• 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

相似文献

1
The local immune response in ulcerative lesions of Buruli disease.布鲁里溃疡病溃疡性病变中的局部免疫反应。
Clin Exp Immunol. 2006 Mar;143(3):445-51. doi: 10.1111/j.1365-2249.2006.03020.x.
2
Cytokine response to antigen stimulation of whole blood from patients with Mycobacterium ulcerans disease compared to that from patients with tuberculosis.与结核病患者相比,溃疡分枝杆菌病患者全血对抗原刺激的细胞因子反应。
Clin Vaccine Immunol. 2006 Feb;13(2):253-7. doi: 10.1128/CVI.13.2.253-257.2006.
3
Local activation of the innate immune system in Buruli ulcer lesions.布鲁里溃疡病灶中固有免疫系统的局部激活。
J Invest Dermatol. 2007 Mar;127(3):638-45. doi: 10.1038/sj.jid.5700593. Epub 2006 Oct 19.
4
Differential production of systemic and intralesional gamma interferon and interleukin-10 in nodular and ulcerative forms of Buruli disease.布氏杆菌病结节型和溃疡型中全身及病灶内γ干扰素和白细胞介素-10的差异产生
Infect Immun. 2004 Feb;72(2):958-65. doi: 10.1128/IAI.72.2.958-965.2004.
5
Reduced apoptosis and increased inflammatory cytokines in granulomas caused by tuberculous compared to non-tuberculous mycobacteria: role of MPT64 antigen in apoptosis and immune response.与非结核分枝杆菌相比,结核分枝杆菌引起的肉芽肿中细胞凋亡减少且炎性细胞因子增加:MPT64抗原在细胞凋亡和免疫反应中的作用
Clin Exp Immunol. 2007 Oct;150(1):105-13. doi: 10.1111/j.1365-2249.2007.03476.x. Epub 2007 Aug 17.
6
Phagocytosis of Mycobacterium ulcerans in the course of rifampicin and streptomycin chemotherapy in Buruli ulcer lesions.在布鲁里溃疡病变中利福平与链霉素化疗过程中溃疡分枝杆菌的吞噬作用
Br J Dermatol. 2009 Feb;160(2):273-83. doi: 10.1111/j.1365-2133.2008.08879.x. Epub 2008 Oct 22.
7
Systemic suppression of interferon-gamma responses in Buruli ulcer patients resolves after surgical excision of the lesions caused by the extracellular pathogen Mycobacterium ulcerans.在布氏杆菌溃疡患者中,由细胞外病原体溃疡分枝杆菌引起的病变经手术切除后,全身性干扰素-γ反应的抑制得以缓解。
J Leukoc Biol. 2006 Jun;79(6):1150-6. doi: 10.1189/jlb.1005581. Epub 2006 Mar 10.
8
Serologic response to culture filtrate antigens of Mycobacterium ulcerans during Buruli ulcer disease.布氏杆菌病期间对溃疡分枝杆菌培养滤液抗原的血清学反应
Emerg Infect Dis. 2000 Mar-Apr;6(2):158-64. doi: 10.3201/eid0602.000208.
9
High rates of apoptosis in human Mycobacterium ulcerans culture-positive buruli ulcer skin lesions.人溃疡分枝杆菌培养阳性的布氏杆菌溃疡皮肤病变中凋亡率较高。
Am J Trop Med Hyg. 2005 Aug;73(2):410-5.
10
Immune response to infection with Mycobacterium ulcerans.对溃疡分枝杆菌感染的免疫反应。
Infect Immun. 2001 Mar;69(3):1704-7. doi: 10.1128/IAI.69.3.1704-1707.2001.

