Mihich E
Grace Cancer Drug Center, Roswell Park Memorial Institute, New York State Department of Health, Buffalo 14263.
Cancer Detect Prev. 1988;12(1-6):531-5.
With increased knowledge of the mechanisms of host defenses against tumors, both immunological and nonimmunological in nature, and of the relationships between tumors and host cells, it becomes possible to develop agents aimed at modifying those relationships to therapeutic advantage. The task is facilitated by the advent of recombinant DNA technology, which makes it possible to produce biologicals in quantity and purity adequate for studies in vivo. The potentialities of biological response modifiers (BRMs) are primarily due to their specificity and/or selectivity of action, whether these attributes are related to receptors/antigens present on neoplastic cells or on cells of the immunological regulatory networks or to nonspecific activation of host defenses. The limitations are related to the fact that in certain cases treatments are too specific for a tumor cell within a heterogeneous cell population; these agents also show toxicities that, albeit usually unrelated to their antitumor action, can in some cases be severe.
随着对宿主抗瘤防御机制(包括免疫和非免疫性质的机制)以及肿瘤与宿主细胞之间关系的认识不断增加,开发旨在改变这些关系以获得治疗优势的药物成为可能。重组DNA技术的出现推动了这一任务的开展,该技术使得能够大量生产纯度足以用于体内研究的生物制品。生物反应调节剂(BRM)的潜力主要归因于其作用的特异性和/或选择性,无论这些特性是与肿瘤细胞或免疫调节网络细胞上存在的受体/抗原相关,还是与宿主防御的非特异性激活相关。其局限性在于,在某些情况下,治疗对异质性细胞群体中的肿瘤细胞过于特异;这些药物还表现出毒性,尽管通常与其抗肿瘤作用无关,但在某些情况下可能很严重。