The critical role of mast cells in allergy and inflammation

被引:227
作者
Theoharides, Theoharis C.
Kalogeromitros, Dimitrios
机构
[1] Tufts Univ, Sch Med, Dept Pharmacol & Expt Therapeut, Tufts New England Med Ctr, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Dept Biochem, Tufts New England Med Ctr, Boston, MA 02111 USA
[3] Tufts Univ, Sch Med, Dept Internal Med, Tufts New England Med Ctr, Boston, MA 02111 USA
[4] Univ Athens, Sch Med, Attikon Hosp, Div Allergy, GR-10679 Athens, Greece
来源
NEUROENDOCRINE AND IMMUNE CROSSTALK | 2006年 / 1088卷
关键词
asthma; coronary artery disease; inflammation; dermatoses; mast cells; skin; stress; vascular permeability;
D O I
10.1196/annals.1366.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mast cells are well known for their involvement in allergic and anaphylactic reactions, but recent findings implicate them in a variety of inflammatory diseases affecting different organs, including the heart, joints, lungs, and skin. In these cases, mast cells appear to be activated by triggers other than aggregation of their IgE receptors (Fc epsilon RI), such as anaphylatoxins, immunoglobulin-free light chains, superantigens, neuropeptides, and cytokines leading to selective release of mediators without degranulation. These findings could explain inflammatory diseases, such as asthma, atopic dermatitis, coronary inflammation, and inflammatory arthritis, all of which worsen by stress. It is proposed that the pathogenesis of these diseases involve mast cell activation by local release of corticotropin-releasing hormone (CRH) or related peptides. Combination of CRH receptor antagonists and mast cell inhibitors may present novel therapeutic interventions.
引用
收藏
页码:78 / 99
页数:22
相关论文
共 208 条
[41]  
DEANFIELD JE, 1984, LANCET, V2, P1001
[42]   MENTAL STRESS, PAIN PERCEPTION AND RISK OF SILENT ISCHEMIA [J].
DEEDWANIA, PC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1995, 25 (07) :1504-1506
[43]   Sites of interleukin-16 release in patients with acute coronary syndromes and in patients with congestive heart failure [J].
Deliargyris, EN ;
Raymond, RJ ;
Theoharides, TC ;
Boucher, WS ;
Tate, DA ;
Dehmer, GJ .
AMERICAN JOURNAL OF CARDIOLOGY, 2000, 86 (09) :913-918
[44]   MULTIPLE REGULATORY ELEMENTS IN THE INTERLEUKIN-6 GENE MEDIATE INDUCTION BY PROSTAGLANDINS, CYCLIC-AMP, AND LIPOPOLYSACCHARIDE [J].
DENDORFER, U ;
OETTGEN, P ;
LIBERMANN, TA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) :4443-4454
[45]   Human synovial mast cells .1. Ultrastructural in situ and in vitro immunologic characterization [J].
dePaulis, A ;
Marino, I ;
Ciccarelli, A ;
deCrescenzo, G ;
Concardi, M ;
Verga, L ;
Arbustini, E ;
Marone, G .
ARTHRITIS AND RHEUMATISM, 1996, 39 (07) :1222-1233
[46]   Human synovial mast cells .2. Heterogeneity of the pharmacologic effects of antiinflammatory and immunosuppressive drugs [J].
dePaulis, A ;
Ciccarelli, A ;
Marino, I ;
deCrescenzo, G ;
Marino, D ;
Marone, G .
ARTHRITIS AND RHEUMATISM, 1997, 40 (03) :469-478
[47]   Enhancing versus suppressive effects of stress hormones on skin immune function [J].
Dhabhar, FS ;
McEwen, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :1059-1064
[48]  
Dhabhar FS, 1996, J IMMUNOL, V156, P2608
[49]  
DIMITRIADOU V, 1991, NEUROSCIENCE, V44, P97
[50]   HISTOCHEMICAL AND ULTRASTRUCTURAL CHARACTERISTICS OF RAT-BRAIN PERIVASCULAR MAST-CELLS STIMULATED WITH COMPOUND 48/80 AND CARBACHOL [J].
DIMITRIADOU, V ;
LAMBRACHTHALL, M ;
REICHLER, J ;
THEOHARIDES, TC .
NEUROSCIENCE, 1990, 39 (01) :209-224