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Spleen lymphocyte populations and expression of activation markers in rats treated with the potent new immunosuppressive agent FK-506.

机译:用强效新型免疫抑制剂FK-506处理的大鼠的脾脏淋巴细胞群和激活标记物的表达。

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摘要

Rats were immunized systemically with sheep red blood cells (SRBC) and treated with either FK-506 (1 mg/kg/day) or cyclosporin A (CsA) (25 mg/kg/day) for 7 days. Profound (greater than 90%) suppression of the production of splenic IgM-secreting plasma cells and circulating antibody levels was observed in animals receiving either drug. Immunosuppression was accompanied by significant increases in the incidence and absolute numbers of OX8+ (T-cytotoxic/suppressor) lymphocytes in the spleen, and there were corresponding reductions in the W3/25+:OX8 (CD4+:CD8+) ratio. The magnitude of these changes was not affected by drug combination. There were no significant alterations in B cells with either agent, whilst a small but significant increase in the incidence of macrophages was observed in all drug-treated groups. Neither FK-506 nor CsA affected IL-2 receptor (OX39) or MHC class II (OX6) antigen expression. This study demonstrates the remarkable immunosuppressive potency of FK-506 and its underlying capacity, like CsA, to affect regulatory T-lymphocyte subsets in vivo.
机译:用绵羊红细胞(SRBC)全身免疫大鼠,并用FK-506(1 mg / kg /天)或环孢菌素A(CsA)(25 mg / kg /天)处理7天。在接受这两种药物的动物中,均观察到了对脾脏分泌IgM分泌浆细胞产量和循环抗体水平的深刻抑制(大于90%)。免疫抑制伴随着脾脏中OX8 +(T细胞毒性/抑制剂)淋巴细胞的发生率和绝对数量显着增加,并且W3 / 25 +:OX8(CD4 +:CD8 +)比例相应降低。这些变化的幅度不受药物组合的影响。两种药物在B细胞中均无明显变化,而在所有药物治疗组中,巨噬细胞的发生率均出现小幅但显着的增加。 FK-506和CsA均不影响IL-2受体(OX39)或MHC II类(OX6)抗原表达。这项研究证明了FK-506的显着免疫抑制能力及其潜在能力(如CsA)在体内影响调节性T淋巴细胞亚群。

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