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A组链球菌疫苗研发的现状

Current status of group A streptococcal vaccine development.

作者信息

Dale James B

机构信息

University of Tennessee Health Science Center, Memphis 38104, USA.

出版信息

Adv Exp Med Biol. 2008;609:53-63. doi: 10.1007/978-0-387-73960-1_5.

Abstract

We now have a much more detailed understanding of the molecular pathogenesis of GAS infections. These discoveries have led to the identification of several vaccine candidates which are in various stages of development. One of the leading candidate antigens is the surface M protein, which confers protection against infection in animal models. In addition, M antibodies in human serum correlate with protection against infection with the homologous serotype of GAS. Molecular techniques have been used to genetically engineer highly complex multivalent M protein-based vaccines that appear to be free of potentially harmful tissue crossreactive epitopes. A 26-valent vaccine has been shown to be well-tolerated and immunogenic in adult volunteers and is now being considered for pediatric trials, which is the primary target group for the vaccine. Ongoing efforts are now addressing the epidemiology of GAS infections in developing countries so that new vaccines can be designed to prevent the infections that may trigger ARF and RHD. Successful deployment of safe and effective vaccines to prevent GAS infections and their complications could potentially have a significant impact on the health of millions of people around the world.

摘要

我们现在对A群链球菌(GAS)感染的分子发病机制有了更为详细的了解。这些发现促成了几种处于不同开发阶段的候选疫苗的识别。主要候选抗原之一是表面M蛋白,它在动物模型中可提供抗感染保护。此外,人血清中的M抗体与针对同源血清型GAS感染的保护作用相关。分子技术已被用于基因工程改造高度复杂的多价M蛋白疫苗,这些疫苗似乎没有潜在有害的组织交叉反应表位。一种26价疫苗已在成年志愿者中显示出耐受性良好且具有免疫原性,目前正在考虑进行儿科试验,而儿童是该疫苗的主要目标群体。目前正在持续努力研究发展中国家GAS感染的流行病学,以便设计新的疫苗来预防可能引发急性风湿热(ARF)和风湿性心脏病(RHD)的感染。成功部署安全有效的疫苗以预防GAS感染及其并发症可能会对全球数百万人的健康产生重大影响。

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