Cx3Mab-4:用于流式细胞仪的新型抗小鼠 CXCR3 单克隆抗体。

Q3 Medicine
Tsunenori Ouchida, Yu Isoda, Tomohiro Tanaka, Mika K Kaneko, Hiroyuki Suzuki, Yukinari Kato
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引用次数: 0

摘要

C-X-C motif趋化因子受体 3(CXCR3,CD183)是 CXCL9、CXCL10 和 CXCL11 的 G 蛋白偶联受体。CXCR3 可诱导免疫细胞趋化并促进炎症。目前已开发出各种小鼠模型来模拟疾病的发病机制,并用于评估这些疾病的治疗方法。尽管 CXCR3 是抑制炎症的一个有吸引力的靶点,但抗 CXCR3 治疗药物尚未获得批准。在这项研究中,我们利用细胞免疫和筛选方法建立了一种新型抗小鼠 CXCR3(mCXCR3)单克隆抗体 Cx3Mab-4(大鼠 IgG1,kappa)。流式细胞仪分析表明,Cx3Mab-4 与过表达 mCXCR3 的中国仓鼠卵巢-K1(CHO/mCXCR3)细胞结合,但与亲代 CHO-K1 细胞无反应。经测定,Cx3Mab-4的解离常数为1.3×10-9 M,表明Cx3Mab-4对表达mCXCR3的细胞具有高亲和力。Cx3Mab-4可用于在临床前小鼠模型中靶向表达CXCR3的细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cx3Mab-4: A Novel Anti-Mouse CXCR3 Monoclonal Antibody for Flow Cytometry.

C-X-C motif chemokine receptor 3 (CXCR3, CD183) is a G-protein-coupled receptor for CXCL9, CXCL10, and CXCL11. CXCR3 induces chemotaxis of immune cells and promotes inflammation. Various mouse models have been developed to mimic the pathogenesis of diseases and used in the evaluation of therapeutics for these diseases. Although CXCR3 is an attractive target to suppress inflammation, anti-CXCR3 therapeutic agents have not been approved. In this study, we established a novel anti-mouse CXCR3 (mCXCR3) monoclonal antibody, Cx3Mab-4 (rat IgG1, kappa), using the Cell-Based Immunization and Screening method. Flow cytometric analysis demonstrated that Cx3Mab-4 bound to mCXCR3-overexpressed Chinese hamster ovary-K1 (CHO/mCXCR3) cells, but did not react to parental CHO-K1 cells. The dissociation constant of Cx3Mab-4 was determined as 1.3 × 10-9 M, indicating that Cx3Mab-4 possesses a high affinity to mCXCR3-expressing cells. Cx3Mab-4 could be useful for targeting CXCR3-expressing cells in preclinical mouse models.

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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
49
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