Suppressive effects of co-stimulatory molecule expressions on mouse splenocytes by anti-allergic agents in vitro
THE influence of anti-allergic drugs, epinastine hydrochloride (EP) and disodium cromoglycate (DSCG), on the co-stimulatory molecule expression was examined using in vitro cell culture technique. Spleen cells obtained from BALB/c mice 10 days after immunization with haemocyanin absorbed to aluminium...
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Published in | Mediators of Inflammation Vol. 2000; no. 2; pp. 69 - 75 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Hindawi Limiteds
01.01.2000
Hindawi Limited |
Subjects | |
Online Access | Get full text |
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Summary: | THE influence of anti-allergic drugs, epinastine hydrochloride (EP) and disodium cromoglycate (DSCG), on the co-stimulatory molecule expression was examined using in vitro cell culture technique. Spleen cells obtained from BALB/c mice 10 days after immunization with haemocyanin absorbed to aluminium hydroxide were cultured in the presence of 100.0 μg /ml haemocyanin and various concentrations of the agents. Low concentrations (<1.5x10^(-4) M) of EP and DSCG did not influence spleen cell blastic activity induced by antigenic stimulation, whereas these agents caused significant inhibition of spleen cell activation when 2x10^(-4) M of the agents were added to cell cultures . EP and DSCG also did not affect blastic activity of sensitized splenic T cells by anti-CD3 monoclonal antibody stimulation even when these cells were cultured in the presence of 2x10^(-4)M of the agents. We next examined the influence of EP and DSCG on the expression of co-stimulatory molecule s on spleen cells in response to antigenic stimulation. Sensitized spleen cells were cultured in the presence of 2 x10^(-4)M of the agents and the expression of molecules were examined by flow cytometer 24 h later. EP and DSCG suppressed the expression of costimulatory molecule, CD40 and CD80, but not CD86, on splenic B cells which were enhanced by antigenic stimulation in vitro. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0962-9351 1466-1861 |
DOI: | 10.1080/096293500411523 |