Carstens J, Teglbjaerg L S, Black F T
Department of Infectious Diseases, Marselisborg Hospital, University Hospital, Aarhus, Denmark.
Eur J Clin Chem Clin Biochem. 1995 Sep;33(9):559-62. doi: 10.1515/cclm.1995.33.9.559.
The purpose of this study was to evaluate the use of the biologic immune activation markers neopterin and beta 2-microglobulin in monitoring human immunodeficiency virus (HIV)-positive patients without acquired immunodeficiency syndrome (AIDS) treated with isoprinosine and placebo. Serum samples obtained at the commencement of study and samples obtained after 24 weeks were available from 277 HIV-positive patients in the Scandinavian multicentre isoprinosine trial. After 24 weeks' treatment, the concentrations of beta 2-microglobulin and neopterin had increased both in the isoprinosine group and the placebo group. However, in the isoprinosine group the relative increase within beta 2-microglobulin was significantly smaller. Within neopterin, the increase from baseline level was small and not significantly different from the change in the placebo group. The beta 2-microglobulin data might reflect a suppressive effect of isoprinosine on the HIV-induced activation of the cellular immune system. Because of the minor changes, there is no real evidence of neopterin and beta 2-microglobulin being valuable as surrogate markers in monitoring therapy effects of isoprinosine.
本研究的目的是评估生物免疫激活标志物新蝶呤和β2-微球蛋白在监测接受异丙肌苷和安慰剂治疗的未患获得性免疫缺陷综合征(AIDS)的人类免疫缺陷病毒(HIV)阳性患者中的应用。在斯堪的纳维亚多中心异丙肌苷试验中,可获得277例HIV阳性患者在研究开始时采集的血清样本以及24周后采集的样本。经过24周的治疗,异丙肌苷组和安慰剂组的β2-微球蛋白和新蝶呤浓度均有所升高。然而,在异丙肌苷组中,β2-微球蛋白的相对升高明显较小。在新蝶呤方面,从基线水平的升高较小,与安慰剂组的变化无显著差异。β2-微球蛋白数据可能反映了异丙肌苷对HIV诱导的细胞免疫系统激活的抑制作用。由于变化较小,没有实际证据表明新蝶呤和β2-微球蛋白可作为监测异丙肌苷治疗效果的替代标志物。