Huang Wei, Tian Hou-wen, Ren Jiao, Fan Jiang-tao, Zhao Li, Bian Tao, Lu Zhen-hua, Ruan Li
Department of Gynecologic Oncology, The Affiliated Oncology Hospital, Guangxi Medical University, Nanning 530021, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2005 Sep;19(3):240-3.
To generate a human papillomavirus (HPV16) prophylactic and therapeutic vaccine candidate for cervical cancer.
HPV16 major capsid protein L1 gene/minor capsid protein L2 gene and HPV16 early E6/E7 genes were inserted into a vaccinia virus expression vector. A strain of non-recombinant vaccinia virus containing the sequences was obtained through a homologous recombination and identified.
DNA hybridization confirmed that the HPV16L1/L2/E6/E7 genes were integrated into vaccinia virus DNA. Western Blot result showed that full-length L1/L2/E6/E7 proteins were co-expressed in CEF cells infected with the recombinant virus.
NTVJE6E7CKL1L2 could be taken as a candidate of prophylactic and therapeutic vaccine for HPV-associated tumors and their precancerous transformations.
制备一种用于宫颈癌的人乳头瘤病毒(HPV16)预防性和治疗性候选疫苗。
将HPV16主要衣壳蛋白L1基因/次要衣壳蛋白L2基因以及HPV16早期E6/E7基因插入痘苗病毒表达载体。通过同源重组获得一株含有这些序列的非重组痘苗病毒并进行鉴定。
DNA杂交证实HPV16L1/L2/E6/E7基因已整合到痘苗病毒DNA中。蛋白质免疫印迹结果显示全长L1/L2/E6/E7蛋白在感染重组病毒的鸡胚成纤维细胞(CEF)中共同表达。
NTVJE6E7CKL1L2可作为HPV相关肿瘤及其癌前病变的预防性和治疗性疫苗候选物。