Qian Xinlai, Lu Yuanzhi, Liu Qiao, Chen Ke, Zhao Qingzheng, Song Jietao
Department of Cellular and Molecular Biology, Cancer Institute & Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, PR China.
Immunol Lett. 2006 Feb 15;102(2):191-201. doi: 10.1016/j.imlet.2005.09.004. Epub 2005 Oct 5.
Human papillomaviruses (HPVs), particularly HPV-16, are not only causally linked to cervical cancers but also play an important role in the development of other cancers. The oncoproteins, E6 and E7, are consistently coexpressed in the majority of HPV-containing carcinomas and their metastatic lesions, and are critical to the induction and maintenance of malignant phenotype, and also can cause tumor metastasis. Therefore, E6 and E7 represent ideal tumor-specific antigens for the development of immunotherapy to prevent and treat HPV-associated cancers and their metastases. The powerful antigenic nature of Mycobacterium tuberculosis heat shock protein 70 (TBhsp70) is emphasized by evidence that mammals are capable of recognizing murine and human multiple B and T cell epitopes in this protein, and therefore allows it to be used as an adjuvant-free carrier to stimulate the immune response to a covalently linked fusion partner. In our present study, we developed a recombinant TBhsp70Delta protein expression vector that permits the production of other protein fused to TBhsp70Delta. A recombinant HPV-16mE6Delta/mE7/TBhsp70Delta fusion protein was expressed and purified, and immunization with the fusion protein in the absence of adjuvant was capable of providing strong protection to C57BL/6 mice against challenge and rechallenge with TC-1 cells, but not HPV negative Lewis lung cancer cells, and induced established TC-1 tumor regression and led to long-term survival. Consistent with the in vivo results, the fusion protein immunization in the absence of adjuvant induced cytolytic T lymphocytes recognized specifically TC-1 tumor cells in vitro. We also demonstrated that immunization with the fusion protein in the absence of adjuvant was effective in both preventing and treating TC-1 metastatic lesions in the lung metastasis model. In particular, immunization with the fusion protein caused regression of established lung metastatic lesions in 50% of immunized animals. This study represents an instance of tumor therapy with a TBhsp70Delta fusion protein and provides the scientific basis for the clinical application of the HPV16mE6Delta/mE7/TBhsp70Delta fusion protein in the treatment of HPV-associated cancers and their metastases.
人乳头瘤病毒(HPV),尤其是HPV - 16,不仅与宫颈癌存在因果关联,在其他癌症的发生发展中也起着重要作用。癌蛋白E6和E7在大多数含HPV的癌组织及其转移病灶中持续共表达,对恶性表型的诱导和维持至关重要,还可导致肿瘤转移。因此,E6和E7是开发免疫疗法以预防和治疗HPV相关癌症及其转移的理想肿瘤特异性抗原。结核分枝杆菌热休克蛋白70(TBhsp70)强大的抗原性体现在以下证据中:哺乳动物能够识别该蛋白中的鼠源和人源多个B细胞和T细胞表位,因此可将其用作无佐剂载体来刺激针对共价连接的融合伙伴的免疫反应。在我们目前的研究中,我们构建了一种重组TBhsp70Delta蛋白表达载体,可用于生产与TBhsp70Delta融合的其他蛋白。表达并纯化了重组HPV - 16mE6Delta/mE7/TBhsp70Delta融合蛋白,在无佐剂情况下用该融合蛋白免疫能够为C57BL / 6小鼠提供强大保护,使其免受TC - 1细胞的攻击和再次攻击,但对HPV阴性的Lewis肺癌细胞无效,还能诱导已形成的TC - 1肿瘤消退并实现长期存活。与体内结果一致,在无佐剂情况下用融合蛋白免疫可在体外诱导细胞毒性T淋巴细胞特异性识别TC - 1肿瘤细胞。我们还证明,在无佐剂情况下用融合蛋白免疫在肺转移模型中对预防和治疗TC - 1转移病灶均有效。特别是,用融合蛋白免疫可使50%的免疫动物体内已形成的肺转移病灶消退。本研究展示了用TBhsp70Delta融合蛋白进行肿瘤治疗的实例,并为HPV16mE6Delta/mE7/TBhsp70Delta融合蛋白在治疗HPV相关癌症及其转移方面的临床应用提供了科学依据。