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新型免疫抑制剂FK506可在活动性海曼肾炎及肾毒血清性肾炎自身期诱导抗原特异性免疫耐受。

FK506, a novel immunosuppressive agent, induces antigen-specific immunotolerance in active Heymann's nephritis and in the autologous phase of Masugi nephritis.

作者信息

Okubo Y, Tsukada Y, Maezawa A, Ono K, Yano S, Naruse T

机构信息

Third Department of Internal Medicine, Gunma University School of Medicine, Japan.

出版信息

Clin Exp Immunol. 1990 Dec;82(3):450-5. doi: 10.1111/j.1365-2249.1990.tb05470.x.

Abstract

FK506 is a new drug which has potent immunosuppressive activity. We studied its immunosuppressive effects on active Heymann's nephritis and the autologous phase of Masugi nephritis. The induction of active Heymann's nephritis was completely suppressed by FK506 injected simultaneously with the antigen (day 1) and then daily for 14 days at a dose of 0.64 mg/kg per day or more. With a lower dosage of this agent, antibody production and immune deposits in the glomerular basement membrane occurred despite the suppression of proteinuria. Similar results were obtained in rats on other treatment schedules (1-7 days or day 8-14 days duration). Rats that were prevented from developing Heymann's nephritis or the autologous phase of nephrotoxic antiserum nephritis by FK506 treatment exhibited a suppressed immune response to a second immunization of the same antigen even 4 weeks after cessation of drug administration: however, they developed antibodies when inoculated with other antigens. Rat peripheral leucocyte counts and serum creatinin were not remarkably influenced by the administration of FK506. These results indicate that FK506 has potent immunosuppressive activity, and it is suggested that it is able to induce an antigen-specific immunotolerance.

摘要

FK506是一种具有强大免疫抑制活性的新药。我们研究了它对活动性海曼肾炎和马苏吉肾炎自身期的免疫抑制作用。同时注射FK506与抗原(第1天),然后每天以0.64毫克/千克或更高剂量连续注射14天,可完全抑制活动性海曼肾炎的诱发。使用较低剂量的该药物时,尽管蛋白尿得到抑制,但肾小球基底膜中仍会出现抗体产生和免疫沉积物。在其他治疗方案(持续1 - 7天或8 - 14天)的大鼠中也获得了类似结果。通过FK506治疗预防了海曼肾炎或肾毒性抗血清肾炎自身期发展的大鼠,即使在停药4周后,对相同抗原的第二次免疫仍表现出免疫反应受抑制;然而,当接种其他抗原时,它们会产生抗体。给予FK506对大鼠外周白细胞计数和血清肌酐没有显著影响。这些结果表明FK506具有强大的免疫抑制活性,并且提示它能够诱导抗原特异性免疫耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ba5/1535500/03995d55f90c/clinexpimmunol00069-0034-a.jpg

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