Mildvan Donna, Spritzler John, Grossberg Sidney E, Fahey John L, Johnston David M, Schock Barbara R, Kagan Jonathan
Beth Israel Medical Center, New York, New York 10003, USA.
Clin Infect Dis. 2005 Mar 15;40(6):853-8. doi: 10.1086/427877. Epub 2005 Feb 18.
CD4+ T lymphocyte (CD4) counts and plasma human immunodeficiency virus (HIV) type 1 RNA concentrations predict clinical outcome in HIV-1 infection. Our objective was to assess the independent prognostic value for disease progression of soluble markers of immune system activation.
This retrospective marker-validation study utilized previously obtained clinical and laboratory data, including CD4+ cell counts, and made use of stored frozen serum samples to assay for levels of beta2-microglobulin, neopterin, endogenous interferon, triglycerides, interleukin-6, soluble tumor necrosis factor- alpha receptor II, and HIV-1 RNA, and to determine HIV genotypic reverse-transcriptase inhibitor resistance. The 152 patients who participated in this study represented a subsample of participants in AIDS Clinical Trials Group (ACTG) 116B/117, a randomized trial that demonstrated the clinical benefit of didanosine over zidovudine monotherapy in persons with advanced HIV-1 infection. Marker data were analyzed in relation to protocol-defined clinical disease progression, using Cox proportional hazards models.
The median duration of follow-up was 344 days. Elevated baseline values for neopterin (P=.0009), endogenous interferon (P=.00039) and interleukin-6 (P=.0007) were each associated with greater subsequent risk of clinical disease progression. In a head-to-head comparison that was adjusted for CD4+ cell count (P=.0165) and HIV-1 RNA level (P=.1220), we found that elevated values for neopterin (P=.0002) and, to a lesser extent, endogenous interferon (P=.0053) were the strongest predictors of increased risk of clinical disease progression 6 months later.
Soluble markers of immune activation add prognostic information to CD4 counts and viral load for risk of disease progression in advanced HIV-1 infection. The robust performance of neopterin, an inexpensive and reliably measured serum marker, supports its potential suitability for patient monitoring, particularly in resource-limited settings.
CD4 + T淋巴细胞(CD4)计数和血浆1型人类免疫缺陷病毒(HIV)RNA浓度可预测HIV - 1感染的临床结局。我们的目的是评估免疫系统激活的可溶性标志物对疾病进展的独立预后价值。
这项回顾性标志物验证研究利用了先前获得的临床和实验室数据,包括CD4 + 细胞计数,并使用储存的冷冻血清样本检测β2 - 微球蛋白、新蝶呤、内源性干扰素、甘油三酯、白细胞介素 - 6、可溶性肿瘤坏死因子 - α受体II和HIV - 1 RNA的水平,并确定HIV基因型逆转录酶抑制剂耐药性。参与本研究的152名患者代表了艾滋病临床试验组(ACTG)116B/117参与者的一个子样本,该随机试验证明了在晚期HIV - 1感染患者中,去羟肌苷比齐多夫定单药治疗具有临床益处。使用Cox比例风险模型分析标志物数据与方案定义的临床疾病进展的关系。
中位随访时间为344天。新蝶呤(P = 0.0009)、内源性干扰素(P = 0.00039)和白细胞介素 - 6(P = 0.0007)的基线值升高均与随后更大的临床疾病进展风险相关。在针对CD4 + 细胞计数(P = 0.0165)和HIV - 1 RNA水平(P = 0.1220)进行调整的直接比较中,我们发现新蝶呤值升高(P = 0.0002)以及在较小程度上内源性干扰素值升高(P = 0.0053)是6个月后临床疾病进展风险增加的最强预测因素。
免疫激活的可溶性标志物为晚期HIV - 1感染患者疾病进展风险的CD4计数和病毒载量增加了预后信息。新蝶呤作为一种廉价且测量可靠的血清标志物,其强大的性能支持了它在患者监测中的潜在适用性,特别是在资源有限的环境中。