Design and construction of T-lymphocyte epitope-based therapeutic HIV-1 vaccines

Mark J Newman , Dennis McKinney , Robert Chesnut , Alessandro Sette , Cara Wilson , Brian Livingston
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引用次数: 0

Abstract

The demonstration that highly active anti-retroviral therapy (HAART) can control human immunodeficiency virus type 1 (HIV-1) viral replication and the associated destruction of the immune system provides an opportunity to implement therapeutic vaccine strategies. The Epimmune approach is based on separate vaccine immunogens designed to induce, or augment, helper T-lymphocyte (HTL) or cytotoxic T-lymphocyte (CTL) responsiveness when administered in conjunction with HAART. The vaccines are composed of carefully selected, minimal HTL or CTL epitopes. Vaccines composed of multiple epitopes can be produced and delivered using different formats, including deoxyribonucleic acid (DNA) plasmid-based vaccines and recombinant proteins.

基于t淋巴细胞表位的治疗性HIV-1疫苗的设计与构建
高活性抗逆转录病毒疗法(HAART)可以控制人类免疫缺陷病毒1型(HIV-1)病毒的复制和相关的免疫系统破坏,这一证明为实施治疗性疫苗策略提供了机会。Epimmune方法是基于单独的疫苗免疫原,设计用于诱导或增强辅助t淋巴细胞(HTL)或细胞毒性t淋巴细胞(CTL)与HAART联合使用时的反应性。疫苗由精心挑选的最小HTL或CTL表位组成。由多个表位组成的疫苗可以以不同的形式生产和递送,包括基于脱氧核糖核酸(DNA)质粒的疫苗和重组蛋白。
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