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Differential expression of immune factor between patients with chronic prostatitis/chronic pelvic pain syndrome and the healthy volunteers

机译:慢性前列腺炎/慢性盆腔疼痛综合征和健康志愿者患者免疫因子的差异表达

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Abstract Purpose Immune mechanisms have been hypothesized to contribute to the development of CP/CPPS. In this study, we investigated the differential expression of immune factors between patients with CP/CPPS and healthy volunteers. Methods This study was registered in Australian New Zealand Clinical Trials Registry. Healthy volunteers and patients with CP/CPPS were enrolled in this study. The inclusion criteria for patients were below: (1) aged 18–45?years old; (2) prostatitis-related syndrome longer than 3?months; (3) normal routine urine culture and negative bacterial culture in prostatic fluid. Patients were further classified into two groups: types IIIA and IIIB CP/CPPS according to the results of EPS routine test. Serum immune markers include IgA, IgM, IgG, CD4_(+)and CD8_(+). Results There are total 23 CP/CPPS patients, including 12 type IIIB and 11 type IIIA. Relatively, there are 26 healthy volunteers. The serum levels of IgG were higher in CP/CPPS patients compared to healthy volunteers (1141.2?±?204.3 vs 1031.9?±?173.7?mg/L, p ?=?0.045), while the serum levels of CD8_(+)were lower in CP/CPPS patients compared to healthy volunteers (492.8?±?185.6 vs 640.0?±?246.8 cells/μL, p ?=?0.021). Furthermore, serum levels of IgG were higher in patients with IIIA CP/CPPS compared to those with IIIB (1244.3?±?151.6 vs 1054.3?±?209.3?mg/L, p ?=?0.023). Conclusions Differential levels of IgG and CD8_(+)between CPPS patients and healthy volunteers suggest a contributing role of immune mechanisms to the development of CP/CPPS; and IgG may play an important role in inflammatory CPPS. Clinical Study registration number ACTRN12613000792729.
机译:摘要目的免疫机制已被假设为促进CP / CPP的发展。在这项研究中,我们研究了CP / CPP和健康志愿者患者之间免疫因子的差异表达。方法本研究在澳大利亚新西兰临床试验登记处注册。本研究注册了健康的志愿者和CP / CPP的患者。含有患者的纳入标准低于:(1)年龄18-45岁?岁; (2)前列腺炎相关的综合征超过3?几个月; (3)前列腺液正常常规尿培养和负细菌培养。根据EPS常规测试的结果,患者进一步分为两组:IIIA型和IIIB CP / CPP。血清免疫标记包括IgA,IgM,IgG,CD4 _(+)和CD8 _(+)。结果总计23例CP / CPPS患者,其中包括12型IIIB和11型IIIA型。相对,有26个健康的志愿者。与健康的志愿者相比,CP / CPPS患者的IgG血清IgG水平较高(1141.2?±204.3 Vs 1031.9?±173.7毫克/升,P?= 0.045),而CD8 _(+)的血清水平是与健康志愿者相比,CP / CPPS患者中较低(492.8?±185.6 Vs 640.0?±246.8个细胞/μl,p?= 0.021)。此外,与IIIB的那些(1244.3?±151.6 vs 1054.3?±209.3×15 / l,p?= 0.023)相比,IIIa CP / CPP患者血清IgG水平较高。结论CPP患者和健康志愿者之间IgG和CD8 _(+)的差异水平表明免疫机制对CP / CPPS发展的贡献作用;并且IgG可能在炎症CPP中发挥重要作用。临床研究登记号码ACTRN12613000792729

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