引用本文的文献

1
Macrophage fate: to kill or not to kill?巨噬细胞的命运:杀还是不杀?
Infect Immun. 2024 Sep 10;92(9):e0047623. doi: 10.1128/iai.00476-23. Epub 2024 Jun 3.
2
A human model of Buruli ulcer: The case for controlled human infection and considerations for selecting a Mycobacterium ulcerans challenge strain.人体布鲁里溃疡模型:人为感染控制的案例和选择溃疡分枝杆菌挑战株的考虑因素。
PLoS Negl Trop Dis. 2023 Jun 29;17(6):e0011394. doi: 10.1371/journal.pntd.0011394. eCollection 2023 Jun.
3
Bacteria and macrophages in the tumor microenvironment.肿瘤微环境中的细菌与巨噬细胞。
Front Microbiol. 2023 Feb 7;14:1115556. doi: 10.3389/fmicb.2023.1115556. eCollection 2023.
4
Extracellular vesicle-mediated regulation of macrophage polarization in bacterial infections.细胞外囊泡介导的细菌感染中巨噬细胞极化的调控
Front Microbiol. 2022 Dec 22;13:1039040. doi: 10.3389/fmicb.2022.1039040. eCollection 2022.
5
Identification of potential candidate vaccines against based on the major facilitator superfamily transporter protein.基于主要易化超家族转运蛋白鉴定针对 的潜在候选疫苗。
Front Immunol. 2022 Nov 8;13:1023558. doi: 10.3389/fimmu.2022.1023558. eCollection 2022.
6
Membrane Active Immunomodulator As a Novel Therapy for an Infectious Bacterial Disease, Buruli Ulcer.膜活性免疫调节剂作为一种治疗感染性细菌病——布鲁里溃疡的新疗法。
In Vivo. 2022 Nov-Dec;36(6):2615-2629. doi: 10.21873/invivo.12996.
7
Mycolactone toxin induces an inflammatory response by targeting the IL-1β pathway: Mechanistic insight into Buruli ulcer pathophysiology.Mycolactone 毒素通过靶向 IL-1β 途径诱导炎症反应:对伯里溃疡发病机制的机制见解。
PLoS Pathog. 2020 Dec 18;16(12):e1009107. doi: 10.1371/journal.ppat.1009107. eCollection 2020 Dec.
8
Notch-1 Signaling Modulates Macrophage Polarization and Immune Defense against Infection in Inflammatory Diseases.Notch-1信号通路调节巨噬细胞极化及炎症性疾病中抗感染的免疫防御。
Microorganisms. 2020 Jul 5;8(7):1006. doi: 10.3390/microorganisms8071006.
9
M2-Polarized Macrophages Determine Human Cutaneous Lesions in Lacaziosis.M2 极化的巨噬细胞决定拉卡佐病的人类皮肤损伤。
Mycopathologia. 2020 Jun;185(3):477-483. doi: 10.1007/s11046-020-00450-z. Epub 2020 May 6.
10
Vaccine-Specific Immune Responses against Mycobacterium ulcerans Infection in a Low-Dose Murine Challenge Model.在低剂量小鼠挑战模型中针对溃疡分枝杆菌感染的疫苗特异性免疫反应。
Infect Immun. 2020 Feb 20;88(3). doi: 10.1128/IAI.00753-19.

本文引用的文献

1
Infection with Mycobacterium ulcerans induces persistent inflammatory responses in mice.溃疡分枝杆菌感染会在小鼠体内引发持续的炎症反应。
Infect Immun. 2005 Oct;73(10):6299-310. doi: 10.1128/IAI.73.10.6299-6310.2005.
2
Mycobacterium ulcerans toxic macrolide, mycolactone modulates the host immune response and cellular location of M. ulcerans in vitro and in vivo.溃疡分枝杆菌毒性大环内酯类物质麦角硫因内酯在体外和体内均可调节宿主免疫反应及溃疡分枝杆菌的细胞定位。
Cell Microbiol. 2005 Sep;7(9):1295-304. doi: 10.1111/j.1462-5822.2005.00557.x.
3
Modulation of the host immune response by a transient intracellular stage of Mycobacterium ulcerans: the contribution of endogenous mycolactone toxin.溃疡分枝杆菌短暂胞内阶段对宿主免疫反应的调节:内源性分枝杆菌内酯毒素的作用
Cell Microbiol. 2005 Aug;7(8):1187-96. doi: 10.1111/j.1462-5822.2005.00546.x.
4
Colonization of the salivary glands of Naucoris cimicoides by Mycobacterium ulcerans requires host plasmatocytes and a macrolide toxin, mycolactone.溃疡分枝杆菌在黄斑仰蝽唾液腺中的定殖需要宿主的浆细胞和一种大环内酯毒素——分枝杆菌内酯。
Cell Microbiol. 2005 Jul;7(7):935-43. doi: 10.1111/j.1462-5822.2005.00521.x.
5
Differential production of systemic and intralesional gamma interferon and interleukin-10 in nodular and ulcerative forms of Buruli disease.布氏杆菌病结节型和溃疡型中全身及病灶内γ干扰素和白细胞介素-10的差异产生
Infect Immun. 2004 Feb;72(2):958-65. doi: 10.1128/IAI.72.2.958-965.2004.
6
Giant plasmid-encoded polyketide synthases produce the macrolide toxin of Mycobacterium ulcerans.巨大质粒编码的聚酮合酶产生溃疡分枝杆菌的大环内酯毒素。
Proc Natl Acad Sci U S A. 2004 Feb 3;101(5):1345-9. doi: 10.1073/pnas.0305877101. Epub 2004 Jan 21.
7
Immunology of tuberculosis and implications in vaccine development.结核病免疫学及其在疫苗研发中的意义。
Tuberculosis (Edinb). 2004;84(1-2):93-101. doi: 10.1016/j.tube.2003.08.010.
8
Histopathologic features of Mycobacterium ulcerans infection.溃疡分枝杆菌感染的组织病理学特征。
Emerg Infect Dis. 2003 Jun;9(6):651-656. doi: 10.3201/eid0906.020485.
9
Acquired T-helper 1 lymphocyte anergy following infection with Mycobacterium ulcerans.
Clin Infect Dis. 2003 Apr 15;36(8):1076-7. doi: 10.1086/368315. Epub 2003 Apr 3.
10
Expression of transforming growth factor-beta isoforms and their receptors in lepromatous and tuberculoid leprosy.转化生长因子-β亚型及其受体在瘤型和结核样型麻风病中的表达
Scand J Immunol. 2003 Mar;57(3):279-85. doi: 10.1046/j.1365-3083.2003.01210.x.

