The Regulation of Endotoxin Tolerance and its Impact on Macrophage Activation

被引:34
作者
Collins, Patricia E. [1 ]
Carmody, Ruaidhri J. [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Inst Infect Immun & Inflammat, Ctr Immunobiol, Glasgow G12 8TA, Lanark, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Endotoxin tolerance; Toll-like receptors; macrophage; inflammation; NF-KAPPA-B; COLONY-STIMULATING FACTOR; TUMOR-NECROSIS-FACTOR; INDUCED LEUCINE-ZIPPER; TOLL-LIKE RECEPTOR-4; ARYL-HYDROCARBON RECEPTOR; CYTOKINE SIGNALING SOCS; INDUCED SELF-TOLERANCE; ST2; GENE-PRODUCT; NEGATIVE REGULATOR;
D O I
10.1615/CritRevImmunol.2015015495
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Endotoxin tolerance in macrophages is a key regulatory mechanism to limit the innate immune response to infection or injury. Long considered a state of unresponsiveness to Toll-like receptor activation, tolerance is now recognized as a state of altered responsiveness to infection or injury. Endotoxin tolerance leads to a shift away from a pro-inflammatory response toward a response with key anti-inflammatory and pro-resolution features. Advances in our understanding of Toll-like receptor function have identified a number of molecular mechanisms that promote tolerance, but how these are integrated to achieve gene-specific regulation is an important outstanding question. The potential to harness the mechanisms of endotoxin tolerance to promote the resolution of chronic inflammation warrants the continued investigation of this fundamental feature of innate immunity. This review focuses on the endotoxin tolerant state, our understanding of the underlying molecular mechanisms, and the clinical significance of endotoxin tolerance.
引用
收藏
页码:293 / 323
页数:31
相关论文
共 227 条
[1]
Ubiquitin-mediated activation of TAK1 and IKK [J].
Adhikari, A. ;
Xu, M. ;
Chen, Z. J. .
ONCOGENE, 2007, 26 (22) :3214-3226
[2]
Gamma interferon and granulocyte/monocyte colony-stimulating factor prevent endotoxin tolerance in human monocytes by promoting interleukin-1 receptor-associated kinase expression and its association to MyD88 and not by modulating TLR4 expression [J].
Adib-Conquy, M ;
Cavaillon, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (31) :27927-27934
[3]
Ajibade AA, 2012, IMMUNITY, V36, P43, DOI 10.1016/j.immuni.2011.12.010
[4]
Suppressors of cytokine signalling (SOCS) in the immune system [J].
Alexander, WS .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (06) :410-416
[5]
ESTABLISHMENT OF DORSAL-VENTRAL POLARITY IN THE DROSOPHILA EMBRYO - GENETIC-STUDIES ON THE ROLE OF THE TOLL GENE-PRODUCT [J].
ANDERSON, KV ;
JURGENS, G ;
NUSSLEINVOLHARD, C .
CELL, 1985, 42 (03) :779-789
[6]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[8]
TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-1 LEAD TO PHOSPHORYLATION AND LOSS OF I-KAPPA-B-ALPHA - A MECHANISM FOR NF-KAPPA-B ACTIVATION [J].
BEG, AA ;
FINCO, TS ;
NANTERMET, PV ;
BALDWIN, AS .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) :3301-3310
[9]
Neurohormonal host defense in endotoxin shock [J].
Berczi, I .
NEUROIMMUNOMODULATION: MOLECULAR ASPECTS, INTEGRATIVE SYSTEMS, AND CLINICAL ADVANCES, 1998, 840 :787-802
[10]
INTERLEUKIN-10 IS A CENTRAL REGULATOR OF THE RESPONSE TO LPS IN MURINE MODELS OF ENDOTOXIC-SHOCK AND THE SHWARTZMAN REACTION BUT NOT ENDOTOXIN TOLERANCE [J].
BERG, DJ ;
KUHN, R ;
RAJEWSKY, K ;
MULLER, W ;
MENON, S ;
DAVIDSON, N ;
GRUNIG, G ;
RENNICK, D .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2339-2347