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The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics

机译:新型非小细胞肺癌特异性单克隆抗体NJ001及其生物学特性的研究

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摘要

Monoclonal antibody (McAb) is the key tool for cancer immunodiagnosis and immunotherapy. McAb-based immunotherapy that targets tumor antigens has had great achivement. In this study, a cell clone which kept secreting high-titer IgG1-type McAb named NJ001 against human non-small cell lung cancer (NSCLC) cells was obtained. The titer of purified NJ001 was 2×106. The antigen named SP70 of NSCLC specifically identified by NJ001 was proved to be a protein with the relative molecular mass (Mr) of 70 kDa. The results of immunohistochemical staining indicated that NJ001 could positively react to NSCLC, but weak positively or negatively react to human small-cell lung cancer (SCLC), pulmonary pseudotumor and other epithelial tumors. In soft agar assay, the colony formation efficiency in NJ001 groups decreased in a dose-dependent manner. For the concentration of 100 µg/ml, 200 µg/ml and 400 µg/ml, the inhibition ratio of colony formation was 23.4%, 62.5% and 100% respectively. Meanwhile, NJ001 caused significant reduction in tumor volume and tumor weight compared to control mice in lung cancer xenograft model. The tumor growth inhibition ratio in 200 µg, 400 µg and 800 µg NJ001 groups was 10.44%, 37.29% and 44.04%, respectively. NJ001 also led to cytomorphological changes and induced the apoptosis of human lung adenocarcinoma cell line SPC-A1 significantly. The newly developed NJ001 selectively reacted to NSCLC and exhibited anti-tumor activity both in vitro and in vivo. NJ001 is of great value concerning immunodiagnostics and immunotherapy for NSCLC and holds promise for further research regarding the mechanism underlying tumor progression of NSCLC.
机译:单克隆抗体(McAb)是癌症免疫诊断和免疫疗法的关键工具。针对肿瘤抗原的基于单克隆抗体的免疫疗法取得了巨大的成就。在这项研究中,获得了一种细胞克隆,该克隆持续分泌抗人非小细胞肺癌(NSCLC)细胞的高滴度IgG1型单克隆抗体NJ001。纯化的NJ001的效价为2×10 6 。由NJ001特异性鉴定的名为NSCLC的SP70抗原被证明是相对分子质量(Mr)为70 kDa的蛋白质。免疫组织化学染色结果表明,NJ001对NSCLC呈阳性反应,对人小细胞肺癌(SCLC),肺假瘤和其他上皮性肿瘤呈弱或阳性反应。在软琼脂分析中,NJ001组的菌落形成效率以剂量依赖性方式降低。对于100μg/ ml,200μg/ ml和400μg/ ml的浓度,菌落形成的抑制率分别为23.4%,62.5%和100%。同时,在肺癌异种移植模型中,与对照小鼠相比,NJ001导致肿瘤体积和肿瘤重量显着减少。 200μg,400μg和800μgNJ001组的肿瘤生长抑制率分别为10.44%,37.29%和44.04%。 NJ001还导致细胞形态学改变并显着诱导人肺腺癌细胞系SPC-A1凋亡。新开发的NJ001与NSCLC选择性反应,并在体内和体外均表现出抗肿瘤活性。 NJ001在NSCLC的免疫诊断和免疫治疗方面具有重要价值,并有望进一步研究NSCLC肿瘤进展的潜在机制。

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