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 inMediators of Inflammation Vol. 2000; no. 2; pp. 69 - 75
Main Authors Ito, J, Asano, K, Tryka, E, Kanai, K, Yamamoto, S, Hisamitsu, T, Suzaki, H
Format Journal Article
LanguageEnglish
Published United States Hindawi Limiteds 01.01.2000
Hindawi Limited
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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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ISSN:0962-9351
1466-1861
DOI:10.1080/096293500411523