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1
Oral vaccination with Brucella melitensis WR201 protects mice against intranasal challenge with virulent Brucella melitensis 16M.用布鲁氏菌 melitensis WR201 进行口服疫苗接种可保护小鼠免受强毒布鲁氏菌 melitensis 16M 的鼻内攻击。
Infect Immun. 2004 Jul;72(7):4031-9. doi: 10.1128/IAI.72.7.4031-4039.2004.
2
Protection of mice against brucellosis by vaccination with Brucella melitensis WR201(16MDeltapurEK).用布鲁氏菌 melitensis WR201(16MDeltapurEK) 疫苗接种对小鼠进行布鲁氏菌病防护。
Infect Immun. 1999 Nov;67(11):5877-84. doi: 10.1128/IAI.67.11.5877-5884.1999.
3
Protection of BALB/c mice against homologous and heterologous species of Brucella by rough strain vaccines derived from Brucella melitensis and Brucella suis biovar 4.源自羊布鲁氏菌和猪布鲁氏菌生物变种4的粗糙型菌株疫苗对BALB/c小鼠抵抗同源和异源布鲁氏菌物种的保护作用。
Am J Vet Res. 1996 May;57(5):677-83.
4
Evaluation of Brucella melitensis B115 as rough-phenotype vaccine against B. melitensis and B. ovis infections.布鲁氏菌羊种B115作为抗羊种布鲁氏菌和绵羊布鲁氏菌感染的粗糙型表型疫苗的评估。
Vaccine. 2008 Sep 8;26(38):4913-7. doi: 10.1016/j.vaccine.2008.07.030. Epub 2008 Aug 15.
5
Enhanced efficacy of recombinant Brucella abortus RB51 vaccines against B. melitensis infection in mice.重组流产布鲁氏菌RB51疫苗对小鼠感染羊布鲁氏菌的增强疗效。
Vet Microbiol. 2004 Sep 8;102(3-4):237-45. doi: 10.1016/j.vetmic.2004.07.001.
6
A study on the use of male animal models for developing a live vaccine for brucellosis.一项关于使用雄性动物模型开发布鲁氏菌病活疫苗的研究。
Transbound Emerg Dis. 2008 May;55(3-4):145-51. doi: 10.1111/j.1865-1682.2008.01019.x.
7
Comparison of protective efficacy of subcutaneous versus intranasal immunization of mice with a Brucella melitensis lipopolysaccharide subunit vaccine.用羊布鲁氏菌脂多糖亚单位疫苗对小鼠进行皮下免疫与鼻内免疫的保护效果比较。
Infect Immun. 2006 Oct;74(10):5820-5. doi: 10.1128/IAI.00331-06.
8
Brucella melitensis 16MΔhfq attenuation confers protection against wild-type challenge in BALB/c mice.伯氏疏螺旋体 16MΔhfq 减毒株在 BALB/c 小鼠中可抵抗野生型菌株的攻击而产生保护作用。
Microbiol Immunol. 2013 Jul;57(7):502-10. doi: 10.1111/1348-0421.12065.
9
Protective live oral brucellosis vaccines stimulate Th1 and th17 cell responses.保护活疫苗口服布鲁氏菌病刺激 Th1 和 Th17 细胞反应。
Infect Immun. 2011 Oct;79(10):4165-74. doi: 10.1128/IAI.05080-11. Epub 2011 Jul 18.
10
Evaluation of the immunogenicity and the protective efficacy in mice of a DNA vaccine encoding SP41 from Brucella melitensis.对编码来自羊种布鲁氏菌SP41的DNA疫苗在小鼠中的免疫原性和保护效力的评估。
J Infect Dev Ctries. 2013 Apr 17;7(4):329-37. doi: 10.3855/jidc.2296.