布鲁里溃疡病溃疡性病变中的局部免疫反应。

The local immune response in ulcerative lesions of Buruli disease.

作者信息

Kiszewski A E, Becerril E, Aguilar L D, Kader I T A, Myers W, Portaels F, Hernàndez Pando R

机构信息

Experimental Pathology Section, Department of Pathology, Salvador Zubiràn National Institute of Medical Sciences and Nutrition, Vasco de Quiroga 15, Tlalpan, Mexico City CP-14000, Mexico.

出版信息

Clin Exp Immunol. 2006 Mar;143(3):445-51. doi: 10.1111/j.1365-2249.2006.03020.x.

DOI:10.1111/j.1365-2249.2006.03020.x
PMID:16487243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1809619/
Abstract

Buruli disease (BU) is a progressive necrotic and ulcerative disease of the skin and subcutaneous tissue caused by Mycobacterium ulcerans. BU is considered the third most common mycobacterial disease after tuberculosis and leprosy. Three clinical stages of the cutaneous lesions have been described in BU: pre-ulcerative, ulcerative and healed lesions. In this study we used immunohistochemistry and automated morphometry to determine the percentage of macrophages and of CD4/CD8 lymphocytes and their expression of interferon (IFN)-gamma, interleukin (IL)-10, tumour necrosis factor (TNF)-alpha and transforming growth factor (TGF)-beta. Expression of these cytokines was correlated with the inflammatory response evaluated by histopathology. All the studied BU ulcerative cases showed extensive necrosis and chronic inflammation. The most important feature was the presence or absence of granulomas co-existing with a mixed pro-inflammatory/anti-inflammatory cytokine balance. When granulomas were present significantly higher expression of IFN-gamma was seen, whereas in ulcerative lesions without granulomas there was increased expression of IL-10 and significantly higher bacillary counts. These features correlated with the chronicity of the lesions; longer-lasting lesions showed granulomas. Thus, granulomas were absent from relatively early ulcerative lesions, which contained more bacilli and little IFN-gamma, suggesting that at this stage of the disease strong suppression of the protective cellular immune response facilitates proliferation of bacilli.

摘要

布鲁里溃疡(BU)是由溃疡分枝杆菌引起的一种皮肤和皮下组织的进行性坏死性和溃疡性疾病。布鲁里溃疡被认为是继结核病和麻风病之后的第三大常见分枝杆菌病。布鲁里溃疡的皮肤病变有三个临床阶段:溃疡前期、溃疡期和愈合期。在本研究中,我们使用免疫组织化学和自动形态测量法来确定巨噬细胞以及CD4/CD8淋巴细胞的百分比及其干扰素(IFN)-γ、白细胞介素(IL)-10、肿瘤坏死因子(TNF)-α和转化生长因子(TGF)-β的表达。这些细胞因子的表达与通过组织病理学评估的炎症反应相关。所有研究的布鲁里溃疡病例均显示广泛坏死和慢性炎症。最重要的特征是肉芽肿的存在与否以及促炎/抗炎细胞因子平衡的混合情况。当存在肉芽肿时,IFN-γ的表达显著更高,而在没有肉芽肿的溃疡病变中,IL-10的表达增加且细菌计数显著更高。这些特征与病变的慢性程度相关;持续时间较长的病变显示有肉芽肿。因此,相对早期的溃疡病变中没有肉芽肿,这些病变含有更多细菌且IFN-γ较少,这表明在疾病的这个阶段,保护性细胞免疫反应的强烈抑制促进了细菌的增殖。