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Association between IFNA genotype and the risk of systemic lupus erythematosus
Authors:Hitoshi Nakashima  Sawako Matsuno  Mitsuteru Akahoshi  Katsuhisa Miyake  Yasushi Inoue  Yosuke Tanaka  Ichiro Ninomiya  Sakiko Shimizu  Takashi Igawa  Atsushi Sadanaga  Takeshi Otsuka  Mine Harada
Affiliation:(1) Department of Medicine and Biosystemic Science, Graduate School of Medical Science, Kyushu University, Maidashi 3-1-1, 812-8582 Higashi-ku, Fukuoka, Japan;(2) Laboratory for Genetics of Allergic Diseases, SNP Research Center, RIKEN Yokohama Institute, The Institute of Physical and Chemical Research, Yokohama, Japan
Abstract:Systemic lupus erythematosus (SLE) is characterized by multisystem inflammation and production of autoantibodies, which can generate immune complexes and may cause tissue damage through the recognition of an autoantigen. Although many factors have been proposed, such as genetic factors, environmental factors, hormonal action, viruses, and dysregulation of cytokine production, the cause of this disease is not well understood. It has been reported that the levels of interferon (IFN)-agr in the sera of some SLE patients are elevated and that IFN-agr induces maturation of monocytes into highly active antigen-presenting dendritic cells (DCs). We analyzed the association between IFN-agr genotype and the risk of SLE to clarify whether IFN-agr plays a central role in susceptibility to SLE. The results showed that no IFN-agr genotype was significantly associated with the risk of SLE.
Keywords:IFN-  /content/jn1aek943cdvq7nw/xxlarge945.gif"   alt="  agr"   align="  BASELINE"   BORDER="  0"  >  IFNAI7 IFNAI0 polymorphism  Systemic lupus erythematosus (SLE)  Th1/Th2 balance
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