Clinical Pathology, National Institute of Gastroenterology, S. de Bellis, Bari, Italy.
Immunopharmacol Immunotoxicol. 2008;30(4):687-700. doi: 10.1080/08923970802278177.
90K/Mac-2BP glycoprotein is involved in the immune defense against a variety of neoplasms and viral infections, modulating the activity of several effectors such as natural killer cells. Quite interestingly, 90K/Mac-2BP is associated to a poor response to interferon (IFN) alpha in hepatitis C virus (HCV) infected patients. Here, in 70 consecutive HCV chronic patients, we have evaluated 90K basal levels as a response predictor to combined therapy with Peginterferon and Ribavirin. We have found higher 90K levels in genotype 1/4 than in genotype 2/3 (p = 0.006) and in 62.5% of non-responders than in 20% of responders (p < 0.001). Genotype 1/4, higher 90K and gamma glutamyl transferase (gammaGT) levels resulted independently associated to a status of refractoriness to therapy. Consequently, evaluation of 90K serum levels seems to be a promising useful marker of response to combined therapy in HCV disease.
90K/Mac-2BP 糖蛋白参与针对多种肿瘤和病毒感染的免疫防御,调节自然杀伤细胞等多种效应物的活性。有趣的是,90K/Mac-2BP 与丙型肝炎病毒 (HCV) 感染患者对干扰素 (IFN)α反应不佳有关。在这里,我们在 70 例连续的 HCV 慢性患者中评估了 90K 的基础水平作为对聚乙二醇干扰素和利巴韦林联合治疗的反应预测因子。我们发现基因型 1/4 的 90K 水平高于基因型 2/3(p=0.006),无应答者的 90K 水平高于应答者的 20%(p<0.001)。基因型 1/4、较高的 90K 和谷氨酰转移酶 (gammaGT) 水平与对治疗的耐药性独立相关。因此,评估血清 90K 水平似乎是 HCV 疾病联合治疗反应的有前途的有用标志物。