The macrophages in rheumatic diseases

被引:121
作者
Laria, Antonella [1 ]
Lurati, Alfredomaria [1 ]
Marrazza, Mariagrazia [1 ]
Mazzocchi, Daniela [1 ]
Re, Katia Angela [1 ]
Scarpellini, Magda [1 ]
机构
[1] Fornaroli Hosp, Rheumatol Unit, Via Donatore Sangue 50, I-20013 Magenta, MI, Italy
关键词
macrophage; rheumatic diseases;
D O I
10.2147/JIR.S82320
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Macrophages belong to the innate immune system giving us protection against pathogens. However it is known that they are also involved in rheumatic diseases. Activated macrophages have two different phenotypes related to different stimuli: M1 (classically activated) and M2 (alternatively activated). M1 macrophages release high levels of pro-inflammatory cytokines, reactive nitrogen and oxygen intermediates killing microorganisms and tumor cells; while M2 macrophages are involved in resolution of inflammation through phagocytosis of apoptotic neutrophils, reduced production of pro-inflammatory cytokines, and increased synthesis of mediators important in tissue remodeling, angiogenesis, and wound repair. The role of macrophages in the different rheumatic diseases is different according to their M1/M2 macrophages phenotype.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 92 条
[1]
Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[2]
Serum of patients with Behcet's disease induces classical (pro-inflammatory) activation of human macrophages in vitro [J].
Alpsoy, E ;
Kodelja, V ;
Goerdt, S ;
Orfanos, CE ;
Zouboulis, CC .
DERMATOLOGY, 2003, 206 (03) :225-232
[3]
Systematic validation of specific phenotypic markers for in vitro polarized human macrophages [J].
Ambarus, C. A. ;
Krausz, S. ;
van Eijk, M. ;
Hamann, J. ;
Radstake, T. R. D. J. ;
Reedquist, K. A. ;
Tak, P. P. ;
Baeten, D. L. P. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2012, 375 (1-2) :196-206
[4]
Imatinib mesylate inhibits osteoclastogenesis and joint destruction in rats with collagen-induced arthritis (CIA) [J].
Ando, Wataru ;
Hashimoto, Jun ;
Nampei, Akihide ;
Tsuboi, Hideki ;
Tateishi, Kosuke ;
Ono, Takeshi ;
Nakamura, Norimasa ;
Ochi, Takahiro ;
Yoshikawa, Hideki .
JOURNAL OF BONE AND MINERAL METABOLISM, 2006, 24 (04) :274-282
[5]
Reciprocal relation between GADD153 and Del-1 in regulation of salivary gland inflammation in Sjogren syndrome [J].
Baban, Babak ;
Liu, Jun Yao ;
Abdelsayed, Rafik ;
Mozaffari, Mahmood S. .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2013, 95 (03) :288-297
[6]
Immune response to biologic scaffold materials [J].
Badylak, Stephen E. ;
Gilbert, Thomas W. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :109-116
[7]
Macrophages expressing the scavenger receptor CD163: a link between immune alterations of the gut and synovial inflammation in spondyloarthropathy [J].
Baeten, D ;
Demetter, P ;
Cuvelier, CA ;
Kruithof, E ;
Van Damme, N ;
De Vos, M ;
Veys, EM ;
De Keyser, F .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :343-350
[8]
Diagnostic classification of spondylarthropathy and rheumatoid arthritis by synovial histopathology - A prospective study in 154 consecutive patients [J].
Baeten, D ;
Kruithof, E ;
De Rycke, L ;
Vandooren, B ;
Wyns, B ;
Boullart, L ;
Hoffman, IEA ;
Boots, AM ;
Veys, EM ;
De Keyser, F .
ARTHRITIS AND RHEUMATISM, 2004, 50 (09) :2931-2941
[9]
Smoldering and polarized inflammation in the initiation and promotion of malignant disease [J].
Balkwill, F ;
Charles, KA ;
Mantovani, A .
CANCER CELL, 2005, 7 (03) :211-217
[10]
Type I interferon in systemic lupus erythematosus and other autoimmune diseases [J].
Banchereau, Jacques ;
Pascual, Virginia .
IMMUNITY, 2006, 25 (03) :383-392