The Possible Role of Interleukin (IL)-12 and Interferon-γ-Inducing Factor/IL-18 in Protection against ExperimentalMycobacterium lepraeInfection in Mice

Kazuo Kobayashi , Masanori Kai , Masa-ichi Gidoh , Noboru Nakata , Masumi Endoh , Ram Pyare Singh , Tsuyoshi Kasama , Hajime Saito
{"title":"The Possible Role of Interleukin (IL)-12 and Interferon-γ-Inducing Factor/IL-18 in Protection against ExperimentalMycobacterium lepraeInfection in Mice","authors":"Kazuo Kobayashi ,&nbsp;Masanori Kai ,&nbsp;Masa-ichi Gidoh ,&nbsp;Noboru Nakata ,&nbsp;Masumi Endoh ,&nbsp;Ram Pyare Singh ,&nbsp;Tsuyoshi Kasama ,&nbsp;Hajime Saito","doi":"10.1006/clin.1998.4533","DOIUrl":null,"url":null,"abstract":"<div><p>Cell-mediated immunity participates in host defense against mycobacterial infection. Both interleukin 12 (IL-12) and interferon-γ-inducing factor (IGIF/IL-18), produced mainly by macrophages, play a critical role in expression of cell-mediated immunity. To investigate the role of IL-12 and IGIF/IL-18<em>in vivo,</em>we examined cytokine profile, bacterial growth, and the potential benefit of cytokine therapy in susceptible and resistant mice infected with<em>Mycobacterium leprae.</em>The early expression of IL-12 p40 and IGIF/IL-18 at the site of inoculation was found in resistant mice 3–72 h after the infection, but not in susceptible mice. Both strains of mice did not show expression of IFN-γ and IL-4. IL-12 administration resulted in a significant reduction of bacterial counts in mice with established<em>M. leprae</em>infection. The results imply that susceptible mice exhibit decreased expression of type 1 helper T (Th1) response without reciprocal increased Th2 response and show responsiveness to exogenous IL-12. IL-12 therapy may be a possible rationale for treatment of<em>M. leprae</em>infection.</p></div>","PeriodicalId":10683,"journal":{"name":"Clinical immunology and immunopathology","volume":"88 3","pages":"Pages 226-231"},"PeriodicalIF":0.0000,"publicationDate":"1998-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/clin.1998.4533","citationCount":"80","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical immunology and immunopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0090122998945330","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 80

Abstract

Cell-mediated immunity participates in host defense against mycobacterial infection. Both interleukin 12 (IL-12) and interferon-γ-inducing factor (IGIF/IL-18), produced mainly by macrophages, play a critical role in expression of cell-mediated immunity. To investigate the role of IL-12 and IGIF/IL-18in vivo,we examined cytokine profile, bacterial growth, and the potential benefit of cytokine therapy in susceptible and resistant mice infected withMycobacterium leprae.The early expression of IL-12 p40 and IGIF/IL-18 at the site of inoculation was found in resistant mice 3–72 h after the infection, but not in susceptible mice. Both strains of mice did not show expression of IFN-γ and IL-4. IL-12 administration resulted in a significant reduction of bacterial counts in mice with establishedM. lepraeinfection. The results imply that susceptible mice exhibit decreased expression of type 1 helper T (Th1) response without reciprocal increased Th2 response and show responsiveness to exogenous IL-12. IL-12 therapy may be a possible rationale for treatment ofM. lepraeinfection.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
白细胞介素(IL)-12和干扰素-γ诱导因子/IL-18在小鼠实验性麻风分枝杆菌感染中的可能作用
细胞介导的免疫参与宿主对分枝杆菌感染的防御。白细胞介素12 (IL-12)和干扰素γ诱导因子(IGIF/IL-18)主要由巨噬细胞产生,在细胞介导免疫的表达中起关键作用。为了研究IL-12和IGIF/ il -18在体内的作用,我们检测了感染麻风分枝杆菌的易感和耐药小鼠的细胞因子谱、细菌生长以及细胞因子治疗的潜在益处。感染后3 ~ 72 h,耐药小鼠接种部位IL-12 p40和IGIF/IL-18均有早期表达,而易感小鼠无。两株小鼠均未显示IFN-γ和IL-4的表达。IL-12给药可显著减少小鼠的细菌计数。lepraeinfection。结果表明,易感小鼠表现出1型辅助性T (Th1)反应的表达降低,而Th2反应没有相应的增加,并对外源性IL-12表现出应答性。IL-12治疗可能是治疗多发性硬化症的基本原理。lepraeinfection。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Lymphotactin. Somatic Hypermutation in T-Independent and T-Dependent Immune Responses toHaemophilus influenzaeType b Polysaccharide CD8+, Radiosensitive T Cells of Parental Origin, Oppose Cells Capable of Down-Regulating Cytotoxicity in Murine Acute Lethal Graft-versus-Host Disease Characterization of Gastric Na+/I−Symporter of the Rat d-Penicillamine-Induced Pancreatic Islet Autoantibody Production Is Independent of the Immunogenetic Background: A Lesson from Patients with Wilson's Disease
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1