码抗原的序列。它们还具有穿透鼻黏膜的天然机制,并能够激活先天免疫反应。本文综述了重组腺病毒参与针对流感病毒的粘膜(鼻内)疫苗开发的基本前提条件。

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