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A deficiency in the B cell response of C57BL/6 mice correlates with loss of macrophage-mediated killing of Leishmania amazonensis
被引:14
作者:
Gibson-Corley, Katherine N.
[1
]
Boggiatto, Paola M.
[1
]
Mukbel, Rami M.
[1
]
Petersen, Christine A.
[1
]
Jones, Douglas E.
[1
]
机构:
[1] Iowa State Univ, Dept Vet Pathol, Coll Vet Med, Ames, IA 50011 USA
基金:
美国国家卫生研究院;
关键词:
Cutaneous leishmaniasis;
Murine model;
Co-infection;
B cells;
Macrophages;
FC-RECEPTOR;
INFECTION;
SUSCEPTIBILITY;
AMASTIGOTES;
ANTIBODIES;
D O I:
10.1016/j.ijpara.2009.11.010
中图分类号:
R38 [医学寄生虫学];
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
100103 ;
摘要:
Infection of C3HeB/FeJ and C57BL/6 mice with Leishmania major stimulates a healing cell-mediated immune response, while Leishmania amazonensis infection leads to chronic disease. Here we show C3HeB/FeJ mice co-infected with both species of Leishmania heal, while co-infected C57BL/6 mice do not. Using an in vitro killing assay we determined B cells from infected C57BL/6 mice are ineffective in promoting parasite killing compared with B cells from infected C3HeB/FeJ mice. Furthermore, infected C57BL/6 mice produce less antigen-specific antibodies compared with infected C3HeB/FeJ mice. These findings Suggest B cells play a required role in the cell-mediated immune response against L. amazonensis. (C) 2009 Australian Society for Parasitology Inc. All rights reserved.
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页码:157 / 161
页数:5
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