Department of Experimental Virology, Institutute of Hematology & Blood Transfusion, Prague, Czech Republic.
Immunotherapy. 2010 Mar;2(2):227-41. doi: 10.2217/imt.10.2.
In spite of the considerable successes that have been achieved in the treatment of chronic myeloid leukemia (CML), cure for the disease can only be obtained by the present means in a rather small minority of patients. During the past decade, considerable progress has been made in the understanding of the immunology of CML, which has raised hopes that this disease may be curable by supplementing the current targeted chemotherapy with immunotherapeutic approaches. More than ten small-scale clinical trials have been carried out with experimental vaccines predominantly based on the p210bcr-abl fusion protein. Their results suggested beneficial effects in some patients. Recent data obtained in human patients as well as in animal models indicate that the p210bcr-abl protein does not carry the immunodominant epitope(s). These observations, combined with the recognition of an ever increasing number of other immunogenic proteins in CML cells, strongly support the concept that gene-modified, cell-based vaccines containing the full spectrum of tumor antigens might be the most effective immunotherapeutic approach. Recently created mathematical models have provided important leads for the timing of the combination of targeted drug therapy with vaccine administration. A strategy of how targeted drug therapy might be combined with vaccination is outlined.
尽管在治疗慢性髓细胞白血病 (CML) 方面取得了相当大的成功,但目前只有少数患者能够通过现有手段治愈该疾病。在过去的十年中,人们对 CML 的免疫学有了更深入的了解,这增加了人们的希望,即通过补充目前的靶向化疗与免疫治疗方法,可能治愈这种疾病。已经进行了十多项基于 p210bcr-abl 融合蛋白的实验性疫苗的小型临床试验。其结果表明对一些患者有有益的影响。最近在人类患者和动物模型中获得的数据表明,p210bcr-abl 蛋白不携带免疫优势表位。这些观察结果,加上对 CML 细胞中越来越多其他免疫原性蛋白的认识,强烈支持这样一种概念,即包含肿瘤抗原全谱的基因修饰、基于细胞的疫苗可能是最有效的免疫治疗方法。最近创建的数学模型为靶向药物治疗与疫苗接种联合的时机提供了重要线索。概述了靶向药物治疗与疫苗接种联合的策略。