Department of Biochemistry, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Plant Biotechnol J. 2015 Oct;13(8):1056-70. doi: 10.1111/pbi.12471. Epub 2015 Sep 7.
Although the plant-made vaccine field started three decades ago with the promise of developing low-cost vaccines to prevent infectious disease outbreaks and epidemics around the globe, this goal has not yet been achieved. Plants offer several major advantages in vaccine generation, including low-cost production by eliminating expensive fermentation and purification systems, sterile delivery and cold storage/transportation. Most importantly, oral vaccination using plant-made antigens confers both mucosal (IgA) and systemic (IgG) immunity. Studies in the past 5 years have made significant progress in expressing vaccine antigens in edible leaves (especially lettuce), processing leaves or seeds through lyophilization and achieving antigen stability and efficacy after prolonged storage at ambient temperatures. Bioencapsulation of antigens in plant cells protects them from the digestive system; the fusion of antigens to transmucosal carriers enhances efficiency of their delivery to the immune system and facilitates successful development of plant vaccines as oral boosters. However, the lack of oral priming approaches diminishes these advantages because purified antigens, cold storage/transportation and limited shelf life are still major challenges for priming with adjuvants and for antigen delivery by injection. Yet another challenge is the risk of inducing tolerance without priming the host immune system. Therefore, mechanistic aspects of these two opposing processes (antibody production or suppression) are discussed in this review. In addition, we summarize recent progress made in oral delivery of vaccine antigens expressed in plant cells via the chloroplast or nuclear genomes and potential challenges in achieving immunity against infectious diseases using cold-chain-free vaccine delivery approaches.
尽管植物制造疫苗领域在三十年前就已经起步,承诺开发低成本疫苗以预防全球范围内的传染病爆发和流行,但这一目标尚未实现。植物在疫苗生产方面具有几个主要优势,包括通过消除昂贵的发酵和纯化系统来实现低成本生产、无菌输送和冷藏/运输。最重要的是,使用植物制造的抗原进行口服接种可同时产生黏膜(IgA)和系统(IgG)免疫。过去 5 年的研究在表达疫苗抗原方面取得了重大进展,可将抗原表达在可食用的叶片(尤其是生菜)中,通过冷冻干燥处理叶片或种子,并在常温下长时间储存后保持抗原的稳定性和功效。将抗原生物封装在植物细胞中可保护它们免受消化系统的影响;将抗原融合到黏膜载体上可提高其向免疫系统传递的效率,并促进植物疫苗作为口服增强剂的成功开发。然而,缺乏口服启动方法削弱了这些优势,因为纯化抗原、冷藏/运输和有限的保质期仍然是用佐剂进行启动以及通过注射进行抗原传递的主要挑战。另一个挑战是在不启动宿主免疫系统的情况下诱导耐受的风险。因此,本文讨论了这两个相反过程(抗体产生或抑制)的机制方面。此外,我们总结了最近在通过叶绿体或核基因组表达植物细胞中的疫苗抗原的口服传递方面取得的进展,以及在使用无冷链疫苗传递方法实现针对传染病的免疫方面的潜在挑战。