Abstract
We investigated the expression of intercellular adhesion molecules ICAM-1 and ICAM-3 on peripheral blood mononuclear cells in a subgroup of 34 patients with relapsing-remitting multiple sclerosis who were treated orally with the chemokine receptor 1 antagonist BX 471 in a 16-week, randomised, double-blind, placebo-controlled phase II study. ICAM-1 and ICAM-3 expression was measured by flow cytometry at different time points during and after therapy and compared using multivariate analysis of variance and non-parametric Mann Whitney test. ICAM-3 expression on CD14( +) peripheral blood mononuclear cells was increased in the verum group under therapy, but did not differ significantly between the verum and placebo groups. Most likely, this trend represents a small epiphenomenon only mediated by receptor cross-talk and feedback mechanisms.
Publication types
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Clinical Trial, Phase II
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Multicenter Study
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Randomized Controlled Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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Administration, Oral
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Antigens, CD / blood*
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Cell Adhesion Molecules / blood*
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Double-Blind Method
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Flow Cytometry
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Germany
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Humans
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Immunologic Factors / administration & dosage*
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Intercellular Adhesion Molecule-1 / blood
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Italy
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Leukocytes, Mononuclear / drug effects*
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Leukocytes, Mononuclear / immunology
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Lipopolysaccharide Receptors / blood
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Multiple Sclerosis, Relapsing-Remitting / drug therapy*
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Multiple Sclerosis, Relapsing-Remitting / immunology
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Phenylurea Compounds / administration & dosage*
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Piperidines / administration & dosage*
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Receptors, CCR1 / antagonists & inhibitors*
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Time Factors
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Treatment Outcome
Substances
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Antigens, CD
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CCR1 protein, human
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Cell Adhesion Molecules
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ICAM3 protein, human
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Immunologic Factors
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Lipopolysaccharide Receptors
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Phenylurea Compounds
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Piperidines
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Receptors, CCR1
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Intercellular Adhesion Molecule-1
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BX 471