Tusé Daniel, Ku Nora, Bendandi Maurizio, Becerra Carlos, Collins Robert, Langford Nyla, Sancho Susana Inogés, López-Díaz de Cerio Ascensión, Pastor Fernando, Kandzia Romy, Thieme Frank, Jarczowski Franziska, Krause Dieter, Ma Julian K-C, Pandya Shan, Klimyuk Victor, Gleba Yuri, Butler-Ransohoff John E
DT/Consulting Group, 2695 13th Street, Sacramento, CA 95818, USA.
DAVA Oncology LP, Two Lincoln Center, 5420 LBJ Freeway, Suite 410, Dallas, TX 75240, USA.
Biomed Res Int. 2015;2015:648143. doi: 10.1155/2015/648143. Epub 2015 Sep 6.
We report the first evaluation of plant-made conjugate vaccines for targeted treatment of B-cell follicular lymphoma (FL) in a Phase I safety and immunogenicity clinical study. Each recombinant personalized immunogen consisted of a tumor-derived, plant-produced idiotypic antibody (Ab) hybrid comprising the hypervariable regions of the tumor-associated light and heavy Ab chains, genetically grafted onto a common human IgG1 scaffold. Each immunogen was produced in Nicotiana benthamiana plants using twin magnICON vectors expressing the light and heavy chains of the idiotypic Ab. Each purified Ab was chemically linked to the carrier protein keyhole limpet hemocyanin (KLH) to form a conjugate vaccine. The vaccines were administered to FL patients over a series of ≥6 subcutaneous injections in conjunction with the adjuvant Leukine (GM-CSF). The 27 patients enrolled in the study had previously received non-anti-CD20 cytoreductive therapy followed by ≥4 months of immune recovery prior to first vaccination. Of 11 patients who became evaluable at study conclusion, 82% (9/11) displayed a vaccine-induced, idiotype-specific cellular and/or humoral immune response. No patients showed serious adverse events (SAE) related to vaccination. The fully scalable plant-based manufacturing process yields safe and immunogenic personalized FL vaccines that can be produced within weeks of obtaining patient biopsies.
我们在一项I期安全性和免疫原性临床研究中报告了对用于靶向治疗B细胞滤泡性淋巴瘤(FL)的植物源性偶联疫苗的首次评估。每种重组个性化免疫原均由肿瘤衍生的、植物产生的独特型抗体(Ab)杂交体组成,该杂交体包含肿瘤相关轻链和重链Ab的高变区,并通过基因工程嫁接到常见的人IgG1支架上。每种免疫原均使用表达独特型Ab轻链和重链的双magnICON载体在本氏烟草植物中生产。每种纯化的Ab与载体蛋白钥孔血蓝蛋白(KLH)化学连接,形成偶联疫苗。通过一系列≥6次皮下注射并结合佐剂白细胞介素(GM-CSF)将疫苗接种给FL患者。参与该研究的27名患者此前接受了非抗CD20细胞减灭疗法,在首次接种疫苗前有≥4个月的免疫恢复时间。在研究结束时可进行评估的11名患者中,82%(9/11)表现出疫苗诱导的独特型特异性细胞和/或体液免疫反应。没有患者出现与接种疫苗相关的严重不良事件(SAE)。这种完全可扩展的基于植物的制造工艺可生产出安全且具有免疫原性的个性化FL疫苗,能够在获取患者活检样本后的数周内生产出来。