Schiavino D, Sasso F, Nucera E, Alcini E, Gulino G, Milani A, Patriarca G
Department of Internal Medicine, University Cattolica S. Cuore of Rome, Italy.
Urology. 1997 Nov;50(5):764-8. doi: 10.1016/S0090-4295(97)00333-6.
Recent literature suggests the hypothesis of an immune etiology of Peyronie's disease. In this controlled study, the immune response pattern of the disease is investigated.
Sixty-six patients with Peyronie's disease and 20 age-matched controls were studied. In all patients, skin test (multitest), in vitro lymphocyte transformation test (LTT), serum immunoglobulin (Ig) A, G, and M, anti-DNA, antinuclear and anti-smooth muscle cell antibodies, C3 and C4 complement fractions, antistreptolysin, and C-reactive protein titers were evaluated.
A fair percentage (75.8%) of the patients with Peyronie's disease exhibited at least one abnormal immunologic test, in comparison to only 10% among controls (chi-square = 27.8, df = 1; P < 0.0001). Alterations of cell-mediated immunity (multitest, LTT) were observed in 48.5% of patients, alterations of humoral immunity (Ig) in 31.8%, and alterations of markers of autoimmune disorders (autoantibodies, complement activation) in 37.9% of the cases.
Our results support the hypothesis that there is some involvement of the immune system in the pathogenesis of Peyronie's disease, although the available data still appear to be insufficient to formulate a definite pathogenetic hypothesis.
近期文献提出佩罗尼氏病存在免疫病因的假说。在这项对照研究中,对该疾病的免疫反应模式进行了调查。
对66例佩罗尼氏病患者和20例年龄匹配的对照者进行了研究。对所有患者评估了皮肤试验(多项试验)、体外淋巴细胞转化试验(LTT)、血清免疫球蛋白(Ig)A、G和M、抗DNA、抗核和抗平滑肌细胞抗体、C3和C4补体成分、抗链球菌溶血素以及C反应蛋白滴度。
佩罗尼氏病患者中有相当比例(75.8%)至少有一项免疫学检查异常,而对照组中这一比例仅为10%(卡方 = 27.8,自由度 = 1;P < 0.0001)。48.5%的患者观察到细胞介导免疫(多项试验、LTT)改变,31.8%的患者观察到体液免疫(Ig)改变,37.9%的病例观察到自身免疫性疾病标志物(自身抗体、补体激活)改变。
我们的结果支持免疫系统在佩罗尼氏病发病机制中存在某种参与的假说,尽管现有数据似乎仍不足以形成明确的发病机制假说。