Abstract
The ability of cetirizine, a novel antihistamine agent, to inhibit the in vivo activation of human eosinophils, neutrophils and monocytes has been investigated using C3b- and IgG-dependent rosette formation, cytotoxicity against opsonised parasitic larvae and adherence to plasma-coated glass (PCG). The drug inhibited platelet-activating factor (PAF)-induced enhancement of eosinophil and neutrophil IgG (Fc) and complement (C3b) rosettes with an IC50 of 2 x 10(-5) M. There was also comparable inhibition of PAF-dependent enhancement of eosinophil cytotoxicity (for complement-coated schistosomula of Schistosoma mansoni). Cetirizine inhibited PAF-induced eosinophil, but not neutrophil, hyperadherence to PCG. These data support the view that cetirizine may exert some of its anti-allergic effects by inhibiting the activation of human granulocytes and that it may also selectively inhibit PAF-induced eosinophil hyperadherence.
Original language | English |
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Pages (from-to) | 158-162 |
Number of pages | 5 |
Journal | International Archives of Allergy and Applied Immunology |
Volume | 95 |
Issue number | 2-3 |
Publication status | Published - 1991 |
Keywords
- COMPLEMENT RECEPTORS
- CELLS-INVITRO
- EXPRESSION
- LEUKOCYTE
- ADHESION
- STIMULATION
- ENHANCEMENT
- ADHERENCE
- BINDING