Suppr超能文献

携带HIV-1MN env基因的非复制型、宿主范围受限的金丝雀痘病毒载体(ALVAC)在血清阴性成年人中诱导1型人类免疫缺陷病毒(HIV-1)特异性细胞溶解T淋巴细胞反应。

Induction of human immunodeficiency virus type 1 (HIV-1)-specific cytolytic T lymphocyte responses in seronegative adults by a nonreplicating, host-range-restricted canarypox vector (ALVAC) carrying the HIV-1MN env gene.

作者信息

Egan M A, Pavlat W A, Tartaglia J, Paoletti E, Weinhold K J, Clements M L, Siliciano R F

机构信息

Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

J Infect Dis. 1995 Jun;171(6):1623-7. doi: 10.1093/infdis/171.6.1623.

Abstract

CD8+ cytolytic T lymphocytes (CTL) are likely to be an important component of effective vaccines against human immunodeficiency virus type 1 (HIV-1). CTL can be induced most effectively with live virus vectors. However, because of concerns about the safety of such vectors, a nonreplicating canarypox vector (ALVAC) capable of expressing foreign genes in mammalian cells has been developed. This study evaluated the capacity of an ALVAC vector expressing the HIV-1MN envelope (env) glycoprotein to induce HIV-1-specific CTL in seronegative volunteers. Protocols were designed to determine whether immunization with ALVAC alone or in combination with subunit boosting could induce CTL in vaccinia-immune and -naive volunteers. A simple method for antigen-specific in vitro stimulation was used to detect CTL responses in HIV-1-seronegative vaccine recipients. The results indicate that low doses of a nonreplicating virus vector alone can elicit both CD4+ and CD8+ HIV-1-specific CTL in a subset of seronegative volunteers.

摘要

CD8 + 细胞毒性T淋巴细胞(CTL)可能是抗1型人类免疫缺陷病毒(HIV - 1)有效疫苗的重要组成部分。活病毒载体能最有效地诱导CTL。然而,由于担心此类载体的安全性,已开发出一种能够在哺乳动物细胞中表达外源基因的非复制型金丝雀痘病毒载体(ALVAC)。本研究评估了表达HIV - 1MN包膜(env)糖蛋白的ALVAC载体在血清阴性志愿者中诱导HIV - 1特异性CTL的能力。设计方案以确定单独使用ALVAC免疫或与亚单位加强免疫联合使用是否能在接种过痘苗和未接种过痘苗的志愿者中诱导CTL。一种简单的抗原特异性体外刺激方法用于检测HIV - 1血清阴性疫苗接种者的CTL反应。结果表明,低剂量的非复制型病毒载体单独即可在一部分血清阴性志愿者中引发CD4 + 和CD8 + HIV - 1特异性CTL。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验