A vaccine based on exosomes secreted by a dendritic cell line confers protection against T. gondii infection in syngeneic and allogeneic mice

被引:105
作者
Beauvillain, Celine [1 ,2 ,3 ]
Ruiz, Sophie [2 ]
Guiton, Rachel [2 ]
Bout, Daniel [2 ]
Dimier-Poisson, Isabelle [2 ]
机构
[1] Univ Hosp, Unite Mixte Inst Natl St & Rech Med 564, 4 Rue Larrey, F-49933 Angers, France
[2] Univ Tours, Univ INRA Immunol Parasitaire & Vaccinol, IFR Agents Transmissibles & Infectiol, UFR Sci Pharmaceut,UMR 0483,INRA, F-37200 Tours, France
[3] Univ Hosp, Immunol & Allergol Lab, Angers, France
关键词
exosomes; dendritic cells; Toxoplasma gondii; vaccine;
D O I
10.1016/j.micinf.2007.07.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Our results show that exosomes secreted by SRDC pulsed in vitro with Toxoplasma gondii-derived antigens (Exo-TAg) induced protective responses against infection with the parasite in both syngeneic and allogeneic mice. After oral infection, syngeneic CBA/J mice exhibited significantly fewer cysts in their brains and allogeneic C57BL/6 mice survived. This protection was associated with strong humoral responses in vivo in serum from both CBA/J and C57BL/6 mice, and with high levels of anti-TAg IgA antibodies in intestinal secretions from CBA/J mice alone. Furthermore, strong cellular responses in vivo were observed in both mouse models. Cellular proliferation was associated with cytokines production by spleen and mesenteric lymph node cells. The results presented here show that exosomes are nucleic acid free vesicles that are able to induce immune responses correlated with protection against parasitic infections in both syngeneic and allogeneic mice. They could constitute an efficient tool for use in vaccination and antitumor strategies based on exosomes. (c) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1614 / 1622
页数:9
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