原发性和继发性肾小球肾炎的t淋巴细胞亚群。

A Fornasieri, R Sinico, G Fiorini, D Goldaniga, G Colasanti, F Vendemia, A Gibelli, G D'Amico
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引用次数: 0

摘要

使用单克隆抗体OKT3(外周t细胞)、OKT4(辅助/诱导t细胞)和OKT8(抑制/细胞毒性t细胞)在110例原发性和继发性肾小球肾炎(伯杰病、膜性肾小球肾炎、局灶性肾小球硬化、膜增生性肾炎、狼疮性肾炎和混合必需性冷球蛋白血症)患者的外周血中测定t淋巴细胞亚群。我们发现Berger’s病和膜性GN患者OKT4+/OKT8+比值明显较高,而狼疮肾炎和混合性必需性冷球蛋白血症患者OKT4+/OKT8+比值较低,这是由于OKT4+细胞明显减少所致。我们的结果表明在某些形式的GN中存在免疫调节机制的不平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-lymphocyte subsets in primary and secondary glomerulonephritis.

T-lymphocyte subsets, using the monoclonal antibodies OKT3 (peripheral T-cells), OKT4 (helper/inducer T-cells) and OKT8 (suppressor/cytotoxic T-cells) were measured in peripheral blood from 110 patients with various forms of primary and secondary glomerulonephritis (GN) (Berger's disease, membranous GN, focal glomerulosclerosis, membranoproliferative GN, lupus nephritis and mixed essential cryoglobulinaemia with GN). We have found a significantly higher OKT4+/OKT8+ ratio in patients with Berger's disease and membranous GN and a rather low OKT4+/OKT8+ ratio in patients with lupus nephritis and mixed essential cryoglobulinaemia, due to a significant decrease in OKT4+ cells. Our results suggest an imbalance in immunoregulatory mechanisms in some forms of GN.

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