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用于疫苗生产和基因治疗的甲病毒载体。

Alphavirus vectors for vaccine production and gene therapy.

作者信息

Lundstrom Kenneth

机构信息

Regulon Inc., Epalinges, Switzerland.

出版信息

Expert Rev Vaccines. 2003 Jun;2(3):447-59. doi: 10.1586/14760584.2.3.445.

Abstract

Alphavirus vectors demonstrate high expression of heterologous proteins in a broad range of host cells. Replication-deficient as well as replication-competent variants exist. Systemic delivery of many viral antigens has elicited strong antibody responses in immunized mice and primates, and protection against challenges with lethal viruses was obtained. Similarly, prophylactic vaccination was established against tumor challenges. Attention has been paid to the engineering of improved targeting to immunologically active cells, such as dendritic cells. In the area of gene therapy, intratumoral injections of alphavirus vectors have resulted in potentially promising tumor rejection. Moreover, encapsulation of alphavirus particles into liposomes demonstrated efficient tumor targeting in mice with severe combined immunodeficiency, which permitted the initiation of clinical trials for patients with advanced kidney carcinoma and melanoma.

摘要

甲病毒载体在广泛的宿主细胞中能高效表达异源蛋白。存在复制缺陷型以及复制 competent 型变体。多种病毒抗原的全身递送已在免疫小鼠和灵长类动物中引发强烈的抗体反应,并获得了针对致死性病毒攻击的保护作用。同样,也建立了针对肿瘤攻击的预防性疫苗接种。人们已关注到改进靶向免疫活性细胞(如树突状细胞)的工程设计。在基因治疗领域,瘤内注射甲病毒载体已导致具有潜在前景的肿瘤排斥反应。此外,将甲病毒颗粒包裹在脂质体中在严重联合免疫缺陷小鼠中显示出高效的肿瘤靶向性,这使得针对晚期肾癌和黑色素瘤患者的临床试验得以启动。

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