Karasev Alexander V, Foulke Scott, Wellens Candice, Rich Amy, Shon Kyu J, Zwierzynski Izabela, Hone David, Koprowski Hilary, Reitz Marvin
Biotechnology Foundation Laboratories at Thomas Jefferson University, Department of Microbiology and Immunology, 700 E. Butler Avenue, Doylestown, PA 18901, USA.
Vaccine. 2005 Mar 7;23(15):1875-80. doi: 10.1016/j.vaccine.2004.11.021.
The HIV-1 Tat protein has been recently explored as a prospective vaccine candidate with broad, subtype non-specific action. We approached the problem of delivery of Tat through the mucosal route by expressing Tat in an edible plant. The tat gene was assembled from synthetic overlapping oligonucleotides, and was subsequently cloned into a plant virus-based vector tobacco mosaic virus (TMV). Spinach plants inoculated with the Tat-producing constructs were collected and fed to mice 7-14 days post inoculation. DNA vaccinations were performed using a gene gun. Codon optimization of the Tat gene expressed in spinach plants resulted in several-fold yield increase as detected in immunoblots, and did not cause severe symptoms in inoculated plants. Mice were fed with the Tat-producing or control vector-inoculated spinach. After three feedings, 1 week apart, 1g per mice, no differences were detected in the growth rate or behavior of the animals fed with these three types of spinach. None of the animals developed measurable Tat antibodies. Following DNA vaccination, however, mice having previously received oral Tat developed higher antibody titers to Tat than did the controls, with the titers peaking at 4 weeks post-vaccination. Codon optimization allows production of up to 300-500 microg of Tat antigen per 1 g of leaf tissue in spinach using a plant virus-based expression system. The plant produced Tat does not seem to have any apparent adverse effect on mice growth or behavior, when fed with spinach for 4 weeks. ELISA data suggested that oral Tat primed for the development of Tat antibodies when mice were subsequently vaccinated with plasmid DNA designed for Tat expression.
HIV-1反式激活因子(Tat蛋白)最近被作为一种具有广泛、亚型非特异性作用的潜在疫苗候选物进行研究。我们通过在可食用植物中表达Tat蛋白来解决经黏膜途径递送Tat蛋白的问题。tat基因由合成的重叠寡核苷酸组装而成,随后被克隆到基于植物病毒的烟草花叶病毒(TMV)载体中。接种了产生Tat蛋白构建体的菠菜植株在接种后7 - 14天被收集并喂给小鼠。使用基因枪进行DNA疫苗接种。菠菜植株中表达的Tat基因的密码子优化导致免疫印迹检测到的产量增加了几倍,并且对接种的植株没有造成严重症状。给小鼠喂食产生Tat蛋白或接种对照载体的菠菜。每隔1周进行三次喂食,每次每只小鼠1克,结果发现喂食这三种菠菜的小鼠在生长速度或行为上没有差异。所有动物均未产生可检测到的Tat抗体。然而,在进行DNA疫苗接种后,之前口服过Tat蛋白的小鼠产生的针对Tat蛋白的抗体滴度高于对照组,抗体滴度在接种后4周达到峰值。使用基于植物病毒的表达系统,密码子优化可使菠菜每1克叶片组织产生高达300 - 500微克的Tat抗原。当给小鼠喂食菠菜4周时发现,植物产生的Tat蛋白似乎对小鼠生长或行为没有任何明显的不良影响。酶联免疫吸附测定(ELISA)数据表明,当小鼠随后接种用于表达Tat蛋白的质粒DNA时,口服Tat蛋白可引发Tat抗体的产生。