Janson R W, Arend W P
Bull Rheum Dis. 1992;41(3):6-8.
Modern techniques of genetic engineering have led to the development of novel receptor-targeted immunotherapies for human diseases. These new approaches include mAbs to the CD4+ subset of T cells, immunotoxins for CD5+ T cells, a diphtheria toxin coupled to IL-2, and antibodies to specific TCRs. Additional approaches include a specific IL-1 receptor antagonist and soluble receptors for IL-1 or TNF. Although initially promising, these new approaches to altering immune and inflammatory events need to be thoroughly and carefully evaluated in further clinical trials in human diseases. Perhaps these novel forms of receptor-targeted immunotherapy will eventually prove to be most effective when employed in combination with more conventional anti-inflammatory and immunosuppressive medications.
现代基因工程技术已促成针对人类疾病的新型受体靶向免疫疗法的发展。这些新方法包括针对T细胞CD4 +亚群的单克隆抗体、针对CD5 + T细胞的免疫毒素、与白细胞介素-2偶联的白喉毒素,以及针对特定T细胞受体的抗体。其他方法包括特异性白细胞介素-1受体拮抗剂和白细胞介素-1或肿瘤坏死因子的可溶性受体。尽管这些改变免疫和炎症反应的新方法最初很有前景,但需要在人类疾病的进一步临床试验中进行全面且仔细的评估。也许这些新型受体靶向免疫疗法最终与更传统的抗炎和免疫抑制药物联合使用时会被证明是最有效的。