SOLUBLE IMMUNOLOGICAL PRODUCTS IN SCLERODERMA SERA

被引:47
作者
KAHALEH, MB
机构
[1] Department of Medicine, Medical University of South Carolina, Charleston
来源
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1991年 / 58卷 / 01期
关键词
D O I
10.1016/0090-1229(91)90155-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To investigate the role of immune mechanisms in scleroderma (systemic sclerosis, SSc), we measured the levels of selected cytokines and soluble immune markers in patient sera. Forty-two patients and 14 matched healthy controls are the subject of this report. In the SSc group, tumor necrosis factor (TNF) was found in 8 42 (29 ± 539 pg/ml, meal level ± SD) and lymphotoxin in 36 42 (1:409-1:200, serum dilution). Interleukin β (IL-1β) was observed in 23 42 (44 ± 29, U/ml). IL-2 was identified in 36 42 patients with a mean level of 286 ± 406 U/ml, soluble interleukin-2 receptor in 42 42 (1055 ± 393, U/ml), soluble CD4 antigen in 27 42 (1:10-1:320, serum dilution), and CD8 in 42 42 (470 ± 134, U/mol). TNF, lymphotoxin, IL-1β, Il-2, and CD4 were not detected in the control group. IL-2 receptor levels in control subjects were 520 ± 171 U/ml, significantly lower than those of scleroderma (P < 0.001), and CD8 levels (582 ± 140) were significantly higher than in scleroderma (P < 0.05). The data suggest an ongoing activation of immune cells, particularly the CD4+ subset in SSc and indicate a potential role for the released mediator TNF, IL-1β, and lymphotoxin in the disease process. © 1991.
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页码:139 / 144
页数:6
相关论文
共 21 条
[1]   DECREASED PRODUCTION OF AND RESPONSE TO INTERLEUKIN-2 BY CULTURED LYMPHOCYTES FROM PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ALCOCERVARELA, J ;
ALARCONSEGOVIA, D .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 69 (06) :1388-1392
[2]   DIFFERENCES IN THE PRODUCTION OF AND OR THE RESPONSE TO INTERLEUKIN-2 BY LYMPHOCYTES-T FROM PATIENTS WITH THE VARIOUS CONNECTIVE-TISSUE DISEASES [J].
ALCOCERVARELA, J ;
LAFFON, A ;
ALARCONSEGOVIA, D .
RHEUMATOLOGY INTERNATIONAL, 1984, 4 (01) :39-44
[3]   A FUNCTIONAL DICHOTOMY IN CD4+ LYMPHOCYTES-T [J].
BOTTOMLY, K .
IMMUNOLOGY TODAY, 1988, 9 (09) :268-274
[4]  
BROWN M, 1987, FASEB J, V46, P467
[5]   PATHOLOGIC OBSERVATIONS CONCERNING THE CUTANEOUS LESION OF PROGRESSIVE SYSTEMIC SCLEROSIS - AN ELECTRON MICROSCOPIC HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL STUDY [J].
FISHER, ER ;
RODNAN, GP .
ARTHRITIS AND RHEUMATISM, 1960, 3 (06) :536-545
[6]   SCLERODERMA - A MODEL FOR FIBROSIS [J].
FLEISCHMAJER, R ;
PERLISH, JS ;
DUNCAN, M .
ARCHIVES OF DERMATOLOGY, 1983, 119 (12) :957-962
[7]   ULTRASTRUCTURE OF CUTANEOUS CELLULAR INFILTRATES IN SCLERODERMA [J].
FLEISCHMAJER, R ;
PERLISH, JS ;
WEST, WP .
ARCHIVES OF DERMATOLOGY, 1977, 113 (12) :1661-1666
[8]  
FLEISCHMAJER R, 1977, ARTHRITIS RHEUM, V20, P775
[9]  
FREUNDLICH B, 1987, CLIN EXP IMMUNOL, V69, P375
[10]  
ISHIDA H, 1987, J IMMUNOL, V139, P1070