引用本文的文献

1
Bactericidal Activity of Serum by RB51 Outer Membrane Protein's Combined by S99 Lipopolysaccharide Induction.RB51外膜蛋白与S99脂多糖诱导结合后血清的杀菌活性
Avicenna J Med Biotechnol. 2024 Jul-Sep;16(3):187-192. doi: 10.18502/ajmb.v16i3.15745.
2
A Single Nasal Dose Vaccination with a Brucella abortus Mutant Potently Protects against Pulmonary Infection.单次鼻腔接种布鲁氏菌突变体能有效预防肺部感染。
J Immunol. 2023 May 15;210(10):1576-1588. doi: 10.4049/jimmunol.2300071.
3
Activation of mucosal immunity as a novel therapeutic strategy for combating brucellosis.激活黏膜免疫作为对抗布鲁氏菌病的一种新型治疗策略。
Front Microbiol. 2022 Dec 22;13:1018165. doi: 10.3389/fmicb.2022.1018165. eCollection 2022.
4
Live mucosal vaccination stimulates potent protection varied CD4 and CD8 T cell subsets against wild-type 16M challenge.活黏膜疫苗接种刺激针对野生型 16M 挑战的多样化 CD4 和 CD8 T 细胞亚群产生强大的保护作用。
Front Immunol. 2022 Oct 3;13:995327. doi: 10.3389/fimmu.2022.995327. eCollection 2022.
5
Immune Response to Mucosal Infection.黏膜感染的免疫应答。
Front Immunol. 2019 Aug 20;10:1759. doi: 10.3389/fimmu.2019.01759. eCollection 2019.
6
Alternative strategies for vaccination to brucellosis.替代策略预防布鲁氏菌病疫苗接种。
Microbes Infect. 2018 Oct-Nov;20(9-10):599-605. doi: 10.1016/j.micinf.2017.12.006. Epub 2017 Dec 26.
7
Meta-Analysis and Advancement of Brucellosis Vaccinology.布鲁氏菌病疫苗学的Meta分析与进展
PLoS One. 2016 Nov 15;11(11):e0166582. doi: 10.1371/journal.pone.0166582. eCollection 2016.
8
The Case for Live Attenuated Vaccines against the Neglected Zoonotic Diseases Brucellosis and Bovine Tuberculosis.关于减毒活疫苗预防被忽视的人畜共患病布鲁氏菌病和牛结核病的理由
PLoS Negl Trop Dis. 2016 Aug 18;10(8):e0004572. doi: 10.1371/journal.pntd.0004572. eCollection 2016 Aug.
9
Protection efficacy of the Brucella abortus ghost vaccine candidate lysed by the N-terminal 24-amino acid fragment (GI24) of the 36-amino acid peptide PMAP-36 (porcine myeloid antimicrobial peptide 36) in murine models.在小鼠模型中,由36个氨基酸的肽PMAP - 36(猪髓样抗菌肽36)的N端24个氨基酸片段(GI24)裂解的布鲁氏菌流产株候选菌苗的保护效力。
J Vet Med Sci. 2016 Nov 1;78(10):1541-1548. doi: 10.1292/jvms.16-0036. Epub 2016 Jun 25.
10
Comparison between Immunization Routes of Live Attenuated Salmonella Typhimurium Strains Expressing BCSP31, Omp3b, and SOD of Brucella abortus in Murine Model.在小鼠模型中表达流产布鲁氏菌BCSP31、Omp3b和超氧化物歧化酶的减毒活鼠伤寒沙门氏菌菌株免疫途径的比较
Front Microbiol. 2016 Apr 20;7:550. doi: 10.3389/fmicb.2016.00550. eCollection 2016.

本文引用的文献

1
The use of live vaccine for vaccination of human beings against brucellosis in the USSR.苏联使用活疫苗对人类进行布鲁氏菌病疫苗接种。
Bull World Health Organ. 1961;24(1):85-9.
2
The fate of killed, radioiodinated Brucella abortus injected into mice.注入小鼠体内的经放射性碘化处理的灭活布鲁氏菌流产菌株的命运。
J Immunol. 1959 Apr;82(4):304-12.
3
Characterization of Brucella abortus O-polysaccharide and core lipopolysaccharide mutants and demonstration that a complete core is required for rough vaccines to be efficient against Brucella abortus and Brucella ovis in the mouse model.流产布鲁氏菌O-多糖和核心脂多糖突变体的特性分析以及在小鼠模型中证明粗糙型疫苗有效抵抗流产布鲁氏菌和绵羊布鲁氏菌需要完整的核心。
Infect Immun. 2003 Jun;71(6):3261-71. doi: 10.1128/IAI.71.6.3261-3271.2003.
4
Brucella abortus RB51 induces protection in mice orally infected with the virulent strain B. abortus 2308.布鲁氏菌RB51可诱导对口服强毒株布鲁氏菌2308感染的小鼠产生保护作用。
Infect Immun. 2003 May;71(5):2326-30. doi: 10.1128/IAI.71.5.2326-2330.2003.
5
Brucella species lacking the major outer membrane protein Omp25 are attenuated in mice and protect against Brucella melitensis and Brucella ovis.缺乏主要外膜蛋白Omp25的布鲁氏菌属菌株在小鼠体内毒力减弱,并能抵御羊种布鲁氏菌和绵羊布鲁氏菌。
Vet Microbiol. 2002 Sep 2;88(3):205-21. doi: 10.1016/s0378-1135(02)00110-4.
6
Comparison between immune responses and resistance induced in BALB/c mice vaccinated with RB51 and Rev. 1 vaccines and challenged with Brucella melitensis bv. 3.用RB51疫苗和Rev. 1疫苗接种BALB/c小鼠并以布鲁氏菌3型进行攻毒后诱导的免疫反应和抗性之间的比较。
Vet Microbiol. 2002 Aug 2;88(1):85-94. doi: 10.1016/s0378-1135(02)00088-3.
7
Protection of mice against brucellosis by intranasal immunization with Brucella melitensis lipopolysaccharide as a noncovalent complex with Neisseria meningitidis group B outer membrane protein.用布鲁氏菌脂多糖与B群脑膜炎奈瑟菌外膜蛋白形成的非共价复合物经鼻内免疫小鼠以预防布鲁氏菌病。
Infect Immun. 2002 Jul;70(7):3324-9. doi: 10.1128/IAI.70.7.3324-3329.2002.
8
Impaired control of Brucella melitensis infection in Rag1-deficient mice.Rag1基因缺陷小鼠对布鲁氏菌感染的控制受损。
Infect Immun. 2000 Sep;68(9):5314-20. doi: 10.1128/IAI.68.9.5314-5320.2000.
9
Overexpression of protective antigen as a novel approach to enhance vaccine efficacy of Brucella abortus strain RB51.保护性抗原的过表达作为一种增强流产布鲁氏菌RB51疫苗效力的新方法。
Infect Immun. 2000 Jun;68(6):3286-9. doi: 10.1128/IAI.68.6.3286-3289.2000.
10
Protection of mice against brucellosis by vaccination with Brucella melitensis WR201(16MDeltapurEK).用布鲁氏菌 melitensis WR201(16MDeltapurEK) 疫苗接种对小鼠进行布鲁氏菌病防护。
Infect Immun. 1999 Nov;67(11):5877-84. doi: 10.1128/IAI.67.11.5877-5884.1999.

