Exosomes are an effective vaccine against congenital toxoplasmosis in mice

被引:90
作者
Beauvillain, Celine [1 ,2 ]
Juste, Matthieu O. [1 ,2 ]
Dion, Sarah [1 ,2 ]
Pierre, Josette [1 ,2 ]
Dimier-Poisson, Isabelle [1 ,2 ]
机构
[1] Univ INRA Immunol Parasitaire & Vaccinol, UMR 0483, IFR Agents Transmissibles & Infectiol, UFR Sci Pharmaceut, F-37200 Tours, France
[2] Univ Tours, INRA, F-37200 Tours, France
关键词
Congenital toxoplamosis; Exosomes; Vaccination; DENDRITIC CELL-LINE; IFN-GAMMA; IMMUNE-RESPONSE; GONDII INFECTION; T-CELLS; BIOGENESIS; RESISTANCE; IL-12; TNF; STIMULATION;
D O I
10.1016/j.vaccine.2009.01.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toxoplasmosis is a serious disease in humans and may cause abortion or congenital infection if a woman is exposed to the disease for the first time during pregnancy. Infection before pregnancy normally results in immunity protecting the foetus, suggesting that it may be possible to block vertical transmission of the parasite by appropriate vaccination before pregnancy. We found that the vaccination of CBA/J mice, before pregnancy, with exosomes secreted by SRDCs pulsed in vitro with Toxoplasma gondii-derived antigens (TAg) induced a protective response in the pups. Indeed, vaccination resulted in the presence of significantly fewer cysts in pup brains. This protection was associated with strong humoral responses in the serum in vivo. We also observed cellular responses in vivo, with cell proliferation associated with the production of cytokines by the splenocytes. Thus, exosomes are nucleic acid-free vesicles able to induce immune responses correlated with protection against T gondii infection in a congenital model. They are therefore a potentially useful tool for vaccination against infectious disease. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1750 / 1757
页数:8
相关论文
共 39 条
[1]   Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T gondii infection [J].
Aline, F ;
Bout, D ;
Amigorena, S ;
Roingeard, P ;
Dimier-Poisson, I .
INFECTION AND IMMUNITY, 2004, 72 (07) :4127-4137
[2]   Exosomes as potent cell-free peptide-based vaccine.: I.: Dendritic cell-derived exosomes transfer functional MHC class I/peptide complexes to dendritic cells [J].
André, F ;
Chaput, N ;
Schartz, NEC ;
Flament, C ;
Aubert, N ;
Bernard, J ;
Lemonnier, F ;
Raposo, G ;
Escudier, B ;
Hsu, DH ;
Tursz, T ;
Amigorena, S ;
Angevin, E ;
Zitvogel, L .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :2126-2136
[3]   A vaccine based on exosomes secreted by a dendritic cell line confers protection against T. gondii infection in syngeneic and allogeneic mice [J].
Beauvillain, Celine ;
Ruiz, Sophie ;
Guiton, Rachel ;
Bout, Daniel ;
Dimier-Poisson, Isabelle .
MICROBES AND INFECTION, 2007, 9 (14-15) :1614-1622
[4]   Preliminary estimates of the direct costs associated with endemic diseases of livestock in Great Britain [J].
Bennett, R ;
Christiansen, K ;
Clifton-Hadley, R .
PREVENTIVE VETERINARY MEDICINE, 1999, 39 (03) :155-171
[5]   Rapid recruitment of neutrophils containing prestored IL-12 during microbial infection [J].
Bliss, SK ;
Butcher, BA ;
Denkers, EY .
JOURNAL OF IMMUNOLOGY, 2000, 165 (08) :4515-4521
[6]  
CHARDES T, 1990, INFECT IMMUN, V58, P1240
[7]   T lymphocyte-dependent effector mechanisms of immunity to Toxoplasma gondii [J].
Denkers, EY .
MICROBES AND INFECTION, 1999, 1 (09) :699-708
[8]   Protective mucosal Th2 immune response against Toxoplasma gondii by murine mesenteric lymph node dendritic cells [J].
Dimier-Poisson, I ;
Aline, F ;
Mévélec, MN ;
Beauvillain, C ;
Buzoni-Gatel, D ;
Bout, D .
INFECTION AND IMMUNITY, 2003, 71 (09) :5254-5265
[9]   Mother-to-child transmission of toxoplasmosis: risk estimates for clinical counselling [J].
Dunn, D ;
Wallon, M ;
Peyron, F ;
Petersen, E ;
Peckham, C ;
Gilbert, R .
LANCET, 1999, 353 (9167) :1829-1833
[10]   Exosomes:: endosomal-derived vesicles shipping extracellular messages [J].
Février, B ;
Raposo, G .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (04) :415-421