• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

15-脱氧精胍菌素(DSG)对大鼠同种异体肾移植的影响:与长期存活相关的免疫机制

Effect of 15-deoxyspergualin (DSG) on rat kidney allograft: immunological mechanisms implicated in prolonged survival.

作者信息

Chikaraishi T, Ishikura H, Seki T, Koyanagi T, Yoshiki T

机构信息

Department of Urology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

J Urol. 1995 Dec;154(6):2197-202.

PMID:7500488
Abstract

PURPOSE AND METHODS

The effect of short-term administration of 15-deoxyspergualin (DSG), 5 mg./kg./day from postoperative days 4 to 7, on rat renal transplantation was studied.

RESULTS

Although allografts treated with DSG survived longer than nontreated ones, cellular infiltration in both grafts did not differ. However, renal tubular cells of DSG-treated grafts proliferated well and escaped apoptotic cell death. A donor-specific tolerance 2 weeks after transplantation was developed, and cells with in vitro suppressor function were induced in such animals.

CONCLUSIONS

Treatment with DSG appears to prevent lethal attack of effector cells on tubular cells in situ and to generate suppressor cells in the maintenance phase of graft enhancement.

摘要

目的与方法

研究术后第4天至第7天每天给予15 - 去氧精胍菌素(DSG)5毫克/千克对大鼠肾移植的影响。

结果

虽然用DSG处理的同种异体移植物存活时间比未处理的长,但两种移植物中的细胞浸润没有差异。然而,用DSG处理的移植物的肾小管细胞增殖良好,未发生凋亡性细胞死亡。移植后2周形成了供体特异性耐受,并且在这类动物中诱导出具有体外抑制功能的细胞。

结论

DSG治疗似乎可防止效应细胞对原位肾小管细胞的致命攻击,并在移植物增强的维持阶段产生抑制细胞。

相似文献

1
Effect of 15-deoxyspergualin (DSG) on rat kidney allograft: immunological mechanisms implicated in prolonged survival.15-脱氧精胍菌素(DSG)对大鼠同种异体肾移植的影响:与长期存活相关的免疫机制
J Urol. 1995 Dec;154(6):2197-202.
2
Possible mechanism in rat with surviving heart allograft after short course of 15-deoxyspergualin treatment.
J Clin Lab Immunol. 1990 Jul;32(3):131-6.
3
The immunopharmacology of immunosuppression by 15-deoxyspergualin.15-脱氧精胍菌素免疫抑制的免疫药理学
Transplantation. 1993 Mar;55(3):578-91. doi: 10.1097/00007890-199303000-00023.
4
Immunological analysis of rat renal transplant recipients exhibiting long-term survival following treatment with 15-deoxyspergualin in the early postoperative phase.对术后早期用15-去氧精胍菌素治疗后表现出长期存活的大鼠肾移植受者的免疫学分析。
Int J Urol. 1998 Sep;5(5):476-81. doi: 10.1111/j.1442-2042.1998.tb00393.x.
5
Synergistic effect of donor-specific blood transfusion and a short course of deoxyspergualin in rat kidney transplantation.
Transpl Int. 1996;9(4):353-8. doi: 10.1007/BF00335694.
6
Peritransplant tolerance induction in macaques: early events reflecting the unique synergy between immunotoxin and deoxyspergualin.猕猴移植耐受诱导:反映免疫毒素与脱氧精胍菌素独特协同作用的早期事件
Transplantation. 1999 Dec 15;68(11):1660-73. doi: 10.1097/00007890-199912150-00009.
7
DNA nick end labeling of rat renal allografts treated with 15-deoxyspergualin (DSG).用15-去氧精胍菌素(DSG)处理的大鼠同种异体肾移植的DNA缺口末端标记
Transplant Proc. 1995 Feb;27(1):557-8.
8
Cellular mechanisms: induction of heart allograft survival in rats by 15-deoxyspergualin.细胞机制:15-脱氧精胍菌素诱导大鼠心脏同种异体移植物存活
Transpl Int. 1992;5 Suppl 1:S497-500. doi: 10.1007/978-3-642-77423-2_146.
9
In vivo and in vitro mechanisms of cardiac allograft acceptance in the rat after short treatment with 15-deoxyspergualin.大鼠经15-脱氧精胍菌素短期处理后心脏同种异体移植接受的体内和体外机制
Transpl Int. 1992 Jul;5(3):139-44. doi: 10.1007/BF00336598.
10
Effect of FK-506 on heart allograft survival in the highly sensitized recipient rats as compared with ciclosporin and 15-deoxyspergualin.与环孢素和15-去氧精胍菌素相比,FK-506对高敏受者大鼠心脏同种异体移植存活的影响。
Eur Surg Res. 1991;23(3-4):201-5. doi: 10.1159/000129153.

引用本文的文献

1
Induction of transplantation tolerance in non-human primate preclinical models.非人灵长类动物临床前模型中移植耐受的诱导
Philos Trans R Soc Lond B Biol Sci. 2005 Sep 29;360(1461):1723-37. doi: 10.1098/rstb.2005.1703.