Laboratory of Clinical Epidemiology and Center for the Study of Myelofibrosis, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.
Leuk Res. 2011 May;35(5):563-5. doi: 10.1016/j.leukres.2011.01.013. Epub 2011 Feb 5.
The dominant pathophysiological and clinical features of myeloproliferative neoplasm (MPN)-associated myelofibrosis are caused by bone marrow fibrosis. It is widely believed this fibrosis is a reaction to the MPN-clone implying the cells causing fibrosis are polyclonal and genetically unrelated to the MPN-clone. We cite recent data illustrating the complexity of cell types comprising the bone marrow micro-environment and showing that at least some of the cells responsible for bone marrow fibrosis are clonal and genetically related to the MPN-clone.
骨髓纤维化是骨髓增生性肿瘤(MPN)相关的骨髓纤维化的主要病理生理和临床特征,它被广泛认为是对 MPN 克隆的反应,这意味着导致纤维化的细胞是多克隆的,与 MPN 克隆在遗传上无关。我们引用了最近的数据来说明构成骨髓微环境的细胞类型的复杂性,并表明至少有一些导致骨髓纤维化的细胞是克隆的,与 MPN 克隆在遗传上有关。