Saji S, Sugiyama Y, Kunieda K, Umemoto T
Second Dept. of Surgery, Gifu University School of Medicine.
Gan To Kagaku Ryoho. 1999 Jun;26 Suppl 1:32-41.
After approval of national health insurance for non-specific immunomodulation such as OK-432 (1978) and PSK (1980), lentinan, SPG, bestatin and dried BCG vaccine have been tried. Including cytokines such as IL-2, IL-12, IFN, TNF or monoclonal antibodies, they have been widely used as biological response modifiers (BRM). Progress in BRM therapy may be broken down into the first 10 years as development, the next 10 years as disappointment and the most recent 5 years as dream-like progress owing to molecular biological techniques. An interdisciplinary approach has been taken by the Japanese Research Society for Surgical Cancer Immunology, founded in 1980, and the Japanese Society of BRM founded in 1988. Many investigations have been performed on issues such as the clinical evaluation or criteria for responder cases, host immunocompetency, post-operative adjuvant immuno-chemotherapy, locoregional immunotherapy, cytokine therapy, adoptive immunotherapy, and tumor specific immunotherapy. Attention has also focused on malignant tumor injury, surgical stress, the advantages or disadvantages of splenectomy, and discussions of the current status and future prospects in the next century for new BRM therapy.
在国家医疗保险批准使用诸如OK-432(1978年)和PSK(1980年)等非特异性免疫调节剂之后,香菇多糖、裂褶菌多糖、贝司他汀和冻干卡介苗也进行了试用。包括白细胞介素-2、白细胞介素-12、干扰素、肿瘤坏死因子等细胞因子或单克隆抗体在内,它们已被广泛用作生物反应调节剂(BRM)。由于分子生物学技术,BRM疗法的进展可分为最初10年的发展期、接下来10年的失望期以及最近5年如梦似幻的进展期。1980年成立的日本外科癌症免疫学会和1988年成立的日本BRM学会都采取了跨学科的方法。针对诸如临床评估或反应者病例标准、宿主免疫能力、术后辅助免疫化疗、局部区域免疫治疗、细胞因子治疗、过继性免疫治疗以及肿瘤特异性免疫治疗等问题,已经开展了许多研究。关注点还集中在恶性肿瘤损伤、手术应激、脾切除术的利弊,以及对下个世纪新BRM疗法的现状和未来前景的讨论上。