Cytokine Dysregulation, Inflammation and Well-Being

NeuroImmunoModulation - Tập 12 Số 5 - Trang 255-269 - 2005
Ilia Elenkov1,2, Domenic G. Iezzoni3, Adrian Daly4, Alan G. Harris3, George P. Chrousos5
1Division of Rheumatology, Immunology and Allergy, Georgetown University Medical Center, Washington, D.C.,
2San Raffaele Research Center, Rome, Italy
3Integrated Therapeutics Group, Inc., a subsidiary of Schering-Plough Co., Kenilworth, N.J., and
4University of Liege, Liege, Belgium
5National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA

Tóm tắt

Cytokines mediate and control immune and inflammatory responses. Complex interactions exist between cytokines, inflammation and the adaptive responses in maintaining <i>homeostasis</i>, health, and well-being. Like the stress response, the inflammatory reaction is crucial for survival and is meant to be tailored to the stimulus and time. A full-fledged systemic inflammatory reaction results in stimulation of four major programs: the acute-phase reaction, the sickness syndrome, the pain program, and the stress response, mediated by the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system. Common human diseases such as atopy/allergy, autoimmunity, chronic infections and sepsis are characterized by a dysregulation of the pro- versus anti-inflammatory and T helper (Th)1versus Th2 cytokine balance. Recent evidence also indicates the involvement of pro-inflammatory cytokines in the pathogenesis of atherosclerosis and major depression, and conditions such as visceral-type obesity, metabolic syndrome and sleep disturbances. During inflammation, the activation of the stress system, through induction of a Th2 shift, protects the organism from systemic ‘overshooting’ with Th1/pro-inflammatory cytokines. Under certain conditions, however, stress hormones may actually facilitate inflammation through induction of interleukin (IL)-1, IL-6, IL-8, IL-18, tumor necrosis factor-α and C-reactive protein production and through activation of the corticotropin-releasing hormone/substance P-histamine axis. Thus, a dysfunctional neuroendocrine-immune interface associated with abnormalities of the ‘systemic anti-inflammatory feedback’ and/or ‘hyperactivity’ of the local pro-inflammatory factors may play a role in the pathogenesis of atopic/allergic and autoimmune diseases, obesity, depression, and atherosclerosis. These abnormalities and the failure of the adaptive systems to resolve inflammation affect the well-being of the individual, including behavioral parameters, quality of life and sleep, as well as indices of metabolic and cardiovascular health. These hypotheses require further investigation, but the answers should provide critical insights into mechanisms underlying a variety of common human immune-related diseases.

Từ khóa


Tài liệu tham khảo

10.1016%2F0167-5699%2896%2980606-2

10.1126%2Fscience.272.5258.50

10.1038%2Fnri1001

10.1016%2FS0167-5699%2899%2901535-2

10.1067%2Fmai.2001.112265

10.1067%2Fmai.2003.120

10.2500%2F108854101778148764

10.1016%2FS0091-6749%2800%2990177-5

10.1016%2FS0091-6749%2895%2970235-0

10.1084%2Fjem.187.4.537

10.1038%2Fnri1132

10.1080%2F00016350152509274

10.1016%2FS0016-5085%2899%2970392-6

10.1176%2Fappi.ajp.157.5.683

10.1016%2FS0753-3322%2801%2900156-1

10.1017%2FS1461145702003103

10.1016%2FS1471-4906%2802%2902331-1

10.1056%2FNEJMra021333

10.1016%2F0092-8674%2888%2990382-0

10.1016%2FS1043-2760%2899%2900188-5

10.1172%2FJCI119674

10.1016%2FS0165-5728%2898%2900073-3

10.1210%2Fjc.81.10.3604

10.1007%2FBF00228965

10.1016%2FS0165-5728%2898%2900109-X

10.1172%2FJCI118469

10.1016%2F0165-5728%2893%2990174-W

10.1016%2F0165-5728%2893%2990286-8

10.1038%2Fsj.bjp.0703134

10.1002%2F1521-4141%28200209%2932%3A9%3C2409%3A%3AAID-IMMU2409%3E3.0.CO%3B2-H

10.1172%2FJCI116884

10.1016%2F0192-0561%2894%2900096-7

10.1016%2F0167-5699%2892%2990057-E

10.1084%2Fjem.174.1.281

10.1067%2Fmai.2002.124044

10.1046%2Fj.1365-2249.1997.3791276.x

10.1126%2Fscience.2457950

10.1016%2FS0165-5728%2897%2900175-6

10.1111%2F1523-1747.ep12285627

10.1046%2Fj.1365-2567.2000.00082.x

10.1016%2FS1286-4579%2800%2901361-7

10.1038%2F35013070

10.1038%2Fnature01321

10.1046%2Fj.1365-2249.1996.29733.x

10.1172%2FJCI119314

10.1016%2FS0165-5728%2897%2900076-3

10.1210%2Fjc.86.12.5864

10.1038%2Fsj.ijo.0802035

10.1016%2F0167-5699%2894%2990137-6

10.1006%2Fmvre.2001.2304

10.1126%2Fscience.1925600

10.1111%2Fj.1749-6632.1999.tb07618.x

10.1210%2Fen.139.1.403

10.1210%2Fen.136.12.5745

10.1056%2FNEJM199505183322008

10.1111%2Fj.1749-6632.1998.tb09006.x

10.1210%2Fjc.82.4.1279

10.1210%2Fjc.84.8.2603

10.1210%2Fjc.85.3.1151

10.1053%2Fmeta.2002.33357

10.1210%2Fjc.82.5.1313

10.2500%2F108854100778248917

10.1067%2Fmai.2002.124776

10.1056%2FNEJM198007313030506

10.1172%2FJCI119674

10.1016%2F0091-6749%2894%2990044-2

10.1111%2Fj.1749-6632.1994.tb39788.x

10.1677%2Fjoe.0.1690429

10.1073%2Fpnas.86.12.4771

10.1073%2Fpnas.86.7.2374

10.1146%2Fannurev.iy.13.040195.001515

10.1111%2Fj.1749-6632.1999.tb07619.x

10.1002%2F1529-0131%28200103%2944%3A3%3C493%3A%3AAID-ANR95%3E3.0.CO%3B2-U

10.1002%2Fana.410270404

10.1111%2Fj.1749-6632.1988.tb27181.x

10.1016%2F0165-5728%2893%2990068-A

10.1111%2Fj.1749-6632.1988.tb27046.x

10.1096%2Ffj.99-1082com

10.1210%2Fjc.86.10.4933

10.1073%2Fpnas.97.1.325

10.1046%2Fj.1525-1381.1999.09423.x

10.1038%2Fsj.mp.4001032

10.1097%2F00003246-199304000-00015

10.1097%2F00003246-199501000-00015

10.1097%2F00000658-199522240-00006

10.1016%2FS0002-9610%2898%2900299-2

10.1038%2Fnm0798-808

10.1378%2Fchest.114.2.355-a

10.1097%2F00003246-199804000-00003

10.1126%2Fscience.280.5368.1432

10.1001%2Fjama.281.1.10

10.1056%2FNEJM199108293250903

10.1073%2Fpnas.221134198

10.1084%2Fjem.189.1.51

10.1016%2FS1471-4906%2801%2902090-7

10.1016%2FS0889-1591%2802%2900021-1

10.1016%2FS0022-3999%2801%2900302-6