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Serum proteins in chronic hepatitis B patients treated with peginterferon alfa-2b
Authors:Sunida Kuakarn,  Poorichaya SomParn,  Pisit Tangkijvanich,  Varocha Mahachai,  Visith Thongboonkerd,  Nattiya Hirankarn
Affiliation:[1]Medical Microbiology, Interdisciplinary Program, Graduate School, Chulalongkorn University, Bangkok 10330, Thailand; [2]Immunology Unit,Department of Microbiology, Faculty of Medicine, Chulalong-korn University, Bangkok 10330, Thailand; [3]Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand; [4]Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand; [5]Medical Proteomics Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital,Mahidol University, Bangkok 10700, Thailand; [6]Center for Research in Complex Systems Science, Mahidol University, Bangkok 10700, Thailand
Abstract:AIM: To study the differential protein profile in serum of hepatitis B patients.METHODS: Serum samples were obtained from patients with chronic hepatitis B who were receiving peginterferon alfa-2b. The serum samples were subjected to albumin depletion and analyzed by two-dimensional gel electrophoresis (2-DE). Differentially expressed protein spots were identified by electrospray ionization-quadrupole time-of-flight mass spectrometry. Alpha-2-HS-glycoprotein, complement component C3c and CD5 antigen were further analyzed by an enzyme-linked immunosorbent assay and immunonephelometry.RESULTS: Nineteen patients with HBeAg-positive chronic hepatitis B (CHB) were studied. These patients were followed for at least 1 year after treatment and were classified according to their treatment response: responders (n = 9) and non-responders (n = 10). 2-DE and MS/MS analysis were performed to compare the serum proteins before initiating peginterferon alfa-2b. From the quantitative analysis of the 2-D gel, 7 proteins were detected between the two groups at different levels before treatment. Among these potential candidates, serum levels of alpha-2-HS-glycoprotein, complement component C3c and CD5 antigen-like precursor were further analyzed. In the validation phase, 23 subjects, 9 sustained responders and 14 non-responders, were recruited. Interestingly, the levels of alpha-2-HS-glycoprotein and complement component C3c were elevated in the serum of the non-responders compared to the responders.CONCLUSION: Serum alpha-2-HS-glycoprotein and complement component C3c may be potential serum biomarkers in predicting the treatment response of peginterferon alfa-2b in patients with CHB prior to treatment.
Keywords:Proteomics   Peginterferon alfa-2b   Chronic hepatitis B   Alpha-2-HS-glycoprotein   Serum
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