CCR5 in T cell-mediated liver diseases: What's going on?

被引:50
作者
Ajuebor, Maureen N. [1 ]
Carey, Jillian A. [1 ]
Swain, Mark G. [1 ]
机构
[1] Univ Calgary, Fac Med, Gastrointestinal Res Grp, Calgary, AB T2N 4N1, Canada
关键词
D O I
10.4049/jimmunol.177.4.2039
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The chemokine receptor CCR5 came into worldwide prominence a decade ago when it was identified as one of the major coreceptors for HIV infectivity. However, subsequent studies suggested an important modulatory role for CCR5 in the inflammatory response. Specifically, CCR5 has been reported to directly regulate T cell function in autoimmune diseases, including multiple sclerosis, rheumatoid arthritis, and type 1 diabetes. Moreover, T cell-mediated immune responses are proposed to be critical in the pathogenesis of autoimmune and viral liver diseases, and recent clinical and experimental studies have also implicated CCR5 in the pathogenesis of autoimmune and viral liver diseases. Therefore, in this brief review, we highlight the evidence that supports an important role of CCR5 in the pathophysiology of T cell-mediated liver diseases with specific emphasis on autoimmune and viral liver diseases.
引用
收藏
页码:2039 / 2045
页数:7
相关论文
共 64 条
[1]  
Ajuebor M, 2005, HEPATOLOGY, V42, p250A
[2]   Role of chemokines and chemokine receptors in the gastrointestinal tract [J].
Ajuebor, MN ;
Swain, MG .
IMMUNOLOGY, 2002, 105 (02) :137-143
[3]   Lack of chemokine receptor CCR5 promotes murine fulminant liver failure by preventing the apoptosis of activated CD1d-restricted NKT cells [J].
Ajuebor, MN ;
Aspinall, AI ;
Zhou, F ;
Le, T ;
Yang, Y ;
Urbanski, SJ ;
Sidobre, W ;
Kronenberg, M ;
Hogaboam, CM ;
Swain, MG .
JOURNAL OF IMMUNOLOGY, 2005, 174 (12) :8027-8037
[4]   C-C chemokine ligand 2/monocyte chemoattractant protein-1 directly inhibits NKT cell IL-4 production and is hepatoprotective in T cell-mediated hepatitis in the mouse [J].
Ajuebor, MN ;
Hogaboam, CM ;
Le, T ;
Swain, MG .
JOURNAL OF IMMUNOLOGY, 2003, 170 (10) :5252-5259
[5]   CCL3/MIP-1α is pro-inflammatory in murine T cell-mediated hepatitis by recruiting CCR1-expressing CD4+ T cells to the liver [J].
Ajuebor, MN ;
Hogaboam, CM ;
Le, T ;
Proudfoot, AEI ;
Swain, MG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (10) :2907-2918
[6]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[7]   The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes [J].
Balabanian, K ;
Lagane, B ;
Infantino, S ;
Chow, KYC ;
Harriague, J ;
Moepps, B ;
Arenzana-Seisdedos, F ;
Thelen, M ;
Bachelerie, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (42) :35760-35766
[8]   DNA microarray analysis of chimpanzee liver during acute resolving hepatitis C virus infection [J].
Bigger, CB ;
Brasky, KM ;
Lanford, RE .
JOURNAL OF VIROLOGY, 2001, 75 (15) :7059-7066
[9]   Liver-infiltrating lymphocytes in end-stage hepatitis C virus: Subsets, activation status, and chemokine receptor phenotypes [J].
Boisvert, J ;
Kunkel, EJ ;
Campbell, JJ ;
Keeffe, EB ;
Butcher, EC ;
Greenberg, HB .
JOURNAL OF HEPATOLOGY, 2003, 38 (01) :67-75
[10]   Abnormal immune response of CCR5-deficient mice to ocular infection with herpes simplex virus type 1 [J].
Carr, DJJ ;
Ash, J ;
Lane, TE ;
Kuziel, WA .
JOURNAL OF GENERAL VIROLOGY, 2006, 87 :489-499