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原发性胆汁性肝硬化中的淋巴细胞毒性抗体。

Lymphocytotoxic antibodies in primary biliary cirrhosis.

作者信息

Parés A, Martorell J, Caballería J, Vives J, Bruguera M, Rodés J

出版信息

Dig Dis Sci. 1985 Sep;30(9):829-33. doi: 10.1007/BF01309512.

Abstract

Sera of 30 patients with primary biliary cirrhosis (PBC) and 72 normal subjects matched for age and sex were examined for the presence of lymphocytotoxic antibodies (LCAs) against B and T cells at 4 degrees C and 37 degrees C. Patients were prospectively screened for: Sjögren's syndrome, scleroderma, Hashimoto's thyroiditis, and rheumatoid arthritis, in which LCAs have been described. Seventeen patients with PBC (56.6%) had LCAs against B cells as compared with only 11 of the 72 normal subjects (P less than 0.001). Five PBC patients (16.6%) also reacted against T cells as compared with none in control group (P less than 0.01). Clinical and biochemical features and the histological stage of PBC were similar in patients with and without LCA. Sjögren's syndrome was present in 13 patients--two with scleroderma and another with Hashimoto's thyroiditis. No patient had rheumatoid arthritis. The prevalence of LCAs was similar in PBC patients with or without autoimmune associated disease (54% vs 59%). We conclude that in PBC a high incidence of LCA is unrelated to the presence of an associated disease. LCA in PBC might be a nonspecific marker of an immune disorder.

摘要

对30例原发性胆汁性肝硬化(PBC)患者以及72例年龄和性别相匹配的正常受试者的血清进行检测,以确定在4℃和37℃时针对B细胞和T细胞的淋巴细胞毒性抗体(LCA)的存在情况。对患者进行前瞻性筛查,以确定是否患有干燥综合征、硬皮病、桥本甲状腺炎和类风湿关节炎,这些疾病中已报道存在LCA。17例PBC患者(56.6%)存在针对B细胞的LCA,而72例正常受试者中只有11例(P<0.001)。5例PBC患者(16.6%)也对T细胞产生反应,而对照组无一例出现这种情况(P<0.01)。有LCA和无LCA的PBC患者的临床和生化特征以及PBC的组织学分期相似。13例患者患有干燥综合征,其中2例合并硬皮病,另1例合并桥本甲状腺炎。无患者患有类风湿关节炎。有或无自身免疫相关疾病的PBC患者中LCA的患病率相似(54%对59%)。我们得出结论,在PBC中,LCA的高发生率与相关疾病的存在无关。PBC中的LCA可能是免疫紊乱的非特异性标志物。

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