The Roberts-Guthman Chair in Immunopharmacology, Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, P.O. Box 39040, Tel Aviv, 69978, Israel,
Cancer Immunol Immunother. 2014 Jan;63(1):1-9. doi: 10.1007/s00262-013-1462-2. Epub 2013 Aug 17.
Cancer, the most devastating chronic disease affecting humankind, is treated primarily by surgery, chemotherapy, and radiation therapy. Surgery and radiotherapy are mainly used for debulking the primary tumor, while chemotherapy is the most efficient anti-metastatic treatment. To control better metastatic cancer, the host immune system should be stimulated. Yet, successful specific stimulation of the immune system against tumors was seldom achieved even in antigenic tumors. Our working hypothesis is that aggressive in situ tumor ablation can release tumor antigens and danger signals, which will enhance anti-tumor T cell responses resulting in the destruction of residual malignant cells in primary tumors and distant metastases. We developed two efficient in situ ablation treatments for solid cancer, which can be used to destroy the primary tumors and stimulate anti-tumor immune responses. The first treatment, electrochemical ablation, is applied through intratumoral electrodes, which deliver unipolar-pulsed electric currents. The second treatment, diffusing alpha-emitters radiation therapy (DaRT), is based on intratumoral (224)Ra-loaded wire(s) that release by recoil its daughter atoms. These short-lived alpha-emitting atoms spread in the tumor and spray it with lethal alpha particles. It was confirmed that these treatments effectively destroy various malignant animal and human primary solid tumors. As a consequence of such tumor ablation, tumor-derived antigenic material was released and provoked systemic T cell-dependent anti-tumor immunological reactions. These reactions conferred protection against a secondary tumor challenge and destroyed remaining malignant cells in the primary tumor as well as in distant metastases. Such anti-tumor immune responses could be further amplified by the immune adjuvant, CpG. Electrochemical ablation or DaRT together with chemotherapy and immunostimulatory agents can serve as treatment protocols for solid metastatic tumors and can be applied instead of or in combination with surgery.
癌症是影响人类的最具破坏性的慢性疾病,主要通过手术、化疗和放射治疗来治疗。手术和放射治疗主要用于清除原发性肿瘤,而化疗是最有效的抗转移治疗方法。为了更好地控制转移性癌症,应该刺激宿主的免疫系统。然而,即使在抗原性肿瘤中,成功地特异性刺激免疫系统对抗肿瘤也很少实现。我们的工作假设是,积极的原位肿瘤消融可以释放肿瘤抗原和危险信号,这将增强抗肿瘤 T 细胞反应,导致原发性肿瘤和远处转移的残留恶性细胞的破坏。我们开发了两种有效的原位消融治疗实体瘤的方法,可用于破坏原发性肿瘤并刺激抗肿瘤免疫反应。第一种治疗方法是电化学消融,通过肿瘤内电极应用,电极输送单极脉冲电流。第二种治疗方法是扩散α发射体辐射治疗(DaRT),基于肿瘤内(224)Ra 装载的电线,其通过反冲释放其子原子。这些短寿命的α发射原子在肿瘤中扩散,并喷洒致命的α粒子。已经证实,这些治疗方法有效地破坏了各种恶性动物和人类原发性实体肿瘤。由于这种肿瘤消融,肿瘤来源的抗原物质被释放,并引发全身性 T 细胞依赖性抗肿瘤免疫反应。这些反应赋予了对二次肿瘤挑战的保护,并破坏了原发性肿瘤和远处转移中的残留恶性细胞。这种抗肿瘤免疫反应可以通过免疫佐剂 CpG 进一步放大。电化学消融或 DaRT 联合化疗和免疫刺激剂可作为实体转移性肿瘤的治疗方案,可替代或与手术联合应用。