Wang B, Ugen K E, Srikantan V, Agadjanyan M G, Dang K, Refaeli Y, Sato A I, Boyer J, Williams W V, Weiner D B
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4156-60. doi: 10.1073/pnas.90.9.4156.
Recently, immunization techniques in which DNA constructs are introduced directly into mammalian tissue in vivo have been developed. In theory, gene inoculation should result in the production of antigenic proteins in a natural form in the immunized host. Here we present the use of such a technique for the inoculation of mice with a human immunodeficiency virus type 1 (HIV-1) envelope DNA construct (pM160). Mice were injected intramuscularly with pM160 and were subsequently analyzed for their anti-HIV envelope immune responses. Antisera collected from inoculated animals reacted with the recombinant HIV-1 envelope in ELISA and immunoprecipitation assays. The antisera also contained antibodies that were able to neutralize HIV-1 infection and inhibit HIV-1-mediated syncytium formation in vitro. Furthermore, splenic lymphocytes derived from pM160-inoculated animals demonstrated HIV-envelope-specific proliferative responses. The gene inoculation technique mimics features of vaccination with live attenuated viruses and, therefore, may ultimately prove useful in the rapid development of safe and efficacious vaccines as it provides for production of relevant antigen in vivo without the use of infectious agents.
最近,已开发出将DNA构建体直接导入哺乳动物体内组织的免疫技术。理论上,基因接种应能使免疫宿主以天然形式产生抗原蛋白。在此,我们展示了使用这种技术用1型人类免疫缺陷病毒(HIV-1)包膜DNA构建体(pM160)接种小鼠的情况。给小鼠肌肉注射pM160,随后分析它们的抗HIV包膜免疫反应。从接种动物收集的抗血清在ELISA和免疫沉淀试验中与重组HIV-1包膜发生反应。抗血清中还含有能够在体外中和HIV-1感染并抑制HIV-1介导的合胞体形成的抗体。此外,来自接种pM160动物的脾淋巴细胞表现出HIV包膜特异性增殖反应。基因接种技术模拟了减毒活病毒疫苗接种的特点,因此,由于其能在不使用感染性因子的情况下在体内产生相关抗原,最终可能被证明对快速开发安全有效的疫苗有用。