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通过SOAz(一种环磷腈衍生药物)对淋巴细胞多克隆激活进行体内调节。预防慢性注射脂多糖诱导的小鼠肾小球肾炎。

In vivo modulation of polyclonal activation of lymphocytes by SOAz, a cyclophosphazene derived drug. Prevention of murine glomerulonephritis induced by chronic injections of lipopolysaccharide.

作者信息

Dueymes M, Fournie G J, Carentz F, Mignon-Conte M, Labarre J F, Conte J J

出版信息

Clin Exp Immunol. 1985 Jan;59(1):169-76.

Abstract

The effects of a cyclophosphazene derived drug (SOAz), on the polyclonal activation of B lymphocytes induced by bacterial lipopolysaccharide (LPS) have been studied in C57B1/6 mice. It has been found that this drug is able to inhibit the polyclonal stimulation of lymphocytes and a dose-dependent effect has been observed. The therapeutic effects of SOAz injected five times a week at 40 mg/kg/day have been investigated in mice chronically injected with LPS (twice a week, 2.5 mg/kg/day) which developed an immune complex type of glomerulonephritis. A marked prevention of glomerular lesions and of deposits of IgM and IgG, and of the third complement component has been found in mice treated with SOAz as compared to not treated mice.

摘要

已在C57B1/6小鼠中研究了一种环磷腈衍生药物(SOAz)对细菌脂多糖(LPS)诱导的B淋巴细胞多克隆激活的影响。已发现该药物能够抑制淋巴细胞的多克隆刺激,并观察到剂量依赖性效应。在慢性注射LPS(每周两次,2.5mg/kg/天)并发展为免疫复合物型肾小球肾炎的小鼠中,研究了每周注射5次、剂量为40mg/kg/天的SOAz的治疗效果。与未治疗的小鼠相比,在用SOAz治疗的小鼠中发现肾小球病变以及IgM和IgG沉积以及第三补体成分有明显的预防作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cd6/1577161/604b2beb46df/clinexpimmunol00136-0183-a.jpg

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