Effect of recombinant human interleukin 2 on neutrophil adherence to endothelial cells in vitro
Identifieur interne : 003E51 ( Main/Exploration ); précédent : 003E50; suivant : 003E52Effect of recombinant human interleukin 2 on neutrophil adherence to endothelial cells in vitro
Auteurs : Jun Li [Canada] ; Steve Gyorffy [Canada] ; Sharon Lee [Canada] ; Cheuk S. Kwok [Canada]Source :
- Inflammation [ 0360-3997 ] ; 1996-08-01.
Abstract
Abstract: Human neutrophils were demonstrated to possess interleukin-2 receptor (IL-2R)β andγ chains, notα chain and the binding of IL-2 to the IL-2Rβ chain on neutrophils plays an important regulatory role in neutrophil functions. We have investigated in this study the hypothesis that recombinant human IL-2(rhIL-2) can directly activate human neutrophils and increase their adherence to human umbilical vein endothelial cells (HUVEC). In an in vitro microtiter adherence assay, rhIL-2 significantly stimulated neutrophil adherence to HUVEC in a dose- and time-dependent manner. rhILI-2 concentration at 2000 u/ml and 2 hour incubation gave the best neutrophil stimulation. Treatment of neutrophils with rhIL-2 increased the expression of adhesion molecule CD18. Pretreatment of the stimulated neutrophils with a blocking monoclonal antibody to CD18 decreased but not completely blocked the adherence of neutrophils to HUVEC. These data suggest that rhIL-2 can directly stimulate and increase neutrophil adherence to HUVEC by enhancing the expression of CD18 and possibly other adhesion molecules on neutrophil surface. This may be a critical step in the early stage of the vascular leak syndrome (VLS) associated with high dose IL-2 therapy.
Url:
DOI: 10.1007/BF01486739
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: Human neutrophils were demonstrated to possess interleukin-2 receptor (IL-2R)β andγ chains, notα chain and the binding of IL-2 to the IL-2Rβ chain on neutrophils plays an important regulatory role in neutrophil functions. We have investigated in this study the hypothesis that recombinant human IL-2(rhIL-2) can directly activate human neutrophils and increase their adherence to human umbilical vein endothelial cells (HUVEC). In an in vitro microtiter adherence assay, rhIL-2 significantly stimulated neutrophil adherence to HUVEC in a dose- and time-dependent manner. rhILI-2 concentration at 2000 u/ml and 2 hour incubation gave the best neutrophil stimulation. Treatment of neutrophils with rhIL-2 increased the expression of adhesion molecule CD18. Pretreatment of the stimulated neutrophils with a blocking monoclonal antibody to CD18 decreased but not completely blocked the adherence of neutrophils to HUVEC. These data suggest that rhIL-2 can directly stimulate and increase neutrophil adherence to HUVEC by enhancing the expression of CD18 and possibly other adhesion molecules on neutrophil surface. This may be a critical step in the early stage of the vascular leak syndrome (VLS) associated with high dose IL-2 therapy.</div>
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