Krown S E
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
J Interferon Cytokine Res. 1998 Apr;18(4):209-14. doi: 10.1089/jir.1998.18.209.
This article reviews developments over nearly 15 years in the application of interferon-alpha (IFN-alpha) to the treatment of Kaposi's sarcoma (KS) in patients with acquired immunodeficiency syndrome (AIDS). The initial success of IFN treatment for selected patients with AIDS-associated KS occurred before identification of the human immunodeficiency virus (HIV) and in the absence of any coherent view of KS pathogenesis. A more comprehensive understanding of the biology of both AIDS and KS, together with increased knowledge of the biologic effects of IFN and therapeutic advances in the treatment of HIV infection, have made IFN therapy for KS both more rational and more successful. There is every reason to believe that the current results with IFN for KS can be improved on by capitalizing on recent improvements in HIV therapy and the availability of specific inhibitors of angiogenic cytokines. I sincerely thank the Milstein family and my colleagues in the International Society for Interferon and Cytokine Research (ISICR) for recognizing this work, which is the product of many collaborations between clinical and basic scientists in my own institution and elsewhere.
本文回顾了近15年来α干扰素(IFN-α)在治疗获得性免疫缺陷综合征(AIDS)患者的卡波西肉瘤(KS)方面的进展。IFN治疗某些艾滋病相关KS患者的初步成功发生在人类免疫缺陷病毒(HIV)被发现之前,而且当时对KS发病机制尚无任何连贯的认识。对AIDS和KS生物学的更全面理解,以及对IFN生物学效应的更多了解和HIV感染治疗方面的进展,使得IFN治疗KS更加合理且更成功。完全有理由相信,通过利用HIV治疗的最新进展以及血管生成细胞因子特异性抑制剂的可得性,目前IFN治疗KS的结果可以得到改善。我衷心感谢米尔斯坦家族以及国际干扰素和细胞因子研究协会(ISICR)的同事们认可这项工作,它是我所在机构和其他地方的临床和基础科学家之间多次合作的成果。