Malignant Hematology Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Cancer Control. 2013 Jan;20(1):49-59. doi: 10.1177/107327481302000108.
In the current treatment paradigms for leukemias, hematopoietic stem cell transplant (HSCT) is considered the best option with a curative potential although more often than not it simply delays disease progression. Advances are needed, both in current therapies and in the development of new strategies. Partly from studying the nuances of the curative potential of stem cell transplant, we have come to appreciate the relevance of the immune response and the potential of immunotherapy.
This review article summarizes the recent advances in the field of immunology and immunotherapy for leukemia.
In passive immunotherapy, recent progress in chimeric T-cell antigen receptor technology has been encouraging. In active immunotherapy, a cancer vaccine may potentially enhance HSCT. An overview of various clinical studies of peptide vaccination strategies focusing on molecular targets such as the Wilms' tumor gene 1 (WT1), proteinase 3 (PR3), and receptor for hyaluronan acid-mediated motility (RHAMM) is provided. Cell-based vaccination strategies are also briefly explored.
The immune system clearly has the capacity to recognize and react to leukemic cells, and recent evidence directs our attention to the importance of mounting inflammatory and CD4 T-cell responses to complement and support the cytotoxic activity elicited by peptide vaccines.
在当前的白血病治疗模式中,造血干细胞移植(HSCT)被认为是最有治愈潜力的选择,尽管它往往只是延迟了疾病的进展。需要在现有疗法和新策略的开发方面取得进展。部分原因是我们从研究干细胞移植的治愈潜力的细微差别中,开始认识到免疫反应的相关性和免疫疗法的潜力。
本文综述了白血病免疫和免疫治疗领域的最新进展。
在被动免疫治疗中,嵌合 T 细胞抗原受体技术的最新进展令人鼓舞。在主动免疫治疗中,癌症疫苗可能增强 HSCT。本文概述了各种针对分子靶点(如 Wilms 瘤基因 1(WT1)、蛋白酶 3(PR3)和透明质酸介导的运动受体(RHAMM))的肽疫苗策略的临床研究。还简要探讨了基于细胞的疫苗接种策略。
免疫系统显然有能力识别和反应白血病细胞,最近的证据使我们注意到产生炎症和 CD4 T 细胞反应以补充和支持肽疫苗引起的细胞毒性活性的重要性。