Chemokines and common variable immunodeficiency; possible contribution of the fractalkine system (CX3CL1/CX3CR1) to chronic inflammation

被引:11
作者
Fevang, Borre [1 ]
Yndestad, Arne [1 ]
Damas, Jan K. [1 ,2 ]
Bjerkeli, Vigdis [1 ]
Ueland, Thor [1 ,3 ]
Holm, Are M. [1 ,4 ]
Beiske, Klaus [1 ,5 ]
Aukrust, Pal [1 ,2 ]
Froland, Stig S. [1 ,2 ]
机构
[1] Univ Oslo, Rikshosp, Internal Med Res Inst, N-0027 Oslo, Norway
[2] Univ Oslo, Rikshosp, Sect Clin Immunol & Infect Dis, N-0027 Oslo, Norway
[3] Univ Oslo, Rikshosp, Endocrinol Sect, N-0027 Oslo, Norway
[4] Univ Oslo, Rikshosp, Dept Resp Med, N-0027 Oslo, Norway
[5] Univ Oslo, Rikshosp, Dept Pathol, N-0027 Oslo, Norway
关键词
CVID; Chronic inflammation; Chemokines; Fractalkine; CX3CL1; CX3CR1; Splenomegaly; T-CELLS; INCREASED EXPRESSION; SOLUBLE FRACTALKINE; INTERFERON-GAMMA; GENE-EXPRESSION; DENDRITIC CELLS; CX3C CHEMOKINE; SERUM-LEVELS; LOW NUMBERS; RECEPTOR;
D O I
10.1016/j.clim.2008.09.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Common variable immunodeficiency (CVID) is a heterogeneous syndrome characterized by defective immunoglobulin production and high frequency of bacterial infections, autoimmunity and manifestations of chronic inflammation. The chemokine Fractalkine (CX3CL1) and its receptor CX3CR1 is suggested to play an important rote in the pathogenesis of several inflammatory disorders. We hypothesized that enhanced CX3CL1/CX3CR1 interaction could be involved in the chronic inflammation characterising subgroups of CVID. CVID patients were characterized by raised plasma levels of CX3CL1 and enhanced expression of its corresponding receptor CX3CR1 on CD4(+) and CD8(+) T cells, including both CD45RA(+) and CD45RA(-) subsets. CX3CR1 expression was particularly enhanced in patients characterized by chronic inflammation in vivo. The high expression of the receptor in CVID patients was accompanied by enhanced chemotactic, adhesive, and other inflammatory cell responses to stimulation with CX3CL1. Our findings suggest that increased CX3CL1/CX3CR1 interaction could contribute to the inflammatory phenotype seen in subgroups of CVID patients. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:151 / 161
页数:11
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