Dimier-Poisson Isabelle, Aline Fleur, Mévélec Marie-Noëlle, Beauvillain Céline, Buzoni-Gatel Dominique, Bout Daniel
UMR Université-INRA d'Immunologie Parasitaire et Vaccinologia, UFR des Sciences Pharmaceutiques, 37200 Tours, France.
Infect Immun. 2003 Sep;71(9):5254-65. doi: 10.1128/IAI.71.9.5254-5265.2003.
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.
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。