Increased production of granulocyte-macrophage colony-stimulating factor in Crohn's disease - a possible target for infliximab treatment

被引:34
作者
Agnholt, J
Kelsen, J
Brandsborg, B
Jakobsen, NO
Dahlerup, JF
机构
[1] Aarhus Univ Hosp, Dept Med 5, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Pathol, DK-8000 Aarhus C, Denmark
关键词
Crohn's disease; GM-CSF; inflammation; neutrophils; cytokines;
D O I
10.1097/01.meg.0000108344.41221.8b
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The presence of neutrophils among epithelial cells is one of the major features of the inflammation in Crohn's disease, and has been used to indicate disease activity. The survival of neutrophils outside the blood vessels is limited and their longevity is influenced by granulocyte-macrophage colony-stimulating factor (GM-CSF), which probably reduces neutrophil apoptosis. Objective To study GM-CSF production in intestinal cell cultures from Crohn's disease patients before and after infliximab treatment. Patients Colonic mucosal biopsies were obtained from 29 Crohn's disease patients before and after three infliximab infusions (5 mg/ml) and from ten healthy subjects. disease patients compared with healthy controls (P=0.02) and correlated with the CDAI (Spearman rho = 0.65, P=0.001). GM-CSF levels and mucosal histology score decreased (P = 0.007 and P = 0.01 respectively) after three infliximab infusions, as did the peripheral blood leucocyte count (P < 0.001). Infliximab inhibited in-vitro T cell GM-CSF production. Methods Biopsies were cultured in RPMI at high concentrations of interleukin-2 (IL-2) (2000 U/ml) and IL-4 (500 U/ml), but without antigen addition. GM-CSF content was analysed after 5 days culture and related to the Crohn's disease activity index (CDAI) and compared with the GM-CSF production from healthy subjects. Peripheral leucocyte count, C-reactive protein and the degree of mucosal inflammation, evaluated histologically, were determined. In-vitro T cell GM-CSF production was; studied with/without addition of infliximab and after stimulation. Conclusion In-vitro cell culture production of GM-CSF was increased in Crohn's disease and related to inflammation, but decreased after infliximab treatment, probably because intestinal T cell GM-CSF production was reduced.
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页码:649 / 655
页数:7
相关论文
共 29 条
  • [1] In situ activated intestinal T cells expanded in vitro - without addition of antigen - produce IFN-γ and IL-10 and preserve their function during growth
    Agnholt, J
    Kaltoft, K
    [J]. EXPERIMENTAL AND CLINICAL IMMUNOGENETICS, 2001, 18 (04) : 213 - 225
  • [2] Infliximab downregulates interferon-γ production in activated gut T-lymphocytes from patients with Crohn's disease
    Agnholt, J
    Kaltoft, K
    [J]. CYTOKINE, 2001, 15 (04) : 212 - 222
  • [3] Tumor necrosis factor α antibody (infliximab) therapy profoundly down-regulates the inflammation in Crohn's ileocolitis
    Baert, FJ
    D'Haens, GR
    Peeters, M
    Hiele, MI
    Schaible, TF
    Shealy, D
    Geboes, K
    Rutgeerts, PJ
    [J]. GASTROENTEROLOGY, 1999, 116 (01) : 22 - 28
  • [4] BEST WR, 1976, GASTROENTEROLOGY, V70, P439
  • [5] Bregenholt S, 1998, CLIN EXP IMMUNOL, V111, P166
  • [6] Carlson M, 1999, AM J GASTROENTEROL, V94, P1876
  • [7] Human neutrophil lipocalin is a unique marker of neutrophil inflammation in ulcerative colitis and proctitis
    Carlson, M
    Raab, Y
    Sevéus, L
    Xu, S
    Hällgren, R
    Venge, P
    [J]. GUT, 2002, 50 (04) : 501 - 506
  • [8] Endoscopic and histological healing with infliximab anti-tumor necrosis factor antibodies in Crohn's disease: A European multicenter trial
    D'Haens, G
    Van Deventer, S
    Van Hogezand, R
    Chalmers, D
    Kothe, C
    Baert, F
    Braakman, T
    Schaible, T
    Geboes, K
    Rutgeerts, P
    [J]. GASTROENTEROLOGY, 1999, 116 (05) : 1029 - 1034
  • [9] Early lesions of recurrent Crohn's disease caused by infusion of intestinal contents in excluded ileum
    D'Haens, GR
    Geboes, K
    Peeters, M
    Baert, F
    Pennickx, F
    Rutgeerts, P
    [J]. GASTROENTEROLOGY, 1998, 114 (02) : 262 - 267
  • [10] Treatment of active Crohn's disease with recombinant human granulocyte-macrophage colony-stimulating factor
    Dieckgraefe, BK
    Korzenik, JR
    [J]. LANCET, 2002, 360 (9344) : 1478 - 1480