Novel strategies to augment genetically delivered immunotoxin molecular therapy for cancer therapy

作者：Liu, X; Wu, J; Zhang, S; Li, C; Huang, Q^*

来源：Cancer Gene Therapy, 2009, 16(11): 861-872.

DOI：10.1038/cgt.2009.30

• adenovirus
• conditionally replicative adenovirus (CRAd)
• replicative deficient adenovirus
• immunotoxin
• tumor

Immunotoxin therapy is a promising molecular cancer treatment strategy. Its main advantage is seletive cytotoxicity towards tumor cells and minimal toxicity in normal tissues. However, a short half-life and rapid clearance severely hampers its clinical application. We report here a novel genetic approach in which a recombinant adenovirus vector was used to deliver an immunotoxin gene e23(scFv)-PE40 targeted to the oncogene c-erbB-2 (also known as Her2/neu). This vector, when combined with a low dose of a conditionally replicative adenovirus vector (CRAd), has enhanced tumor-killing ability either alone or in combination with the chemotherapeutic agent etoposide. Our data show that low-dose CRAd facilitated the replication of replication-deficient Ade-23(scFv)-PE40 up to 6-20 times and the transcription of e23(scFv)-PE40 gene up to 12 times. Moreover, etoposide increased the e23(scFv)-PE40 transcription up to 8.5 times. Furthermore, we show that systemic application of Ad-e23(scFv)-PE40 and enhanced expression of the immunotoxin gene was well tolerated as determined by serum biochemical markers and histological examination of most vital organs. Taken together, our data support a novel genetic immunotoxin delivery approach that may yield enhanced efficacy against a variety of Her2/neu-expressing tumors. Cancer Gene Therapy (2009) 16, 861-872; doi: 10.1038/cgt.2009.30; published online 22 May 2009

• 出版日期2009-11
• 单位上海交通大学