Department of Biochemistry, Genetics and Immunology, Faculty of Biology, University of Vigo, 36310 Vigo (Spain).
Unit of Interventional Bronchopleural Pathology, Pneumology Department of Hospital University Complex of Vigo (CHUVI), 36214 Vigo (Spain).
Sci Rep. 2014 Feb 6;4:3999. doi: 10.1038/srep03999.
In this study, we measured ADA and DPP-IV enzymatic activity and sCD26 concentration in 150 pleural effusion (PE) samples and tested for correlations between these and other cellular and biochemical measures. We found that DPP-IV in particular might improve the specificity (but not the sensitivity) of the ADA test for diagnosis of pulmonary tuberculosis, since half of the false ADA positive results in non-tuberculous PE were also DPP-IV positive. A percentage of patients with malignant PE were sCD26 or DPP-IV positive; however, some patients with benign PE also tested positive. As a pattern associated with DPP-IV (but not the CD26 protein) was observed in PE, we searched for a finding that might increase the value of these biomarkers for diagnosis of malignancy. The observed pattern was related to the presence of leukocytes, as indicated by correlations with the cell count, and to a band of 180 kDa, detected by immunoblotting.
在这项研究中,我们测量了 150 份胸腔积液 (PE) 样本中的 ADA 和 DPP-IV 酶活性以及 sCD26 浓度,并测试了这些与其他细胞和生化指标之间的相关性。我们发现,DPP-IV 特别可能提高 ADA 检测对肺结核诊断的特异性(但不提高其敏感性),因为在非结核性 PE 中,一半 ADA 假阳性结果也是 DPP-IV 阳性。一部分恶性 PE 患者 sCD26 或 DPP-IV 阳性;然而,一些良性 PE 患者也检测为阳性。由于在 PE 中观察到与 DPP-IV(而不是 CD26 蛋白)相关的模式,我们寻找可能增加这些生物标志物用于诊断恶性肿瘤的价值的发现。观察到的模式与白细胞的存在有关,如与细胞计数的相关性所表明的,并且与免疫印迹检测到的 180 kDa 条带有关。