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新型钙库操纵性钙通道阻滞剂YM-58483/BTP2对体内T细胞介导的免疫反应的特性研究

Characterization of YM-58483/BTP2, a novel store-operated Ca2+ entry blocker, on T cell-mediated immune responses in vivo.

作者信息

Ohga Keiko, Takezawa Ryuichi, Arakida Yasuhito, Shimizu Yasuaki, Ishikawa Jun

机构信息

Pharmacology Research Labs, Drug Discovery Research, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba-shi, Ibaraki 305-8585, Japan.

出版信息

Int Immunopharmacol. 2008 Dec 20;8(13-14):1787-92. doi: 10.1016/j.intimp.2008.08.016. Epub 2008 Sep 13.

DOI:10.1016/j.intimp.2008.08.016
PMID:18793756
Abstract

YM-58483/BTP2 is a blocker of store-operated Ca2+ entry (SOCE), which regulates the activation of non-excitable cells such as lymphocytes. YM-58483 has been reported to inhibit cytokine production and proliferation in T cells, and to be useful as a probable medicinal candidate for treatment of bronchial asthma. The present study investigated the pharmacological profile and therapeutic potential of YM-58483 in relation to cell-mediated immune responses. In the mouse graft-versus-host disease (GVHD) model, YM-58483 (1-30 mg/kg, p.o.) and cyclosporine A (1-30 mg/kg, p.o.) inhibited donor anti-host cytotoxic T lymphocyte (CTL) activity and IFN-gamma production, and also reduced the number of donor T cells, especially donor CD8+ T cells, in the spleen. YM-58483 and cyclosporine A inhibited T cell proliferation in a one-way mixed lymphocyte reaction (MLR) with IC50 values of 330 and 12.7 nM, respectively. Additionally, YM-58483 (1-10 mg/kg, p.o.) and cyclosporine A (2, 10 mg/kg, p.o.) inhibited the sheep red blood cell (SRBC)-induced delayed type hypersensitivity (DTH) response. These results suggest that the inhibition of SOCE leads to the prevention of antigen-induced T cell responses, which participate in autoimmune diseases such as autoimmune hepatitis and rheumatoid arthritis.

摘要

YM-58483/BTP2是一种储存式Ca2+内流(SOCE)阻滞剂,SOCE可调节淋巴细胞等非兴奋性细胞的激活。据报道,YM-58483可抑制T细胞中细胞因子的产生和增殖,有望作为治疗支气管哮喘的候选药物。本研究调查了YM-58483在细胞介导的免疫反应方面的药理特性和治疗潜力。在小鼠移植物抗宿主病(GVHD)模型中,YM-58483(1-30毫克/千克,口服)和环孢素A(1-30毫克/千克,口服)可抑制供体抗宿主细胞毒性T淋巴细胞(CTL)活性和IFN-γ的产生,还可减少脾脏中供体T细胞的数量,尤其是供体CD8+T细胞的数量。YM-58483和环孢素A在单向混合淋巴细胞反应(MLR)中抑制T细胞增殖,IC50值分别为330和12.7纳摩尔。此外,YM-58483(1-10毫克/千克,口服)和环孢素A(2、10毫克/千克,口服)可抑制绵羊红细胞(SRBC)诱导的迟发型超敏反应(DTH)。这些结果表明,抑制SOCE可预防抗原诱导的T细胞反应,而这种反应参与了自身免疫性肝炎和类风湿关节炎等自身免疫性疾病。

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