Genome Sciences Centre, British Columbia Cancer Research Centre, 675 West 10th Avenue, Vancouver, BC, Canada.
Hematol Oncol Clin North Am. 2010 Apr;24(2):343-59. doi: 10.1016/j.hoc.2010.02.008.
Myelodysplastic syndromes (MDS) are heterogeneous clonal hematologic malignancies characterized by cytopenias caused by ineffective hematopoiesis and propensity to progress to acute myeloid leukemia. Innate immunity provides immediate protection against pathogens by coordinating activation of signaling pathways in immune cells. Given the prominent role of the innate immune pathway in regulating hematopoiesis, it is not surprising that aberrant signaling of this pathway is associated with hematologic malignancies. Increased activation of the innate immune pathway may contribute to dysregulated hematopoiesis, dysplasia, and clonal expansion in myelodysplastic syndromes.
骨髓增生异常综合征(MDS)是一种异质性克隆性血液系统恶性肿瘤,其特征为无效造血导致的血细胞减少,并倾向于发展为急性髓系白血病。先天免疫系统通过协调免疫细胞中信号通路的激活,为机体提供针对病原体的即时保护。鉴于先天免疫通路在调节造血中的突出作用,该通路的异常信号与血液系统恶性肿瘤相关也就不足为奇了。先天免疫通路的过度激活可能导致骨髓增生异常综合征中造血功能紊乱、发育异常和克隆性扩张。