The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis

被引:1872
作者
Fishman, D
Faulds, G
Jeffery, R
Mohamed-Ali, V
Yudkin, JS
Humphries, S
Woo, P
机构
[1] UCL, Sch Med, Windeyer Inst Med Sci, Paediat Rheumatol Unit, London W1P 6DB, England
[2] Rayne Inst, Ctr Genet Cardiovasc Disorders, London WC1E 6JJ, England
[3] Whittington Hosp, Dept Med, Ctr Diabet & Cardiovasc Risk, London N19 5UA, England
关键词
cytokine; SSCP; JCA; genetics; transfection;
D O I
10.1172/JCI2629
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
During active disease, patients with systemic-onset juvenile chronic arthritis (S-JCA) demonstrate a rise and fall in serum interleukin-6 (IL-6) that parallels the classic quotidian fever. To investigate the possibility that this cytokine profile results from a difference in the control of IL-6 expression, we examined the 5' flanking region of the IL-6 gene for polymorphisms. A G/C polymorphism was detected at position -174. In a group of 383 healthy men and women from a general practice in North London, the frequency of the C allele was 0.403 (95% confidence interval 0.37-0.44). In comparison, 92 patients with S-JCA had a different overall genotype frequency, especially those with onset of disease at < 5 yr of age. This was mainly due to the statistically significant lower frequency of the CC genotype in this subgroup. When comparing constructs of the 5' flanking region (-550-+61 bp) in a luciferase reporter vector transiently transfected into HeLa cells, the -174C construct showed 0.624+/-0.15-fold lower expression than the -174G construct. After stimulation with LPS or IL-1, expression from the -174C construct did not significantly change after 24 h, whereas expression from the -174G construct increased by 2.35+/-0.10- and 3.60+/-0.26-fold, respectively, compared with the unstimulated level. Plasma levels of IL-6 were also measured in 102 of the healthy subjects, and the C allele was found to be associated with significantly lower levels of plasma IL-6. These results suggest that there is a genetically determined difference in the degree of the IL-6 response to stressful stimuli between individuals. The reduced frequency of the potentially protective CC genotype in young S-JCA patients may contribute to its pathogenesis. Similarly the individual's IL-6 genotype may be highly relevant in other conditions where IL-6 has been implicated, such as atherosclerosis.
引用
收藏
页码:1369 / 1376
页数:8
相关论文
共 47 条
  • [1] ANGOTTI E, 1994, J BIOL CHEM, V269, P17371
  • [2] BOWCOCK A M, 1988, Genomics, V3, P8, DOI 10.1016/0888-7543(88)90152-8
  • [3] RAPID DETECTION AND SEQUENCING OF ALLELES IN THE 3' FLANKING REGION OF THE INTERLEUKIN-6 GENE
    BOWCOCK, AM
    RAY, A
    ERLICH, H
    SEHGAL, PB
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (17) : 6855 - 6864
  • [4] POLYMORPHISM IN TUMOR-NECROSIS-FACTOR GENES ASSOCIATED WITH MUCOCUTANEOUS LEISHMANIASIS
    CABRERA, M
    SHAW, MA
    SHARPLES, C
    WILLIAMS, H
    CASTES, M
    CONVIT, J
    BLACKWELL, JM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) : 1259 - 1264
  • [5] ETHNIC-DIFFERENCES IN FASTING PLASMA C-PEPTIDE AND INSULIN IN RELATION TO GLUCOSE-TOLERANCE AND BLOOD-PRESSURE
    CRUICKSHANK, JK
    COOPER, J
    BURNETT, M
    MACDUFF, J
    DRUBRA, U
    [J]. LANCET, 1991, 338 (8771) : 842 - 847
  • [6] DANIS VA, 1995, CLIN EXP IMMUNOL, V99, P303
  • [7] DAO DD, 1994, LEUKEMIA, V8, P1280
  • [8] ELECTROPHORESIS FOR GENOTYPING - MICROTITER ARRAY DIAGONAL GEL-ELECTROPHORESIS ON HORIZONTAL POLYACRYLAMIDE GELS, HYDROLINK, OR AGAROSE
    DAY, INM
    HUMPHRIES, SE
    [J]. ANALYTICAL BIOCHEMISTRY, 1994, 222 (02) : 389 - 395
  • [9] DEBenedetti F, 1995, CLIN EXP RHEUMATOL, V13, P779
  • [10] CORRELATION OF SERUM INTERLEUKIN-6 LEVELS WITH JOINT INVOLVEMENT AND THROMBOCYTOSIS IN SYSTEMIC JUVENILE RHEUMATOID-ARTHRITIS
    DEBENEDETTI, F
    MASSA, M
    ROBBIONI, P
    RAVELLI, A
    BURGIO, GR
    MARTINI, A
    [J]. ARTHRITIS AND RHEUMATISM, 1991, 34 (09): : 1158 - 1163