Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, China.
J Cell Mol Med. 2010 Jun;14(6B):1836-44. doi: 10.1111/j.1582-4934.2009.00818.x. Epub 2009 Jul 20.
In situ gene therapy with granulocyte-macrophage colony-stimulating factor (GM-CSF) was demonstrated to successfully inhibit tumour cell growth in a mouse orthotopic bladder cancer model, but suffered from several disadvantages, such as limited efficiency for gene delivery, low expression efficiency of the transgene and the safety concern resulting from viral vector. In order to address the limits, a novel immunotherapy was developed attentively through immobilization of streptavidin-tagged bioactive GM-CSF on the biotinylated mucosal surface of bladder wall on the basis of both the unique property of streptavidin (SA) to bind rapidly and almost irreversibly to any biotin-linked molecule and the outstanding ability of biotin to be incorporated easily into the proteins on the cell surface. The mouse orthotopic model of MB49 bladder cancer was used to evaluate the feasibility and efficacy of the novel immunotherapy performed twice a week for 3 weeks. Briefly, 1 day after intravesical implantation of 1 x 10(6) MB49 tumour cells in C57BL/6 mouse, 100 microl of 1 mg/ml NHS-PEO4-biotin was instilled and allowed to incubate in the bladder for 30 min., followed by intravesical instillation of 100 microl of 0.15 mg/ml SA-GM-CSF bifunctional fusion protein and incubation for 1 hr. SA-GM-CSF fusion protein was shown to be immobilized efficiently and durably on the biotinylated mucosal surface of bladder wall. The bladder cancer incidence was dramatically decreased from 100% in the control group to 37.5% in the SA-GM-CSF group. Importantly, 70% of the SA-GM-CSF-cured mice were protected against a second intravesical wild-type MB49 tumour challenge, indicating that an effective anti-tumour immunity was generated against MB49 bladder cancer. Thus, the novel immunotherapy may be an attractive therapeutic alternative and should be evaluated in bladder cancer patients.
粒细胞-巨噬细胞集落刺激因子(GM-CSF)的原位基因治疗已被证明可成功抑制小鼠原位膀胱癌模型中的肿瘤细胞生长,但存在一些缺点,例如基因传递效率有限、转基因表达效率低以及病毒载体带来的安全性问题。为了解决这些限制,我们通过将生物素化的 GM-CSF 固定在膀胱壁的生物素化黏膜表面上,开发了一种新型免疫疗法,该方法基于链霉亲和素(SA)与任何生物素化分子快速且几乎不可逆结合的独特特性,以及生物素很容易掺入细胞表面蛋白的出色能力。使用 MB49 膀胱癌的小鼠原位模型来评估该新型免疫疗法的可行性和疗效,该疗法每周进行两次,持续 3 周。简要地说,在 C57BL/6 小鼠中经膀胱内植入 1x10(6)MB49 肿瘤细胞 1 天后,将 100µl 的 1mg/ml NHS-PEO4-生物素注入膀胱并孵育 30min,随后经膀胱内注入 100µl 的 0.15mg/ml SA-GM-CSF 双功能融合蛋白并孵育 1 小时。SA-GM-CSF 融合蛋白被证明可有效地、持久地固定在膀胱壁的生物素化黏膜表面上。与对照组的 100%膀胱癌发生率相比,SA-GM-CSF 组的膀胱癌发生率显著降低至 37.5%。重要的是,70%接受 SA-GM-CSF 治疗的小鼠可免受第二次经膀胱内野生型 MB49 肿瘤挑战的影响,表明针对 MB49 膀胱癌产生了有效的抗肿瘤免疫。因此,这种新型免疫疗法可能是一种有吸引力的治疗选择,应该在膀胱癌患者中进行评估。