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基因治疗与病毒疫苗接种:交叉领域

Gene therapy and viral vaccination: the interface.

作者信息

Wilkinson G W, Borysiewicz L K

机构信息

Department of Medicine, University of Wales College of Medicine, Cardiff, UK.

出版信息

Br Med Bull. 1995 Jan;51(1):205-16. doi: 10.1093/oxfordjournals.bmb.a072947.

Abstract

Live viral vaccines have had a major impact on the incidence of acute virus infections world-wide. Virus infections recognised as future vaccine targets will require a modified approach based on a detailed understanding of the immunobiology of specific infections combined with the application of new technologies designed to generate specific and appropriate protective immunity. A similar vector technology directed at in vivo gene delivery is currently being exploited both for gene therapy and vaccination. The induction of an immune response to an expressed transgene represents a potential hazard for a gene therapy protocol but is the object of a vaccine strategy. In vivo gene delivery using replication-competent or replication-deficient viral vector systems and by direct transfer of naked DNA can generate an effective humoral, secretory and cell-mediated immune response to expressed transgenes.

摘要

减毒活疫苗对全球急性病毒感染的发病率产生了重大影响。被视为未来疫苗靶点的病毒感染将需要一种经过改进的方法,该方法基于对特定感染免疫生物学的详细了解,并结合旨在产生特异性和适当保护性免疫的新技术应用。一种针对体内基因递送的类似载体技术目前正被用于基因治疗和疫苗接种。对表达的转基因产生免疫反应对基因治疗方案来说是一种潜在风险,但却是疫苗策略的目标。使用具有复制能力或复制缺陷的病毒载体系统以及通过直接转移裸DNA进行体内基因递送,可以对表达的转基因产生有效的体液、分泌和细胞介导的免疫反应。

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