Hyla-Klekot Lidia, Kucharska Grazyna, Cieślak Witold, Siekiera Urszula, Pulcer Barbara
Z Chorzowskiego Centrum Pediatrii i Onkologii.
Wiad Lek. 2005;58 Suppl 1:45-9.
In this study a genetic determination of some cytokines synthesis is presented in group of 23 children with various kinds of nephrotic syndrome (NS). The gene polymorphisms of TNF-alpha, TGF-beta, IL-6, IL-10, INF-gamma were identified using PCR-SSP method combined with the measurement of levels of TNF-alpha, TGF-beta, IL-6, IL-10, INF-gamma synthesis. The differences in occurring frequency of high, middle and low genotypes TNF-alpha, TGF-beta and IL-6 synthesis between children with NS and control group were revealed. Significantly more frequently high TGF-beta and high IL-6 synthesis genotype in NS group were found. Because of high variability of cytokine level in blood in duration of NS and methodic difficulties of their measurement, identification of cytokines genes polymorphisms seems to be a method that can objectively describe the cytokine participation in NS pathophysiology.
本研究对23名患有各种类型肾病综合征(NS)的儿童进行了某些细胞因子合成的基因测定。采用PCR-SSP方法结合TNF-α、TGF-β、IL-6、IL-10、INF-γ合成水平的测定,鉴定了TNF-α、TGF-β、IL-6、IL-10、INF-γ的基因多态性。揭示了NS患儿与对照组之间TNF-α、TGF-β和IL-6合成的高、中、低基因型出现频率的差异。发现NS组中高TGF-β和高IL-6合成基因型的出现频率明显更高。由于NS病程中血液中细胞因子水平的高度变异性及其测量的方法学困难,细胞因子基因多态性的鉴定似乎是一种能够客观描述细胞因子参与NS病理生理学的方法。