• 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

脾切除对小鼠抵抗溶组织内阿米巴感染能力的影响。

The effect of splenectomy on resistance of mice to Entamoeba histolytica infection.

作者信息

Ghadirian E, Kongshavn P A

出版信息

Parasite Immunol. 1985 Sep;7(5):479-87. doi: 10.1111/j.1365-3024.1985.tb00093.x.

DOI:10.1111/j.1365-3024.1985.tb00093.x
PMID:2999680
Abstract

The role of the spleen in amoebic infection was examined in mice, using strains selected as being either genetically-susceptible (C57BL/6) or genetically-resistant (A/J) to amoebiasis. Splenectomized and sham-operated animals were inoculated intracaecally with 2.5 X 10(5) polyxenic trophozoites of E. histolytica at 6, 12 and 15 days post-splenectomy. The animals were killed 6 or 12 days after infection and the parasite burden was evaluated. Removal of the spleen in both susceptible and resistant mouse strains rendered these hosts extremely resistant to amoebic infection by this criterion. Gross examination of the caeca of non-splenectomized, genetically-susceptible mice showed numerous ulcers over the mucosal surface when compared to the splenectomized group which had superficial lesions or none. These observations suggest that the spleen plays a suppressive role in early anti-amoebic resistance.

摘要

利用对阿米巴病具有遗传易感性(C57BL/6)或遗传抗性(A/J)的品系小鼠,研究脾脏在阿米巴感染中的作用。在脾切除术后第6、12和15天,对脾切除和假手术的动物经盲肠内接种2.5×10⁵个溶组织内阿米巴多菌型滋养体。在感染后6天或12天处死动物,并评估寄生虫负荷。按照这一标准,切除易感和抗性小鼠品系的脾脏均使这些宿主对阿米巴感染具有极强的抗性。与有浅表病变或无病变的脾切除组相比,对未进行脾切除、具有遗传易感性的小鼠的盲肠进行大体检查发现,其粘膜表面有大量溃疡。这些观察结果表明,脾脏在早期抗阿米巴抗性中起抑制作用。

相似文献

1
The effect of splenectomy on resistance of mice to Entamoeba histolytica infection.脾切除对小鼠抵抗溶组织内阿米巴感染能力的影响。
Parasite Immunol. 1985 Sep;7(5):479-87. doi: 10.1111/j.1365-3024.1985.tb00093.x.
2
Effect of silica on resistance of mice to Entamoeba histolytica infection.二氧化硅对小鼠抵抗溶组织内阿米巴感染的影响。
Infect Immun. 1984 Aug;45(2):399-402. doi: 10.1128/iai.45.2.399-402.1984.
3
Immunosuppression and splenomegaly in Entamoeba histolytica infection in mice.小鼠溶组织内阿米巴感染中的免疫抑制和脾肿大
Microb Pathog. 1987 Apr;2(4):241-8. doi: 10.1016/0882-4010(87)90122-7.
4
Genetic control of susceptibility of mice to infection with E. histolytica.小鼠对溶组织内阿米巴感染易感性的遗传控制。
Parasite Immunol. 1984 Jul;6(4):349-60. doi: 10.1111/j.1365-3024.1984.tb00807.x.
5
Effect of specific and non-specific prior sensitization on the outcome of amoebic infection.特异性和非特异性预先致敏对阿米巴感染结果的影响。
Trans R Soc Trop Med Hyg. 1981;75(1):25-31. doi: 10.1016/0035-9203(81)90009-2.
6
Alterations of humoral, cell mediated and antibody dependent cell mediated cytotoxic responses during the course of amoebic infection in guinea pigs.豚鼠阿米巴感染过程中体液免疫、细胞介导免疫及抗体依赖性细胞介导的细胞毒性反应的变化
Gut. 1987 Oct;28(10):1251-6. doi: 10.1136/gut.28.10.1251.
7
Entamoeba histolytica: early progressive pathology in the cecum of the gerbil (Meriones unguiculatus).溶组织内阿米巴:沙土鼠(长爪沙鼠)盲肠的早期进行性病理变化
Am J Trop Med Hyg. 1985 Mar;34(2):283-91. doi: 10.4269/ajtmh.1985.34.283.
8
Experimental amoebic infection in guinea-pigs immunized with low grade amoebic infection.用轻度阿米巴感染免疫的豚鼠的实验性阿米巴感染。
Trans R Soc Trop Med Hyg. 1980;74(3):347-50. doi: 10.1016/0035-9203(80)90097-8.
9
Development of inflammation and augmented chemotactic responsiveness of murine peritoneal macrophages following treatment with Entamoeba histolytica trophozoites.
Microb Pathog. 1987 Sep;3(3):207-14. doi: 10.1016/0882-4010(87)90097-0.
10
Oral lactoferrin treatment resolves amoebic intracecal infection in C3H/HeJ mice.口服乳铁蛋白治疗可解决 C3H/HeJ 小鼠的肠内阿米巴感染。
Biochem Cell Biol. 2012 Jun;90(3):435-41. doi: 10.1139/o2012-008. Epub 2012 Mar 27.

引用本文的文献

1
Host-pathogen interaction in amebiasis and progress in vaccine development.阿米巴病中的宿主-病原体相互作用及疫苗研发进展
Eur J Clin Microbiol Infect Dis. 1998 Sep;17(9):601-14. doi: 10.1007/BF01708342.