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本文引用的文献

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Pathophysiology of toxoplasmosis.弓形虫病的病理生理学
Parasitol Today. 1988 Oct;4(10):273-8. doi: 10.1016/0169-4758(88)90018-x.
2
CD8(+)-T-cell immunity against Toxoplasma gondii can be induced but not maintained in mice lacking conventional CD4(+) T cells.在缺乏传统CD4(+) T细胞的小鼠中,可以诱导出针对刚地弓形虫的CD8(+) T细胞免疫,但无法维持这种免疫。
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Deficient humoral responses underlie susceptibility to Toxoplasma gondii in CD4-deficient mice.体液免疫反应缺陷是CD4缺陷小鼠对刚地弓形虫易感的基础。
Infect Immun. 2002 Jan;70(1):185-91. doi: 10.1128/IAI.70.1.185-191.2002.
4
Monocyte-derived CD1a+ and CD1a- dendritic cell subsets differ in their cytokine production profiles, susceptibilities to transfection, and capacities to direct Th cell differentiation.单核细胞衍生的CD1a+和CD1a-树突状细胞亚群在细胞因子产生谱、转染易感性以及指导Th细胞分化的能力方面存在差异。
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Cutting edge: IL-12 is required for the maintenance of IFN-gamma production in T cells mediating chronic resistance to the intracellular pathogen, Toxoplasma gondii.前沿:白细胞介素-12是介导对细胞内病原体弓形虫慢性抗性的T细胞中维持γ-干扰素产生所必需的。
J Immunol. 2000 Jul 15;165(2):628-31. doi: 10.4049/jimmunol.165.2.628.
6
CCR6 mediates dendritic cell localization, lymphocyte homeostasis, and immune responses in mucosal tissue.CCR6介导树突状细胞在黏膜组织中的定位、淋巴细胞稳态及免疫反应。
Immunity. 2000 May;12(5):495-503. doi: 10.1016/s1074-7613(00)80201-0.
7
Decreased resistance of B cell-deficient mice to infection with Toxoplasma gondii despite unimpaired expression of IFN-gamma, TNF-alpha, and inducible nitric oxide synthase.B细胞缺陷小鼠对刚地弓形虫感染的抵抗力降低,尽管其γ干扰素、肿瘤坏死因子-α和诱导型一氧化氮合酶的表达未受影响。
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B cells are essential for vaccination-induced resistance to virulent Toxoplasma gondii.B细胞对于疫苗接种诱导的对强毒力刚地弓形虫的抵抗力至关重要。
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9
Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells.新鲜分离的派尔集合淋巴结而非脾脏的树突状细胞可产生白细胞介素10,并诱导2型辅助性T细胞分化。
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10
Definition of dendritic cell subpopulations present in the spleen, Peyer's patches, lymph nodes, and skin of the mouse.小鼠脾脏、派尔集合淋巴结、淋巴结和皮肤中存在的树突状细胞亚群的定义。
Blood. 1999 Jan 15;93(2):590-8.

小鼠肠系膜淋巴结树突状细胞对刚地弓形虫的保护性黏膜Th2免疫反应

Protective mucosal Th2 immune response against Toxoplasma gondii by murine mesenteric lymph node dendritic cells.

作者信息

Dimier-Poisson Isabelle, Aline Fleur, Mévélec Marie-Noëlle, Beauvillain Céline, Buzoni-Gatel Dominique, Bout Daniel

机构信息

UMR Université-INRA d'Immunologie Parasitaire et Vaccinologia, UFR des Sciences Pharmaceutiques, 37200 Tours, France.

出版信息

Infect Immun. 2003 Sep;71(9):5254-65. doi: 10.1128/IAI.71.9.5254-5265.2003.

DOI:10.1128/IAI.71.9.5254-5265.2003
PMID:12933872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC187296/
Abstract

Toxoplasma gondii, an obligate intracellular parasite pathogen which initially invades the intestinal epithelium before disseminating throughout the body, may cause severe sequelae in fetuses and life-threatening neuropathy in immunocompromised patients. Immune protection is usually thought to be performed through a systemic Th1 response; considering the route of parasite entry it is important to study and characterize the local mucosal immune response to T. gondii. Despite considerable effort, Toxoplasma-targeted vaccines have proven to be elusive using conventional strategies. We report the use of mesenteric lymph node dendritic cells (MLNDCs) pulsed ex vivo with T. gondii antigens (TAg) as a novel investigation approach to vaccination against T. gondii-driven pathogenic processes. Using a murine model, we demonstrate in two genetically distinct mouse strains (C57BL/6 and CBA/J) that adoptively transferred TAg-pulsed MLNDCs elicit a mucosal Toxoplasma-specific Th2-biased immune response in vivo and confer strong protection against infection. We also observe that MLNDCs mostly traffic to the intestine where they enhance resistance by reduction in the mortality and in the number of brain cysts. Thus, ex vivo TAg-pulsed MLNDCs represent a powerful tool for the study of protective immunity to T. gondii, delivered through its natural route of entry. These findings might impact the design of vaccine strategies against other invasive microorganisms known to be delivered through digestive tract.

摘要

刚地弓形虫是一种专性细胞内寄生性病原体,最初侵入肠道上皮,然后扩散至全身,可导致胎儿出现严重后遗症,并在免疫功能低下的患者中引发危及生命的神经病变。通常认为免疫保护是通过全身性Th1反应来实现的;考虑到寄生虫的侵入途径,研究和表征针对刚地弓形虫的局部黏膜免疫反应非常重要。尽管付出了巨大努力,但事实证明,使用传统策略难以研制出针对弓形虫的疫苗。我们报告了一种新的疫苗接种研究方法,即使用在体外经刚地弓形虫抗原(TAg)脉冲处理的肠系膜淋巴结树突状细胞(MLNDCs)来对抗刚地弓形虫引发的致病过程。利用小鼠模型,我们在两种基因不同的小鼠品系(C57BL/6和CBA/J)中证明,过继转移经TAg脉冲处理的MLNDCs可在体内引发黏膜针对弓形虫的、以Th2为主的免疫反应,并提供强大的抗感染保护。我们还观察到,MLNDCs大多迁移至肠道,通过降低死亡率和减少脑囊肿数量来增强抵抗力。因此,体外经TAg脉冲处理的MLNDCs是研究通过刚地弓形虫自然侵入途径产生的针对其保护性免疫的有力工具。这些发现可能会影响针对已知通过消化道传播的其他侵袭性微生物的疫苗策略设计。