Haynes J R, McCabe D E, Swain W F, Widera G, Fuller J T
Agracetus, Inc., Middleton, WI 53562, USA.
J Biotechnol. 1996 Jan 26;44(1-3):37-42. doi: 10.1016/0168-1656(96)80298-7.
Nucleic acid immunization involves the direct in vivo administration of antigen-encoding plasmid DNA molecules that results in the de novo production of correctly folded microbial antigens at the site of DNA delivery. While this process can lead to the development of neutralizing antibody responses recognizing authentic protein conformations, in vivo antigen production also results in epitope presentation via the MHC class I antigen processing pathway, leading to the elicitation of cytotoxic cellular immune responses. Recent efforts in the authors' laboratories have focused on use of the Accell gene delivery system (gene gun) to achieve the direct, intracellular delivery of small quantities of DNA into cells of the epidermis. The gene gun approach to nucleic acid vaccination capitalizes on the synergistic combination of an effective DNA delivery system and a target tissue that serves as a major immunological inductive site. Experimental gene gun-based nucleic acid vaccines can achieve potent humoral and cytotoxic cellular immune responses in rodent models following immunization with as little as 16 ng of DNA. Equally strong responses have also been elicited in larger animals, such as pigs and monkeys, following epidermal immunization with as little as 2 to 4 micrograms of DNA.
核酸免疫涉及直接在体内施用编码抗原的质粒DNA分子,这会导致在DNA递送部位从头产生正确折叠的微生物抗原。虽然这个过程可以引发识别真实蛋白质构象的中和抗体反应,但体内抗原的产生也会通过MHC I类抗原加工途径导致表位呈递,从而引发细胞毒性细胞免疫反应。作者实验室最近的工作重点是使用Accell基因递送系统(基因枪),将少量DNA直接细胞内递送至表皮细胞。基因枪核酸疫苗接种方法利用了有效的DNA递送系统与作为主要免疫诱导部位的靶组织之间的协同组合。在啮齿动物模型中,基于基因枪的实验性核酸疫苗在用低至16 ng DNA免疫后可产生强效的体液和细胞毒性细胞免疫反应。在用低至2至4微克DNA进行表皮免疫后,在诸如猪和猴等大型动物中也引发了同样强烈的反应。