可溶性CD16在小鼠狼疮性肾炎治疗中的作用

Hiroshi Watanabe , David Sherris , Gary S. Gilkeson
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引用次数: 13

摘要

为了确定可溶性CD16 (sCD16)是否能改变狼疮样疾病的表达,10只雌性NZB/NZW小鼠(16-20周龄)每周给予3次sCD16,持续5周(对照组;100μg;200 μg/剂量)。本研究结果表明,在发病后给药sCD16可降低抗dna水平,延缓蛋白尿的发生,显著延长小鼠的生存期。这些结果表明,sCD16改变了NZB/NZW小鼠自身抗体的表达和肾脏疾病的进展,表明针对Fc受体的治疗可能对SLE的治疗有用。
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Soluble CD16 in the Treatment of Murine Lupus Nephritis

To determine if soluble CD16 (sCD16) could alter the expression of lupus-like disease, groups of 10 female NZB/NZW mice (age 16–20 weeks) were given sCD16 three times a week for 5 weeks (control; 100 μg; 200 μg/dose) after onset of proteinuria. Results of this study indicate that the administration of sCD16 after onset of disease lowered anti-DNA levels, delayed the development of proteinuria, and significantly prolonged survival while the mice were on treatment. These results indicate that sCD16 alters the expression of autoantibodies and the progression of renal disease in NZB/NZW mice, suggesting that therapies directed at Fc receptors may be useful in the treatment of SLE.

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