Patel P M, Flemming C L, Russell S J, Eccles S A, Collins M K
Section of Cell and Molecular Biology, Institute of Cancer Research & Royal Marsden Hospital, London, U.K.
J Immunother Emphasis Tumor Immunol. 1993 Nov;14(4):310-3. doi: 10.1097/00002371-199311000-00010.
Cytokine gene therapy for cancer could involve either the direct delivery of cytokine genes to established tumours to stimulate their rejection or the injection of cytokine-secreting tumour cells to stimulate an immune response that could reduce metastatic disease. To assess the feasibility of the first approach, we have compared the ability of different cytokine-secreting tumour cells to induce the rejection of admixed, unmodified cells. While interleukin (IL)-2- or interleukin-4-secreting tumour cells were ineffective, interferon-gamma (IFN-gamma)-secreting cells could induce rejection of 10% admixed, unmodified cells. Because direct gene delivery to tumours is unlikely to be 100% efficient, these data suggest that IFN-gamma may be the most suitable of these cytokines for this approach. However, we have demonstrated that injection of IL-2-secreting tumour cells, following primary tumour excision, can prevent the development of metastases and prolong survival of rats. This suggests that IL-2-secreting tumour cells can be effective in the treatment of metastatic disease.
癌症的细胞因子基因治疗可能涉及将细胞因子基因直接导入已形成的肿瘤以刺激其被排斥,或者注射分泌细胞因子的肿瘤细胞以刺激免疫反应,从而减少转移性疾病。为了评估第一种方法的可行性,我们比较了不同分泌细胞因子的肿瘤细胞诱导混合的未修饰细胞被排斥的能力。虽然分泌白细胞介素(IL)-2或白细胞介素-4的肿瘤细胞无效,但分泌干扰素-γ(IFN-γ)的细胞可以诱导10%混合的未修饰细胞被排斥。由于将基因直接导入肿瘤不太可能达到100%的效率,这些数据表明IFN-γ可能是这些细胞因子中最适合这种方法的。然而,我们已经证明,在原发性肿瘤切除后注射分泌IL-2的肿瘤细胞,可以预防转移的发生并延长大鼠的生存期。这表明分泌IL-2的肿瘤细胞在治疗转移性疾病中可能有效。