Regulatory macrophages: Setting the Threshold for Therapy

被引:159
作者
Fleming, Bryan D.
Mosser, David M. [1 ]
机构
[1] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
关键词
Immune regulation; Innate immunity; Inflammation; Macrophages; ALTERNATIVE ACTIVATION; RECEPTOR; CELLS; PHENOTYPE; POLARIZATION; EXPRESSION; TYPE-2;
D O I
10.1002/eji.201141717
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages exhibit remarkable plasticity and can change their phenotype in response to different environmental cues. They can become activated to kill intracellular microbes or they can assume regulatory properties to modulate immune responses. Regulatory macrophages are fundamentally different from classically activated, and we propose from nonclassically activated macrophages; they arise in response to different stimuli and perform different physiological functions. They are likely to express unique biochemical markers that could be exploited to identify and potentially target these macrophage subsets in tissue. Furthermore, inducers of regulatory macrophages may have the potential to be used as antiinflammatory therapeutics. Therefore, a better understanding of the various macrophage phenotypes may pave the way for new therapies that are directed at modulating macrophage functions or manipulating individual macrophage subsets.
引用
收藏
页码:2498 / 2502
页数:6
相关论文
共 26 条
[1]  
Anderson CF, 2002, J LEUKOCYTE BIOL, V72, P101
[2]   Biochemical and functional characterization of three activated macrophage populations [J].
Edwards, Justin P. ;
Zhang, Xia ;
Frauwirth, Kenneth A. ;
Mosser, David M. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 80 (06) :1298-1307
[3]   Immunological consequences of apoptotic cell phagocytosis [J].
Erwig, Lars-Peter ;
Henson, Peter M. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 171 (01) :2-8
[4]   Reversing lipopolysaccharide toxicity by ligating the macrophage Fcγ receptors [J].
Gerber, JS ;
Mosser, DM .
JOURNAL OF IMMUNOLOGY, 2001, 166 (11) :6861-6868
[5]   Alternative activation of macrophages [J].
Gordon, S .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (01) :23-35
[6]   Activation of a TGF-β-specific multistep gene expression program in mature macrophages requires glucocorticoid-mediated surface expression of TGF-β receptor II [J].
Gratchev, Alexei ;
Kzhyshkowska, Julia ;
Kannookadan, Sheila ;
Ochsenreiter, Miriam ;
Popova, Anna ;
Yu, Xiaolei ;
Mamidi, Srinivas ;
Stonehouse-Usselmann, Eugenia ;
Muller-Molinet, Isabelle ;
Gooi, LiMing ;
Goerdt, Sergij .
JOURNAL OF IMMUNOLOGY, 2008, 180 (10) :6553-6565
[7]   Gene Expression Profiling of Human Decidual Macrophages: Evidence for Immunosuppressive Phenotype [J].
Gustafsson, Charlotte ;
Mjoesberg, Jenny ;
Matussek, Andreas ;
Geffers, Robert ;
Matthiesen, Leif ;
Berg, Goeran ;
Sharma, Surendra ;
Buer, Jan ;
Ernerudh, Jan .
PLOS ONE, 2008, 3 (04)
[8]   ERK activation following macrophage FcγR ligation leads to chromatin modifications at the IL-10 locus [J].
Lucas, M ;
Zhang, X ;
Prasanna, V ;
Mosser, DM .
JOURNAL OF IMMUNOLOGY, 2005, 175 (01) :469-477
[9]   The chemokine system in diverse forms of macrophage activation and polarization [J].
Mantovani, A ;
Sica, A ;
Sozzani, S ;
Allavena, P ;
Vecchi, A ;
Locati, M .
TRENDS IN IMMUNOLOGY, 2004, 25 (12) :677-686
[10]   New vistas on macrophage differentiation and activation [J].
Mantovani, Alberto ;
Sica, Antonio ;
Locati, Massimo .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2007, 37 (01) :14-16