Ravandi Farhad, O'Brien Susan
Department of Leukemia, University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd., Box 428, Houston, TX 77030-4095, USA.
Cancer Immunol Immunother. 2006 Feb;55(2):197-209. doi: 10.1007/s00262-005-0015-8. Epub 2005 Jul 16.
Over the past decade, the introduction of nucleoside analogs and monoclonal antibodies into the treatment of patients with chronic lymphocytic leukemia (CLL) has resulted in higher rates and longer duration of response. This is a significant step towards achieving the ultimate goal of disease-eradication and improved survival. A continuing problem, however, is the susceptibility of these patients to infections. Profound dysregulation of the host immune system in patients with CLL and its impact on the clinical course of the disease are well established. A number of investigators have sought to identify the mechanisms underlying this innate immune dysfunction, which is further exacerbated by the actions of the potent therapeutic agents. The early recognition of infections as well as prophylactic administration of appropriate antibiotics has been the mainstay of managing infections in patients with CLL. Hopefully, increasing understanding of the molecular events underlying the neoplastic change in CLL will lead to more targeted and less immunosuppressive therapeutic modalities. Furthermore, the understanding of the mechanisms of immune dysfunction in CLL is of pivotal importance in the novel immune-based therapeutic strategies currently under development.
在过去十年中,将核苷类似物和单克隆抗体引入慢性淋巴细胞白血病(CLL)患者的治疗,已使缓解率提高且缓解持续时间延长。这是朝着实现根除疾病和提高生存率这一最终目标迈出的重要一步。然而,一个持续存在的问题是这些患者易受感染。CLL患者体内宿主免疫系统的严重失调及其对疾病临床进程的影响已得到充分证实。许多研究人员试图确定这种先天性免疫功能障碍的潜在机制,而强效治疗药物的作用会进一步加剧这种功能障碍。早期识别感染以及预防性使用适当的抗生素一直是CLL患者感染管理的主要手段。有望对CLL肿瘤性变化背后分子事件的深入理解,将带来更具针对性且免疫抑制性更低的治疗方式。此外,了解CLL免疫功能障碍的机制对于目前正在研发的基于免疫的新型治疗策略至关重要。