Distribution of interleukin-10 family cytokines in serum and synovial fluid of patients with inflammatory arthritis reveals different contribution to systemic and joint inflammation

被引:47
作者
Scrivo, R. [1 ]
Conigliaro, P. [2 ]
Riccieri, V. [1 ]
Di Franco, M. [1 ]
Alessandri, C. [1 ]
Spadaro, A. [1 ]
Perricone, R. [2 ]
Valesini, G. [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Med Interna & Specialita Med, I-00161 Rome, Italy
[2] Univ Tor Vergata, Dipartimento Med Sistemi Reumatol Immunol & Aller, Rome, Italy
关键词
IL-10 family cytokine; inflammatory arthritis; serum; synovial fluid; PLAQUE-TYPE PSORIASIS; RHEUMATOID-ARTHRITIS; IL-19; EXPRESSION; IL-20; RECEPTORS; CLASSIFICATION; CRITERIA; DISEASE; GENES;
D O I
10.1111/cei.12449
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
Evidence exists that interleukin (IL)-10 family cytokines may be involved in the pathogenesis of rheumatoid arthritis (RA). We sought to determine whether or not these cytokines are involved in psoriatic arthritis (PsA). We conducted a prospective study on patients with PsA, RA and osteoarthritis (OA); healthy controls (HC) were also included. We analysed IL-20, IL-24 and IL-19 serum and synovial fluid (SF) levels and change of serum levels following treatment with biological agents. IL-20 serum levels were increased in PsA and RA compared with OA patients and HC and with matched SF levels. IL-24 serum levels in PsA, RA and OA patients were higher than those in HC and also with respect to matched SF in PsA. IL-19 serum levels were higher in HC and OA compared with PsA and RA patients; IL-19 SF levels were higher in PsA and RA compared with OA patients, and in PsA compared with RA patients. PsA and RA patients showed a reduction of IL-19 serum levels after biological treatment. Therefore, IL-19 seems to be involved mainly in the joint inflammation, whereas IL-20 and IL-24 appear to participate mainly in the systemic responses. These findings may further the comprehension of the contribution of these cytokines to the inflammatory response involved in chronic arthritis, as well as to the development of novel therapeutic strategies.
引用
收藏
页码:300 / 308
页数:9
相关论文
共 31 条
[1]
Expression of IL-10 family cytokines in rheumatoid arthritis: elevated levels of IL-19 in the joints [J].
Alanara, T. ;
Karstila, K. ;
Moilanen, T. ;
Silvennoinen, O. ;
Isomaki, P. .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2010, 39 (02) :118-126
[2]
THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]
Update on cytokines in rheumatoid arthritis [J].
Brennan, Fionula ;
Beech, Jonathan .
CURRENT OPINION IN RHEUMATOLOGY, 2007, 19 (03) :296-301
[4]
The extended IL-10 superfamily: IL-10, IL-19, IL-20, IL-22, IL-24, IL-26, IL-28, and IL-29 [J].
Commins, Scott ;
Steinke, John W. ;
Borish, Larry .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2008, 121 (05) :1108-1111
[5]
Cutting edge: STAT activation by IL-19, IL-20 and mda-7 through IL-20 receptor complexes of two types [J].
Dumoutier, L ;
Leemans, C ;
Lejeune, D ;
Kotenko, SV ;
Renauld, JC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3545-3549
[6]
Feldmann Marc, 1992, Progress in Growth Factor Research, V4, P247, DOI 10.1016/0955-2235(92)90022-A
[7]
Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2012 [J].
Furst, Daniel E. ;
Keystone, Edward Clark ;
So, Alexander K. ;
Braun, Juergen ;
Breedveld, Ferry C. ;
Burmester, Gerd R. ;
De Benedetti, Fabrizio ;
Doerner, Thomas ;
Emery, Paul ;
Fleischmann, Roy ;
Gibofsky, Allan ;
Kalden, J. R. ;
Kavanaugh, Arthur ;
Kirkham, Bruce ;
Mease, Philip ;
Rubbert-Roth, A. ;
Sieper, Joachim ;
Singer, Nora G. ;
Smolen, Josef S. ;
Van Riel, Piet L. C. M. ;
Weisman, Michael H. ;
Winthrop, Kevin L. .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 :2-34
[8]
Cloning, expression and initial characterisation of interleukin-19 (IL-19), a novel homologue of human interleukin-10 (IL-10) [J].
Gallagher, G ;
Dickensheets, H ;
Eskdale, J ;
Izotova, LS ;
Mirochnitchenko, OV ;
Peat, JD ;
Vazquez, N ;
Pestka, S ;
Donnelly, RP ;
Kotenko, SV .
GENES AND IMMUNITY, 2000, 1 (07) :442-450
[9]
Function of interleukin-20 as a proinflammatory molecule in rheumatoid and experimental arthritis [J].
Hsu, Yu-Hsiang ;
Li, Hsing-Hui ;
Hsieh, Mei-Yi ;
Liu, Ming-Fei ;
Huang, Kuo-Yuan ;
Chin, Lin-Show ;
Chen, Pei-Chih ;
Cheng, He-Hsiung ;
Chang, Ming-Shi .
ARTHRITIS AND RHEUMATISM, 2006, 54 (09) :2722-2733
[10]
Interleukin-19 blockade attenuates collagen-induced arthritis in rats [J].
Hsu, Yu-Hsiang ;
Hsieh, Pei-Pei ;
Chang, Ming-Shi .
RHEUMATOLOGY, 2012, 51 (03) :434-442