Title of article :
Chemokines and common variable immunodeficiency; possible contribution of the fractalkine system (CX3CL1/CX3CR1) to chronic inflammation
Author/Authors :
Fevang، نويسنده , , Bّrre and Yndestad، نويسنده , , Arne and Damهs، نويسنده , , Jan K. and Bjerkeli، نويسنده , , Vigdis and Ueland، نويسنده , , Thor and Holm، نويسنده , , Geir E. and Beiske، نويسنده , , Klaus and Aukrust، نويسنده , , Pهl and Frّland، نويسنده , , Stig S.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
11
From page :
151
To page :
161
Abstract :
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 role 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 CX3CLl 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.
Keywords :
Fractalkine , chronic inflammation , chemokines , Splenomegaly , CX3CL1 , CVID , CX3CR1
Journal title :
Clinical Immunology
Serial Year :
2009
Journal title :
Clinical Immunology
Record number :
1853761
Link To Document :
بازگشت