Induction of Interleukin-19 and Interleukin-22 After Cardiac Surgery With Cardiopulmonary Bypass

Annals of Thoracic Surgery

Volumn 81, Issue 6, 2006, Pages 2196-2201

  Hsing, Chung Hsi ^a,d   Hsieh, Mei Yi ^b   Chen, Wei Yu ^c   Cheung So, Edmund ^c,d   Cheng, Bor Chih ^c,d   Chang, Ming Shi ^a,e  

^a Institute of Biopharmaceutical Sciences   (Taiwan)

^b Institute of Biochemistry and Molecular Biology   (Taiwan)

^c NATIONAL CHENG KUNG UNIVERSITY   (Taiwan)

^d Department of Anesthesiology ^*  (Taiwan)

^e CHI MEI MEDICAL CENTER   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; INTERLEUKIN 10; INTERLEUKIN 19; INTERLEUKIN 20; INTERLEUKIN 22; INTERLEUKIN 6; TUMOR NECROSIS FACTOR ALPHA;

ADULT; AGED; ARTICLE; CARDIOPULMONARY BYPASS; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HEART SURGERY; HUMAN; IN VITRO STUDY; INFLAMMATION; MALE; MONOCYTE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

AGED; C-REACTIVE PROTEIN; CARDIOPULMONARY BYPASS; CELLS, CULTURED; CORONARY ARTERY BYPASS; CYTOKINES; DNA, COMPLEMENTARY; ENZYME-LINKED IMMUNOSORBENT ASSAY; EXTRACORPOREAL CIRCULATION; FEMALE; GENE EXPRESSION REGULATION; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; HUMANS; INTERLEUKIN-6; INTERLEUKINS; INTERNAL MAMMARY-CORONARY ARTERY ANASTOMOSIS; LIPOPOLYSACCHARIDES; MALE; MIDDLE AGED; MONOCYTES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SURGICAL PROCEDURES, ELECTIVE; SYSTEMIC INFLAMMATORY RESPONSE SYNDROME; TUMOR NECROSIS FACTOR-ALPHA;

EID: 33646828508     PISSN: 00034975     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.athoracsur.2006.01.092     Document Type: Article

References (29)

