Møller Holger Jon, de Fost Maaike, Aerts Hans, Hollak Carla, Moestrup Søren Kragh
Department of Clinical Biochemistry, AKH Aarhus University Hospital, Aarhus, Denmark.
Eur J Haematol. 2004 Feb;72(2):135-9. doi: 10.1046/j.0902-4441.2003.00193.x.
Recently, soluble CD163 (sCD163) has been identified as a macrophage/monocyte-specific plasma protein and increased concentrations have been measured in patients with infection and myeloid leukaemia. In the present study we investigated the levels of sCD163 in patients with Gaucher's disease, an inherited lysosomal storage disorder characterised by hepato- and splenomegaly due to excessive accumulation of macrophages. The sCD163 plasma levels, median (25-75 percentiles), were far above the levels in normal subjects [7.1 mg/L (4.8-10.3) vs. 1.9 mg/L (1.5-2.4), P < 0.0001]. After initiation of enzyme supplementation therapy, the sCD163 levels were significantly reduced [4.7 mg/L (3.2-6.6), P = 0.0004]. sCD163 correlated with disease severity (rho = 0.43, P < 0.0061) and chitotriosidase activity (rho = 0.71, P > 0.0001). This study further establishes that sCD163 may be a valuable laboratory parameter in monitoring disease with increased macrophage activity.
最近,可溶性CD163(sCD163)已被确定为一种巨噬细胞/单核细胞特异性血浆蛋白,在感染患者和髓系白血病患者中检测到其浓度升高。在本研究中,我们调查了戈谢病患者的sCD163水平,戈谢病是一种遗传性溶酶体贮积症,其特征是由于巨噬细胞过度积累导致肝脾肿大。sCD163血浆水平,中位数(第25-75百分位数),远高于正常受试者的水平[7.1mg/L(4.8-10.3)对1.9mg/L(1.5-2.4),P<0.0001]。开始酶替代治疗后,sCD163水平显著降低[4.7mg/L(3.2-6.6),P=0.0004]。sCD163与疾病严重程度相关(rho=0.43,P<0.0061)和壳三糖苷酶活性相关(rho=0.71,P<0.0001)。这项研究进一步证实,sCD163可能是监测巨噬细胞活性增加的疾病的一个有价值的实验室参数。