H. Lee Moffitt Cancer Center & Research Institute, Immunology Department, SRB 23033, 12902 Magnolia Dr, Tampa, FL 33612, USA.
Expert Opin Emerg Drugs. 2012 Dec;17(4):519-41. doi: 10.1517/14728214.2012.736487. Epub 2012 Nov 20.
Myelodysplastic syndromes (MDS) are characterized by dysplastic morphologic features and ineffective hematopoiesis. Pathophysiological characteristics change over time making therapeutic development a major challenge. In early MDS, cytopenias arise or are exacerbated by humoral and cellular immune-mediators that suppress hematopoietic progenitor survival and alter the bone marrow microenvironment.
In this review, current immunosuppressive regimens are described. To identify new therapies that may enhance immunosuppressive therapy (IST) response and identify pharmacodynamic biomarkers for patient selection, the inflammasome, cytokines, metabolic pathways and signaling events are described.
Agents with the potential to induce early, durable hematologic remissions are needed and many new immunosuppressive agents are available for investigation. An immune-mediated mechanism is likely to contribute to MDS early after diagnosis. New approaches that interfere with inflammatory pathways in the bone marrow microenvironment may move closer toward sustained disease control in MDS.
骨髓增生异常综合征(MDS)的特征是存在病态造血特征和无效造血。随着时间的推移,病理生理特征发生变化,这使得治疗开发成为一个主要挑战。在早期 MDS 中,细胞减少症是由体液和细胞免疫介质引起的,这些介质会抑制造血祖细胞的存活并改变骨髓微环境。
在这篇综述中,描述了当前的免疫抑制方案。为了确定可能增强免疫抑制治疗(IST)反应的新疗法,并为患者选择确定药效动力学生物标志物,描述了炎症小体、细胞因子、代谢途径和信号事件。
需要有潜力诱导早期、持久血液学缓解的药物,并且有许多新的免疫抑制剂可供研究。免疫介导的机制可能有助于 MDS 在诊断后早期发生。干扰骨髓微环境中炎症途径的新方法可能更接近于 MDS 的持续疾病控制。