1. Jansen N.J., van Oeveren W., van den Broek L., et al. Inhibition by dexamethasone of the reperfusion phenomena in cardiopulmonary bypass. J Thorac Cardiovasc Surg 102 (1991) 515-525
2. Menasche P., Haydar S., Peynet J., et al. A potential mechanism of vasodilation after warm heart surgery. The temperature-dependent release of cytokines. J Thorac Cardiovasc Surg 107 (1994) 293-299
3. Finn A., Naik S., Klein N., et al. Interleukin-8 release and neutrophil degranulation after pediatric cardiopulmonary bypass. J Thorac Cardiovasc Surg 105 (1993) 234-241
4. Kawamura T., Wakusawa R., Okada K., and Inada S. Elevation of cytokines during open heart surgery with cardiopulmonary bypass. participation of interleukin 8 and 6 in reperfusion injury. Can J Anaesth 40 (1993) 1016-1021
5. Cremer J., Martin M., Redl H., et al. Systemic inflammatory response syndrome after cardiac operations. Ann Thorac Surg 61 (1996) 1714-1720
6. Edmunds Jr. L.H. Inflammatory response to cardiopulmonary bypass. Ann Thorac Surg 66 (1998) S12-6; discussion S25-8
7. Pestka S., Krause C.D., Sarkar D., et al. Interleukin-10 and related cytokines and receptors. Annu Rev Immunol 22 (2004) 929-979
8. Fickenscher H., Hor S., Kupers H., et al. The interleukin-10 family of cytokines. Trends Immunol 23 (2002) 89-96
9. Langer J.A., Cutrone E.C., and Kotenko S. The Class II cytokine receptor (CRF2) family. overview and patterns of receptor-ligand interactions. Cytokine Growth Factor Rev 15 (2004) 33-48
10. Wan S., LeClerc J.L., and Vincent J.L. Cytokine responses to cardiopulmonary bypass. lessons learned from cardiac transplantation. Ann Thorac Surg 63 (1997) 269-276
11. Giomarelli P., Scolletta S., Borrelli E., and Biagioli B. Myocardial and lung injury after cardiopulmonary bypass. role of interleukin (IL)-10. Ann Thorac Surg 76 (2003) 117-123
12. Conti P., Kempuraj D., Frydas S., et al. IL-10 subfamily members. IL-19, IL-20, IL-22, IL-24 and IL-26. Immunol Lett 88 (2003) 171-174
13. Zdanov A. Structural features of the interleukin-10 family of cytokines. Curr Pharm Des 10 (2004) 3873-3884
14. Liao Y.C., Liang W.G., Chen F.W., et al. IL-19 induces production of IL-6 and TNF-alpha and results in cell apoptosis through TNF-alpha. J Immunol 169 (2002) 4288-4297
15. Liao S.C., Cheng Y.C., Wang Y.C., et al. IL-19 induced Th2 cytokines and was up-regulated in asthma patients. J Immunol 173 (2004) 6712-6718
16. Rich B.E., and Kupper T.S. Cytokines. IL-20 - a new effector in skin inflammation. Curr Biol 11 (2001) R531-R534
17. Lejeune D., Dumoutier L., Constantinescu S., et al. Interleukin-22 (IL-22) activates the JAK/STAT, ERK, JNK, and p38 MAP kinase pathways in a rat hepatoma cell line. Pathways that are shared with and distinct from IL-10. J Biol Chem 277 (2002) 33676-33682
18. Wei C.C., Chen W.Y., Wang Y.C., et al. Detection of IL-20 and its receptors on psoriatic skin. Clin Immunol 117 (2005) 65-72
19. Li H.H., Lin Y.C., Chen P.J., et al. Interleukin-19 upregulates keratinocyte growth factor and is associated with psoriasis. British Journal of Dermatology 153 (2005) 591-595
20. Ikeuchi H., Kuroiwa T., Hiramatsu N., et al. Expression of interleukin-22 in rheumatoid arthritis. potential role as a proinflammatory cytokine. Arthritis Rheum 52 (2005) 1037-1046
21. Bourbon A., Vionnet M., Leprince P., et al. The effect of methylprednisolone treatment on the cardiopulmonary bypass-induced systemic inflammatory response. Eur J Cardiothorac Surg 26 (2004) 932-938
22. Volk T., Dopfmer U.R., Schmutzler M., et al. Stress induced IL-10 does not seem to be essential for early monocyte deactivation following cardiac surgery. Cytokine 24 (2003) 237-243
23. Butler J., Rocker G.M., and Westaby S. Inflammatory response to cardiopulmonary bypass. Ann Thorac Surg 55 (1993) 552-559
24. Oudemans-van Straaten H.M., Jansen P.G., Hoek F.J., et al. Intestinal permeability, circulating endotoxin, and postoperative systemic responses in cardiac surgery patients. J Cardiothorac Vasc Anesth 10 (1996) 187-194
25. Jordan W.J., Eskdale J., Boniotto M., et al. Human IL-19 regulates immunity through auto-induction of IL-19 and production of IL-10. Eur J Immunol 35 (2005) 1576-1582
26. Wolk K., Witte E., Reineke U., et al. Is there an interaction between interleukin-10 and interleukin-22?. Genes Immun 6 (2005) 8-18
27. Nagalakshmi M.L., Rascle A., Zurawski S., Menon S., and de Waal Malefyt R. Interleukin-22 activates STAT3 and induces IL-10 by colon epithelial cells. Int Immunopharmacol 4 (2004) 679-691
28. Wolk K., Kunz S., Asadullah K., and Sabat R. Cutting edge. immune cells as sources and targets of the IL-10 family members?. J Immunol 168 (2002) 5397-5402
29. Hennein H.A., Ebba H., Rodriguez J.L., et al. Relationship of the proinflammatory cytokines to myocardial ischemia and dysfunction after uncomplicated coronary revascularization. J Thorac Cardiovasc Surg 108 (1994) 626-635