用布鲁氏菌 melitensis WR201 进行口服疫苗接种可保护小鼠免受强毒布鲁氏菌 melitensis 16M 的鼻内攻击。

Oral vaccination with Brucella melitensis WR201 protects mice against intranasal challenge with virulent Brucella melitensis 16M.

作者信息

Izadjoo Mina J, Bhattacharjee Apurba K, Paranavitana Chrysanthi M, Hadfield Ted L, Hoover David L

机构信息

Department of Infectious and Parasitic Diseases, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.

出版信息

Infect Immun. 2004 Jul;72(7):4031-9. doi: 10.1128/IAI.72.7.4031-4039.2004.

DOI:10.1128/IAI.72.7.4031-4039.2004
PMID:15213148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC427460/
Abstract

Human brucellosis can be acquired from infected animal tissues by ingestion, inhalation, or contamination of conjunctiva or traumatized skin by infected animal products. In addition, Brucella is recognized as a biowarfare threat agent. Although a vaccine to protect humans from natural or deliberate infection could be useful, vaccines presently used in animals are unsuitable for human use. We tested orally administered live, attenuated, purine auxotrophic B. melitensis WR201 bacteria for their ability to elicit cellular and humoral immune responses and to protect mice against intranasal challenge with B. melitensis 16M bacteria. Immunized mice made serum antibody to lipopolysaccharide and non-O-polysaccharide antigens. Splenocytes from immunized animals released interleukin-2 and gamma interferon when grown in cultures with Brucella antigens. Immunization led to protection from disseminated infection and enhanced clearance of the challenge inoculum from the lungs. Optimal protection required administration of live bacteria, was related to immunizing dose, and was enhanced by booster immunization. These results establish the usefulness of oral vaccination against respiratory challenge with virulent Brucella and suggest that WR201 should be further investigated as a vaccine to prevent human brucellosis.

摘要

人类布鲁氏菌病可通过摄入、吸入感染动物组织,或感染动物产品污染结膜或创伤皮肤而获得。此外,布鲁氏菌被认为是一种生物战威胁剂。虽然一种能保护人类免受自然或蓄意感染的疫苗可能会有用,但目前用于动物的疫苗不适用于人类。我们测试了口服减毒活的嘌呤营养缺陷型羊种布鲁氏菌WR201细菌引发细胞免疫和体液免疫反应以及保护小鼠抵抗羊种布鲁氏菌16M细菌鼻内攻击的能力。免疫小鼠产生了针对脂多糖和非O-多糖抗原的血清抗体。免疫动物的脾细胞在与布鲁氏菌抗原一起培养时释放白细胞介素-2和γ干扰素。免疫可预防播散性感染,并增强从肺部清除攻击接种物的能力。最佳保护需要给予活细菌,与免疫剂量有关,并通过加强免疫得到增强。这些结果证实了口服疫苗预防强毒布鲁氏菌呼吸道攻击的有效性,并表明WR201作为预防人类布鲁氏菌病的疫苗应进一步研究。