Glucocorticoids and inflammation revisited: The state of the art

被引:93
作者
Franchimont, D [1 ]
Kino, T
Galon, J
Meduri, GU
Chrousos, G
机构
[1] NICHHD, Pediat & Reprod Endocrinol Branch, NIH, Bethesda, MD 20892 USA
[2] Erasme Univ Hosp, Gastroenterol Internal Med Dept, B-1070 Brussels, Belgium
[3] Inst Curie, INSERM 255, Paris, France
[4] Univ Tennessee, Ctr Hlth Sci, Div Pulm Med, Dept Med,Memphis Lung Res Progam, Memphis, TN 38163 USA
[5] Univ Tennessee, Ctr Hlth Sci, Div Crit Care Med, Dept Med,Memphis Lung Res Progam, Memphis, TN 38163 USA
关键词
glucocorticoids; cortisol; inflammation; HPA axis; DNA microarray; glucocorticoid resistance;
D O I
10.1159/000069969
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucocorticoids have been used in the treatment of inflammatory and autoimmune diseases and to prevent graft rejection for over 50 years. These hormones exert their effects through cytoplasmic, heat shock protein-bound glucocorticoid receptors that translocate into the nucleus, where they regulate the transcriptional activity of responsive genes by binding to specific promoter DNA sequences (transactivation) or by interacting with transcription factors (transrepression). By interacting with different signaling pathways, newly characterized nuclear receptor coregulators enhance or diminish the actions of glucocorticoids, thus explaining the gene-, cell-, tissue- and context-dependent actions of glucocorticoids. Glucocorticoids modulate genes involved in the priming of the innate immune response, while their actions on the adaptive immune response are to suppress cellular [T helper (Th)1-directed] immunity and promote humoral (Th2-directed) immunity and tolerance. The past decade has produced new insights into the mechanisms of glucocorticoid sensitivity and resistance of inflammatory, autoimmune and allergic diseases. Both the quality and severity of the inflammatory stimulus, as well as the genetics and constitution of the patient, play key roles in the glucocorticoid sensitivity, dependency and resistance of these diseases. Although glucocorticoids increase susceptibility to opportunistic infections, they are also highly beneficial in the presence of serious systemic inflammation, such as that observed in septic shock and acute respiratory distress syndrome, when administered in a sustained fashion throughout the course of the disease. Glucocorticoids produce their cardiovascular, metabolic and antigrowth side effects through molecular mechanisms distinct from those involved in immunomodulation. Fortunately, the first generation of tissue- and immune- versus cardiovascular/ metabolic effect-selective glucocorticoids is available for study and further improvement. 'Designer' glucocorticoids promise to be a great new advance in the therapy of inflammatory diseases. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:247 / 260
页数:14
相关论文
共 74 条
[1]  
AMEZAGA MA, 1992, BLOOD, V79, P735
[2]   A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotropin [J].
Annane, D ;
Sébille, V ;
Troché, G ;
Raphaël, JC ;
Gajdos, P ;
Bellissant, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (08) :1038-1045
[3]   Glucocorticoids in T cell development and function [J].
Ashwell, JD ;
Lu, FWM ;
Vacchio, MS .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :309-345
[4]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[5]   GLUCOCORTICOID RECEPTOR-BETA, A POTENTIAL ENDOGENOUS INHIBITOR OF GLUCOCORTICOID ACTION IN HUMANS [J].
BAMBERGER, CM ;
BAMBERGER, AM ;
DECASTRO, M ;
CHROUSOS, GP .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2435-2441
[6]   Dissociative glucocorticoid activity of medroxyprogesterone acetate in normal human lymphocytes [J].
Bamberger, CM ;
Else, T ;
Bamberger, AM ;
Beil, FU ;
Schulte, HM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (11) :4055-4061
[7]   Molecular determinants of glucocorticoid receptor function and tissue sensitivity to glucocorticoids [J].
Bamberger, CM ;
Schulte, HM ;
Chrousos, GP .
ENDOCRINE REVIEWS, 1996, 17 (03) :245-261
[8]   Corticosteroids, IgE, and atopy [J].
Barnes, PJ .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (03) :265-266
[9]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[10]  
BARNES PJ, 1995, AM J RESP CRIT CARE, V152, P125