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进展与展望:病毒载体的免疫反应。

Progress and prospects: immune responses to viral vectors.

机构信息

Department Pediatrics, University of Florida, Gainesville, FL 32610, USA.

出版信息

Gene Ther. 2010 Mar;17(3):295-304. doi: 10.1038/gt.2009.148. Epub 2009 Nov 12.

Abstract

Viral vectors are potent gene delivery platforms used for the treatment of genetic and acquired diseases. However, just as viruses have evolved to infect cells efficiently, the immune system has evolved to fight off what it perceives as invading pathogens. Therefore, innate immunity and antigen-specific adaptive immune responses against vector-derived antigens reduce the efficacy and stability of in vivo gene transfer. In addition, a number of vectors are derived from parent viruses that humans encounter through natural infection, resulting in preexisting antibodies and possibly in memory responses against vector antigens. Similarly, antibody and T-cell responses may be directed against therapeutic gene products that often differ from the endogenous nonfunctional or absent protein that is being replaced. As details and mechanisms of such immune reactions are uncovered, novel strategies are being developed, and vectors are being specifically engineered to avoid, suppress or manipulate the response, ideally resulting in sustained expression and immune tolerance to the transgene product. This review provides a summary of our current knowledge of the interactions between the immune system adeno-associated virus, adenoviral and lentiviral vectors, and their transgene products.

摘要

病毒载体是用于治疗遗传和获得性疾病的有效基因传递平台。然而,正如病毒已经进化到能够高效感染细胞一样,免疫系统也已经进化到可以抵御它认为是入侵病原体的物质。因此,针对载体衍生抗原的固有免疫和抗原特异性适应性免疫反应降低了体内基因转移的效率和稳定性。此外,一些载体来源于人类通过自然感染接触到的亲本病毒,从而导致针对载体抗原的预先存在的抗体和可能的记忆反应。同样,抗体和 T 细胞反应可能针对治疗性基因产物,这些产物通常与正在替代的内源性无功能或缺失蛋白不同。随着对这些免疫反应的细节和机制的揭示,新的策略正在被开发出来,载体也被专门设计用来避免、抑制或操纵反应,理想情况下可以实现对转基因产物的持续表达和免疫耐受。本文综述了我们目前对免疫系统与腺相关病毒、腺病毒和慢病毒载体及其转基因产物相互作用的了解。

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