Laboratory of Immunotherapy, Oncology Division, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Icon Genetics GmbH, Halle, Germany.
Ann Oncol. 2010 Dec;21(12):2420-2427. doi: 10.1093/annonc/mdq256. Epub 2010 May 21.
Animal and clinical studies with plant-produced single-chain variable fragment lymphoma vaccines have demonstrated specific immunogenicity and safety. However, the expression levels of such fragments were highly variable and required complex engineering of the linkers. Moreover, the downstream processing could not be built around standard methods like protein A affinity capture.
We report a novel vaccine manufacturing process, magnifection, devoid of the above-mentioned shortcomings and allowing consistent and efficient expression in plants of whole immunoglobulins (Igs).
Full idiotype (Id)-containing IgG molecules of 20 lymphoma patients and 2 mouse lymphoma models were expressed at levels between 0.5 and 4.8 g/kg of leaf biomass. Protein A affinity capture purification yielded antigens of pharmaceutical purity. Several patient Igs produced in plants showed specific cross-reactivity with sera derived from the same patients immunized with hybridoma-produced Id vaccine. Mice vaccinated with plant- or hybridoma-produced Igs showed comparable protection levels in tumor challenge studies.
This manufacturing process is reliable and robust, the manufacturing time from biopsy to vaccine is <12 weeks and the expression and purification of antigens require only 2 weeks. The process is also broadly applicable for manufacturing monoclonal antibodies in plants, providing 50- to 1000-fold higher yields than alternative plant expression methods.
动物和临床研究表明,植物生产的单链可变片段淋巴瘤疫苗具有特异性免疫原性和安全性。然而,这些片段的表达水平高度可变,需要对连接子进行复杂的工程改造。此外,下游处理不能围绕像蛋白 A 亲和捕获这样的标准方法构建。
我们报告了一种新型疫苗制造工艺,称为 magnifection,它没有上述缺点,可以在植物中一致且高效地表达完整的免疫球蛋白(Ig)。
20 名淋巴瘤患者和 2 种小鼠淋巴瘤模型的完整独特型(Id)包含的 IgG 分子在 0.5 至 4.8 g/kg 叶生物质的水平上表达。蛋白 A 亲和捕获纯化得到了具有药物纯度的抗原。从植物中产生的几种患者 Ig 与用杂交瘤产生的 Id 疫苗免疫的相同患者的血清显示出特异性交叉反应性。在肿瘤挑战研究中,用植物或杂交瘤产生的 Ig 接种的小鼠显示出可比的保护水平。
该制造工艺可靠且稳健,从活检到疫苗的制造时间<12 周,抗原的表达和纯化仅需 2 周。该工艺还广泛适用于植物中制造单克隆抗体,提供比替代植物表达方法高 50 至 1000 倍的产量。