Cytokine profile of the rheumatoid nodule suggests that it is a Th1 granuloma

被引:65
作者
Hessian, PA [1 ]
Highton, J [1 ]
Kean, A [1 ]
Sun, CK [1 ]
Chin, M [1 ]
机构
[1] Univ Otago, Otago Med Sch, Dunedin, New Zealand
来源
ARTHRITIS AND RHEUMATISM | 2003年 / 48卷 / 02期
关键词
D O I
10.1002/art.10776
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To define the cytokine profile within rheumatoid subcutaneous nodules, and to determine whether the destructive inflammatory process in this lesion displays features of a lymphocyte-driven Th1 or Th2 granuloma. Methods. Subcutaneous nodules excised from 10 patients with rheumatoid arthritis were examined. Transcripts for interleukin 1beta (IL-lbeta) IL-2, IL-4, IL-5, IL-10, IL-12, IL-13, IL-15, IL-18, and for tumor necrosis factor alpha (TNFalpha) and interferon-gamma (IFNgamma) were detected by reverse transcription-polymerase chain reaction of extracted RNA. Results. Nine of 10 nodules contained transcripts for IFNgamma. We observed no evidence for the expression of IL-2, IL-4, or IL-5 among the lymphokine genes analyzed. Transcripts for TNFalpha, IL-1beta, IL-10, IL-15, and IL-18 were present in all 10 nodules. Transcripts for IL-12 were present in all but one nodule. Expression of IL-13 messenger RNA was observed in only 5 nodules. Conclusion. The cytokine profile within the rheumatoid nodule (i.e., presence of IFNgamma but not IL-2, and prominent expression of IL-1beta and TNFalpha together with IL-12, IL-18, IL-15, and IL-10) is similar to the profile of cytokines in the synovial lesion of rheumatoid arthritis, which is generally accepted as being attributable to a Th1-mediated inflammatory mechanism. Our results suggest that damage to affected synovial membrane or subcutaneous tissue is caused by the same inflammatory mechanisms, and that the nodule is a Th1 granuloma.
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页码:334 / 338
页数:5
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共 20 条
[1]   New pathogenetic insights into the sarcoid granuloma [J].
Agostini, C ;
Adami, F ;
Semenzato, G .
CURRENT OPINION IN RHEUMATOLOGY, 2000, 12 (01) :71-76
[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]  
DeKeyser F, 1997, J RHEUMATOL, V24, P1685
[4]  
Elewaut D, 2000, CLIN EXP RHEUMATOL, V18, P201
[5]   Immunopathology of schistosomiasis: a cautionary tale of mice and men [J].
Fallon, PG .
IMMUNOLOGY TODAY, 2000, 21 (01) :29-35
[6]  
HIGHTON J, 1990, J RHEUMATOL, V17, P1130
[7]  
Highton J, 2000, J RHEUMATOL, V27, P339
[8]  
JANOSSY G, 1981, LANCET, V2, P839
[9]   Interleukin 18: a pleiotropic participant in chronic inflammation [J].
McInnes, IB ;
Gracie, JA ;
Leung, BP ;
Wei, XQ ;
Liew, FY .
IMMUNOLOGY TODAY, 2000, 21 (07) :312-315
[10]   Interleukin-15 mediates T cell-dependent regulation of tumor necrosis factor-alpha production in rheumatoid arthritis [J].
McInnes, IB ;
Leung, BP ;
Sturrock, RD ;
Field, M ;
Liew, FY .
NATURE MEDICINE, 1997, 3 (02) :189-195