Dufour Carlo, Corcione Anna, Svahn Johanna, Haupt Riccardo, Poggi Vincenzo, Béka'ssy Albert Nandor, Scimè Rosanna, Pistorio Angela, Pistoia Vito
Hematology Unit, Department of Pediatric Hematology-Oncology, G. Gaslini Children's Hospital, Largo G Gaslini 5, 16147 Genoa, Italy.
Blood. 2003 Sep 15;102(6):2053-9. doi: 10.1182/blood-2003-01-0114. Epub 2003 May 15.
In Fanconi anemia (FA) C mice tumor necrosis factor alpha (TNF-alpha) and interferon gamma (IFN-gamma) have key roles in the pathogenesis of bone marrow failure. In FA subjects TNF-alpha was found to be increased in the serum and overproduced by patient-derived B-cell lines. In acquired aplastic anemia, a disease in which, similarly to FA, marrow failure occurs, TNF-alpha and IFN-gamma act as late mediators of the stem cell damage and are overexpressed in patient marrow lymphocytes. This study evaluated in marrow mononuclear cells (MNCs) of patients with FA, the expression of negative modulators of the hematopoiesis, such as TNF-alpha, IFN-gamma, macrophage inflammatory protein 1alpha (MIP-1alpha), and surface Fas ligand, and the role of TNF-alpha on FA erythropoiesis in vitro. TNF-alpha and IFN-gamma were significantly overexpressed in stimulated marrow MNCs of FA patients as compared to healthy controls. MIP-1alpha and Fas ligand were undetectable in patients and controls. In bone marrow cultures, the addition of anti-TNF-alpha increased the size and significantly increased the number of erythroid colony-forming units and erythroid burst-forming units grown from FA patients but not from healthy controls. This indicates that FA subjects have a marrow TNF-alpha activity that inhibits erythropoiesis in vitro. TNF-alpha has a relevant role in the pathogenesis of erythroid failure in FA patients.
在范可尼贫血(FA)C小鼠中,肿瘤坏死因子α(TNF-α)和干扰素γ(IFN-γ)在骨髓衰竭的发病机制中起关键作用。在FA患者中,发现血清中TNF-α升高,且患者来源的B细胞系产生过多。在获得性再生障碍性贫血(一种与FA类似会发生骨髓衰竭的疾病)中,TNF-α和IFN-γ作为干细胞损伤的晚期介质,在患者骨髓淋巴细胞中过度表达。本研究评估了FA患者骨髓单个核细胞(MNCs)中造血负调节因子的表达,如TNF-α、IFN-γ、巨噬细胞炎性蛋白1α(MIP-1α)和表面Fas配体,以及TNF-α在体外对FA红细胞生成的作用。与健康对照相比,FA患者受刺激的骨髓MNCs中TNF-α和IFN-γ显著过度表达。患者和对照中均未检测到MIP-1α和Fas配体。在骨髓培养中,添加抗TNF-α可增加FA患者而非健康对照所培养的红系集落形成单位和红系爆式集落形成单位的大小并显著增加其数量。这表明FA患者的骨髓具有TNF-α活性,可在体外抑制红细胞生成。TNF-α在FA患者红系衰竭的发病机制中起重要作用。