n端肽免疫制备抗人CCR2单克隆抗体(C2Mab-9)

Q3 Medicine
Tomohiro Tanaka, Guanjie Li, Masaki Saito, Hiroyuki Suzuki, Teizo Asano, Mika K Kaneko, Yukinari Kato
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引用次数: 6

摘要

CC趋化因子受体2型(CCR2)是G蛋白偶联受体超家族的成员之一,在免疫细胞和肿瘤细胞表面表达。CCR2结合C-C基序趋化因子配体2 (CCL2)/单核细胞趋化蛋白-1 (MCP-1),由多种细胞产生,包括肿瘤和免疫相关细胞。因此,开发针对CCR2的敏感单克隆抗体(mab)已被用于治疗和诊断。本研究采用合成肽免疫的方法,建立了特异性抗人CCR2 (hCCR2)单抗、C2Mab-9(小鼠IgG1、kappa)单抗。流式细胞术和免疫细胞化学结果显示,C2Mab-9与表达hccr2的U937(人组织细胞淋巴瘤)和自然杀伤细胞发生反应。此外,C2Mab-9对这两种细胞均表现出中等的结合亲和力。总之,C2Mab-9可以成为分析hccr2相关生物学反应的有用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an Anti-human CCR2 Monoclonal Antibody (C2Mab-9) by N-Terminal Peptide Immunization.

The CC chemokine receptor type-2 (CCR2) is one of the members of the G protein-coupled receptor superfamily, which are expressed on the cell surface of immune and tumor cells. CCR2 binds to the C-C motif chemokine ligand 2 (CCL2)/monocyte chemoattractant protein-1 (MCP-1), which is produced by various cells, including tumor and immune-related cells. Therefore, the development of sensitive monoclonal antibodies (mAbs) for CCR2 has been desired for treatment and diagnosis. In this study, we established a specific antihuman CCR2 (hCCR2) mAb, C2Mab-9 (mouse IgG1, kappa), using the synthetic peptide immunization method. Flow cytometric and immunocytochemical results showed that C2Mab-9 reacted with hCCR2-expressing U937 (human histiocytic lymphoma) and natural killer cells. Furthermore, C2Mab-9 showed the moderate binding affinity for both cells. Conclusively, C2Mab-9 can be a useful tool for analyzing hCCR2-related biological responses.

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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
49
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