MISC

2005年8月

Suppressive activity of epinastine hydrochloride on TARC production from human peripheral blood CD4(+) T cells in-vitro

JOURNAL OF PHARMACY AND PHARMACOLOGY
  • K Kanai
  • ,
  • K Asano
  • ,
  • T Hisamitsu
  • ,
  • H Suzaki

57
8
開始ページ
1027
終了ページ
1035
記述言語
英語
掲載種別
DOI
10.1211/0022357056640
出版者・発行元
ROYAL PHARMACEUTICAL SOC GREAT BRITAIN

Thymus- and activation-regulated chemokine (TARC) is an important molecule in the development and maintenance of allergic diseases. However, there is little information about the influence of anti-allergic agents on TARC production. The aim of this study is to examine the influence of epinastine hydrochloride, an H-1-receptor antagonist, on TARC production from human peripheral blood CD4(+) T cells using an in-vitro cell culture technique. CD4(+) T cells prepared from healthy subjects were cultured in wells coated with a combination of OKT3 and anti-CD28 monoclonal antibody in the presence or absence of epinastine HCl for 24 h. The cells were also stimulated with interleukin (IL)-4 in a similar manner. Levels of TARC and IL-4 in culture supernatants were examined by ELISA. The addition of epinastine HCl exerted a dose-dependent suppressive effect on the production of both TARC and IL-4 from CD4(+) T cells under co-stimulatory molecule stimulation. The minimum concentration of the agent showing a significant suppressive effect on TARC and IL-4 production was 5.0 mu M and 2.5 mu M, respectively. Epinastine HCl also suppressed the ability of cells to produce TARC in response to IL-4 stimulation, when the agent was added to cell cultures at more than 2.5 mu M. It was concluded that this inhibitory action of epinastine HCl may be partially responsible for epinastine's attenuating effect on allergic diseases.

リンク情報
DOI
https://doi.org/10.1211/0022357056640
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000231032900011&DestApp=WOS_CPL
ID情報
  • DOI : 10.1211/0022357056640
  • ISSN : 0022-3573
  • Web of Science ID : WOS:000231032900011

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