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.
引用
收藏
页码:7994 / 8003
页数:10
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