Functions of granulocyte-macrophage colony-stimulating factor

被引:171
作者
Fleetwood, AJ
Cook, AD
Hamilton, JA [1 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Arthrit & Inflammat Res Ctr, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Cooperat Res Ctr Chron Inflammatory Dis, Parkville, Vic 3010, Australia
关键词
inflammation; macrophages; granulocytes; dendritic cells;
D O I
10.1615/CritRevImmunol.v25.i5.50
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
GM-CSF was originally defined by its ability to generate in vitro granulocyte and macrophage colonies from bone marrow precursor cells. Apart from its physiological role in the control of alveolar macrophage development, it now appears more likely that its major role lies in its ability to govern the properties of the more mature myeloid cells of the granulocyte and macrophage lineages, particularly during host defence and inflammatory reactions. Recent evidence is summarized below for a key role for GM-CSF in inflammatory and autoimmune diseases, making it therefore worthy of consideration for targeting. Such evidence includes disease exacerbation following its administration and amelioration of disease in animal models by GM-CSF gene targeting or by anti-GM-CSF antibody blockade. This review summarizes the evidence supporting a major role for GM-CSF in inflammation and autoimmunity and its functions as major regulator governing granulocyte and macrophage lineage populations at all stages of maturation.
引用
收藏
页码:405 / 428
页数:24
相关论文
共 264 条
[81]   MUTAGENESIS OF MURINE GRANULOCYTE MACROPHAGE-COLONY-STIMULATING FACTOR REVEALS CRITICAL RESIDUES NEAR THE N-TERMINUS [J].
GOUGH, NM ;
GRAIL, D ;
GEARING, DP ;
METCALF, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 169 (02) :353-358
[82]   PREVENTION OF EXPERIMENTAL CEREBRAL MALARIA BY ANTICYTOKINE ANTIBODIES - INTERLEUKIN-3 AND GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR ARE INTERMEDIATES IN INCREASED TUMOR NECROSIS FACTOR PRODUCTION AND MACROPHAGE ACCUMULATION [J].
GRAU, GE ;
KINDLER, V ;
PIGUET, PF ;
LAMBERT, PH ;
VASSALLI, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (04) :1499-1504
[83]   New role for Shc in activation of the phosphatidylinositol 3-kinase/Akt pathway [J].
Gu, HH ;
Maeda, H ;
Moon, JJ ;
Lord, JD ;
Yoakim, M ;
Nelson, BH ;
Neel, BG .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (19) :7109-7120
[84]  
GUALTIERI RJ, 1989, BLOOD, V74, P2360
[85]   Mechanism of activation of the GM-CSF IL-3, and IL-5 family of receptors [J].
Guthridge, MA ;
Stomski, FC ;
Thomas, D ;
Woodcock, JM ;
Bagley, CJ ;
Berndt, MC ;
Lopez, AF .
STEM CELLS, 1998, 16 (05) :301-313
[86]   Site-specific serine phosphorylation of the IL-3 receptor is required for hemopoietic cell survival [J].
Guthridge, MA ;
Stomski, FC ;
Barry, EF ;
Winnall, W ;
Woodcock, JM ;
McClure, BJ ;
Dottore, M ;
Berndt, MC ;
Lopez, AF .
MOLECULAR CELL, 2000, 6 (01) :99-108
[87]   The phosphoserine-585-dependent pathway of the GM-CSF/IL-3/IL-5 receptors mediates hematopoietic cell survival through activation of NF-κB and induction of bcl-2 [J].
Guthridge, MA ;
Barry, EF ;
Felquer, FA ;
McClure, BJ ;
Stomski, FC ;
Ramshaw, H ;
Lopez, AF .
BLOOD, 2004, 103 (03) :820-827
[88]   Role of granulocyte-macrophage colony-stimulating factor in preventing apoptosis and improving functional outcome in experimental spinal cord contusion injury [J].
Ha, Y ;
Kim, YS ;
Cho, JM ;
Yoon, SH ;
Park, SR ;
Yoon, DH ;
Kim, EY ;
Park, HC .
JOURNAL OF NEUROSURGERY-SPINE, 2005, 2 (01) :55-61
[89]   Antibody response to DT-GM, a novel fusion toxin consisting of a truncated diphtheria toxin (DT) linked to human granulocyte-macrophage colony stimulating factor (GM), during a phase I trial of patients with relapsed or refractory acute myeloid leukemia [J].
Hall, PD ;
Virella, G ;
Willoughby, T ;
Atchley, DH ;
Kreitman, RJ ;
Frankel, AE .
CLINICAL IMMUNOLOGY, 2001, 100 (02) :191-197
[90]   DT388-GM-CSF, a novel fusion toxin consisting of a truncated diphtheria toxin fused to human granulocyte-macrophage colony-stimulating factor, prolongs host survival in a SCID mouse model of acute myeloid leukemia [J].
Hall, PD ;
Willingham, MC ;
Kreitman, RJ ;
Frankel, AE .
LEUKEMIA, 1999, 13 (04) :629-633