用于流式细胞术和免疫细胞化学的抗小鼠CCR8单克隆抗体(C8Mab-1)的研制

Masaki Saito, Hiroyuki Suzuki, Tomohiro Tanaka, Teizo Asano, Mika K Kaneko, Yukinari Kato
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引用次数: 8

摘要

单克隆抗体(mAb)作为肿瘤免疫治疗的有效工具已被广泛接受。C-C基序趋化因子受体8 (CCR8)在调节性T细胞和许多癌症中高度表达,并与癌症的进展有关。然而,它在癌症进展中的作用仍不清楚。因此,针对CCR8的单克隆抗体的开发导致癌症免疫治疗和对CCR8依赖性癌症进展的未知机制的阐明。在本研究中,我们利用细胞免疫和筛选(CBIS)方法开发了抗小鼠CCR8 (mCCR8)单抗(克隆C8Mab-1,大鼠IgG2a, kappa)。流式细胞术和免疫荧光显示,C8Mab-1及其重组抗体(recC8Mab-1)与mCCR8过表达的中国仓鼠卵巢(CHO)-K1细胞(CHO/mCCR8)结合,但与亲代CHO-K1细胞不结合。此外,在这两种应用中,C8Mab-1和rec8mab -1对表达内源性mCCR8的P388(小鼠淋巴细胞样细胞)和J774-1(小鼠巨噬细胞样细胞)都有特异性反应。这些结果表明,使用CBIS方法开发的C8Mab-1可用于针对外源性和内源性mCCR8的流式细胞术和免疫细胞化学。
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Development of an Anti-Mouse CCR8 Monoclonal Antibody (C8Mab-1) for Flow Cytometry and Immunocytochemistry.

It has been widely accepted that monoclonal antibody (mAb) is an effective tool for cancer immunotherapy. The C-C motif chemokine receptor 8 (CCR8) is highly expressed in regulatory T cells and many cancers and is associated with the progression of the cancers. However, its role in cancer progression remains unclear. Thus, the development of mAbs for CCR8 leads to cancer immunotherapy and elucidation of unknown mechanisms of CCR8-dependent cancer progression. In this study, we have developed an anti-mouse CCR8 (mCCR8) mAb (clone C8Mab-1, rat IgG2a, kappa) using the Cell-Based Immunization and Screening (CBIS) method. We showed that C8Mab-1 and its recombinant antibody (recC8Mab-1) bind to mCCR8-overexpressed Chinese hamster ovary (CHO)-K1 cells (CHO/mCCR8), but not to the parental CHO-K1 cells, in flow cytometry and immunofluorescence. Moreover, C8Mab-1 and recC8Mab-1 specifically reacted to P388 (a mouse lymphocyte-like cells) and J774-1 (a mouse macrophage-like cells), which express endogenous mCCR8, in both applications. These results suggest that C8Mab-1, developed using the CBIS method, is useful for flow cytometry and immunocytochemistry against exogenous and endogenous mCCR8.

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4.80
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发文量
49
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