Division of Medical Genetics, School of Medicine, University of Washington, Seattle, WA, USA.
PAI Life Sciences, Seattle, WA, USA.
Sci Rep. 2022 May 11;12(1):7753. doi: 10.1038/s41598-022-11843-z.
Our goal is to overcome treatment resistance in ovarian cancer patients which occurs in most cases after an initial positive response to chemotherapy. A central resistance mechanism is the maintenance of desmoglein-2 (DSG2) positive tight junctions between malignant cells that prevents drug penetration into the tumor. We have generated JO4, a recombinant protein that binds to DSG2 resulting in the transient opening of junctions in epithelial tumors. Here we present studies toward the clinical translation of c-JO4 in combination with PEGylated liposomal doxorubicin/Doxil for ovarian cancer therapy. A manufacturing process for cGMP compliant production of JO4 was developed resulting in c-JO4. GLP toxicology studies using material from this process in DSG2 transgenic mice and cynomolgus macaques showed no treatment-related toxicities after intravenous injection at doses reaching 24 mg/kg. Multiple cycles of intravenous c-JO4 plus Doxil (four cycles, 4 weeks apart, simulating the treatment regimen in the clinical trial) elicited antibodies against c-JO4 that increased with each cycle and were accompanied by elevation of pro-inflammatory cytokines IL-6 and TNFα. Pretreatment with steroids and cyclophosphamide reduced anti-c-JO4 antibody response and blunted cytokine release. Our data indicate acceptable safety of our new treatment approach if immune reactions are monitored and counteracted with appropriate immune suppression.
我们的目标是克服卵巢癌患者的治疗耐药性,这种耐药性在大多数情况下发生在初始化疗反应阳性后。一个主要的耐药机制是维持恶性细胞之间的桥粒芯糖蛋白 2(DSG2)阳性紧密连接,阻止药物渗透到肿瘤中。我们已经生成了 JO4,这是一种与 DSG2 结合的重组蛋白,导致上皮肿瘤中连接的短暂开放。在这里,我们提出了将 c-JO4 与聚乙二醇化脂质体阿霉素/多柔比星联合用于卵巢癌治疗的临床转化研究。开发了符合 cGMP 标准的 JO4 生产工艺,得到了 c-JO4。使用该工艺的材料在 DSG2 转基因小鼠和食蟹猴中进行的 GLP 毒理学研究表明,在 24mg/kg 的剂量下静脉注射后没有与治疗相关的毒性。多次静脉注射 c-JO4 加多柔比星(每 4 周 4 个周期,模拟临床试验中的治疗方案)会引发针对 c-JO4 的抗体,每个周期都会增加,同时伴随着促炎细胞因子 IL-6 和 TNFα 的升高。预先用类固醇和环磷酰胺治疗可降低抗 c-JO4 抗体反应并减轻细胞因子释放。如果免疫反应得到监测并通过适当的免疫抑制来对抗,我们的数据表明我们的新治疗方法具有可接受的安全性。