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限制鱼类保护性黏膜疫苗设计的挑战概述

An Overview of Challenges Limiting the Design of Protective Mucosal Vaccines for Finfish.

作者信息

Munang'andu Hetron Mweemba, Mutoloki Stephen, Evensen Øystein

机构信息

Section of Aquatic Medicine and Nutrition, Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences , Oslo , Norway.

出版信息

Front Immunol. 2015 Oct 22;6:542. doi: 10.3389/fimmu.2015.00542. eCollection 2015.

Abstract

Research in mucosal vaccination in finfish has gained prominence in the last decade in pursuit of mucosal vaccines that would lengthen the duration of protective immunity in vaccinated fish. However, injectable vaccines have continued to dominate in the vaccination of finfish because they are perceived to be more protective than mucosal vaccines. Therefore, it has become important to identify the factors that limit developing protective mucosal vaccines in finfish as an overture to identifying key areas that require optimization in mucosal vaccine design. Some of the factors that limit the success for designing protective mucosal vaccines for finfish identified in this review include the lack optimized protective antigen doses for mucosal vaccines, absence of immunostimulants able to enhance the performance of non-replicative mucosal vaccines, reduction of systemic antibodies due to prolonged exposure to oral vaccination and the lack of predefined correlates of protective immunity for use in the optimization of newly developed mucosal vaccines. This review also points out the need to develop prime-boost vaccination regimes able to induce long-term protective immunity in vaccinated fish. By overcoming some of the obstacles identified herein, it is anticipated that future mucosal vaccines shall be designed to induce long-term protective immunity in finfish.

摘要

在过去十年中,为了研发能延长接种疫苗鱼类保护性免疫持续时间的黏膜疫苗,鱼类黏膜疫苗研究备受关注。然而,注射用疫苗在鱼类疫苗接种中仍占主导地位,因为人们认为它们比黏膜疫苗更具保护性。因此,确定限制鱼类保护性黏膜疫苗研发的因素变得很重要,以此作为确定黏膜疫苗设计中需要优化的关键领域的前奏。本综述中确定的一些限制鱼类保护性黏膜疫苗设计成功的因素包括:缺乏针对黏膜疫苗的优化保护性抗原剂量;缺乏能够增强非复制性黏膜疫苗性能的免疫刺激剂;由于长期口服疫苗接种导致全身抗体减少;以及缺乏用于优化新研发黏膜疫苗的预先定义的保护性免疫相关指标。本综述还指出,需要开发能够在接种疫苗的鱼类中诱导长期保护性免疫的初免 - 加强免疫接种方案。通过克服本文中确定的一些障碍,预计未来的黏膜疫苗将被设计用于在鱼类中诱导长期保护性免疫。

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