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Enhanced Susceptibility to Leishmania Infection in Resistant Mice in the Absence of Immediate Early Response Gene X-1
被引:20
作者:
Akilov, Oleg E.
[1
]
Ustyugova, Irina V.
[1
]
Zhi, Liang
[1
]
Hasan, Tayyaba
[1
]
Wu, Mei X.
[1
]
机构:
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Wellman Ctr Photomed,Dept Dermatol, Boston, MA 02114 USA
基金:
美国国家卫生研究院;
关键词:
REGULATORY T-CELLS;
CUTANEOUS LEISHMANIASIS;
MAJOR INFECTION;
NITRIC-OXIDE;
BALB/C MICE;
ACTIVATED MACROPHAGES;
NATURAL MODEL;
IFN-GAMMA;
KAPPA-B;
INDUCTION;
D O I:
10.4049/jimmunol.0900866
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Immediate early response gene X-1 (IEX-1) is a stress-inducible gene abundantly expressed in macrophages and T cells following various stimuli. To explore a potential role for IEX-1 in control of the susceptibility to Leishmania major infection, the inflammatory response during cutaneous leishmaniasis was evaluated in 129Sv/C57BL/6-resistant mice in the presence or absence of IEX-1. Null mutation of IEX-1 enhanced the susceptibility of the mice to L. major infection, and aggravated inflammatory responses in comparison with wild-type control mice. The excessive inflammation was not ascribed to a Th2-biased immune response or a defect in Th1 polarization, but rather to an elevated level of IL-17 production by both gamma delta T and CD4(+) cells, concomitant with an increase of the neutrophil recruitment early in the infection. The lack of IEX-1 also suppressed TNF-alpha production in both macrophages and T cells, resulting in a high intralesional load, of parasites-and delayed healing of the lesion, both of which were reversed by TNF-alpha treatment. These findings indicate the crucial role of IL-17 and TNF-alpha in determining the outcome of L. major infection beyond a balance between Th1- and Th2-mediated immune responses. The Journal of Immunology, 2009, 183: 7994-8003.
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页码:7994 / 8003
页数:10
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