Increased expression of costimulatory molecules on peripheral blood monocytes in patients with Crohn's disease

Scand J Gastroenterol. 1997 Dec;32(12):1241-6. doi: 10.3109/00365529709028154.

Abstract

Background: Activation of T lymphocytes and monocytes/macrophages has been implicated in the pathogenesis of Crohn's disease (CD). Costimulatory molecules play important roles in optimal T-cell activation.

Methods: With flow cytometric analysis we have investigated the expression of the costimulatory molecules B7-1 (CD80), B7-2 (CD86), and CD18 and the intercellular adhesion molecule-1 (ICAM-1) on peripheral blood monocytes and the expression of the activation markers HLA-DR and IL-2R (CD25) on peripheral blood T lymphocytes from 31 CD patients, 17 ulcerative colitis (UC) patients, and 10 healthy controls.

Results: In CD patients the percentage of activated T cells (CD3+ HLA-DR+ and CD3+ IL-2R+) was significantly increased compared with those of controls and UC patients (P < 0.05). Most monocytes from all three groups expressed B7-2, CD18, and ICAM-1 molecules (all > 79%), but only a few positive cells expressed B7-1 molecules (< 5%). No significant differences were detected in the percentage positivity of all costimulatory molecules tested among CD, UC, and controls. The mean fluorescence intensity (MFI) of B7-1 in all three groups was very weak and not significantly different. However, in CD patients there was a significantly increased MFI of B7-2, CD18, and ICAM-1 molecules compared with UC and controls (P < 0.05). On the other hand, both the percentage positivity and MFI of HLA-DR molecules on monocytes of UC patients were significantly lower than those of CD patients and controls (P < 0.05).

Conclusions: Expression of the costimulatory molecules B7-2, CD18, and ICAM-1 on peripheral blood monocytes of CD patients is increased. In CD patients activation of peripheral T lymphocytes may correlate with increased expression of these costimulatory molecules on peripheral blood monocytes.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / metabolism
  • Antigens, Differentiation, T-Lymphocyte / metabolism*
  • B7-1 Antigen / metabolism
  • B7-2 Antigen
  • CD18 Antigens / metabolism
  • Colitis, Ulcerative / metabolism
  • Crohn Disease / metabolism*
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique, Direct
  • HLA-DR Antigens / metabolism
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Male
  • Membrane Glycoproteins / metabolism
  • Middle Aged
  • Monocytes / metabolism*
  • Receptors, Interleukin-2 / metabolism
  • T-Lymphocytes / metabolism*

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • B7-1 Antigen
  • B7-2 Antigen
  • CD18 Antigens
  • CD86 protein, human
  • HLA-DR Antigens
  • Membrane Glycoproteins
  • Receptors, Interleukin-2
  • Intercellular Adhesion Molecule-1