Wang B, Merva M, Dang K, Ugen K E, Boyer J, Williams W V, Weiner D B
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
AIDS Res Hum Retroviruses. 1994;10 Suppl 2:S35-41.
Direct DNA inoculation induces immune responses through the delivery of nonreplicating transcription units that drive the synthesis of specific foreign proteins within the inoculated host. These proteins are processed within host cells and through association with relevant MHC antigens that can become the subject of immune surveillance and elicit immune responses against pathogens. Direct introduction of DNA into mice has been reported to be antigenic as demonstrated by the use of this technique to develop immune responses against human growth hormone, influenza proteins, as well as HIV-1 proteins. Most recently the demonstration of the use of this technology to produce anti-HIV-1 immune responses has been reported in nonhuman primates. Accordingly a more detailed analysis of this technology could generate important insight into the generality of this approach for immune therapy or vaccine design. In this article we further our investigation of direct DNA inoculation as a tool for induction of relevant immune responses against HIV-1 in vivo. We demonstrate expression of HIV-1 antigens in the inoculated muscle of animals. Inoculated animals demonstrate significant cytotoxic T cell responses against HIV-1 antigen-expressing targets. Furthermore, using a novel challenge system, we demonstrate that the majority of immunized animals can reject lethal, HIV-1 antigen-expressing cell challenge in an antigen-specific manner. This technology has relevance for the development of immunization strategies against HIV as it provides for specific antigen production in vivo without the use of infectious agents.
直接DNA接种通过传递非复制性转录单位来诱导免疫反应,这些转录单位驱动接种宿主内特定外源蛋白的合成。这些蛋白在宿主细胞内被加工,并与相关的MHC抗原结合,从而成为免疫监视的对象并引发针对病原体的免疫反应。据报道,将DNA直接导入小鼠具有抗原性,使用该技术针对人生长激素、流感蛋白以及HIV-1蛋白产生免疫反应就证明了这一点。最近,在非人类灵长类动物中报道了使用该技术产生抗HIV-1免疫反应的情况。因此,对该技术进行更详细的分析可能会为这种免疫治疗或疫苗设计方法的普遍性提供重要见解。在本文中,我们进一步研究直接DNA接种作为在体内诱导针对HIV-1的相关免疫反应的工具。我们证明了HIV-1抗原在接种动物的肌肉中的表达。接种动物表现出针对表达HIV-1抗原的靶标的显著细胞毒性T细胞反应。此外,使用一种新型攻击系统,我们证明大多数免疫动物能够以抗原特异性方式排斥致命的、表达HIV-1抗原的细胞攻击。这项技术与抗HIV免疫策略的发展相关,因为它无需使用感染性因子就能在体内产生特异性抗原。