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α干扰素与人骨肉瘤单克隆抗体791T/36的偶联

Interferon-alpha conjugation to human osteogenic sarcoma monoclonal antibody 791T/36.

作者信息

Pelham J M, Gray J D, Flannery G R, Pimm M V, Baldwin R W

出版信息

Cancer Immunol Immunother. 1983;15(3):210-6. doi: 10.1007/BF00199167.

Abstract

Human lymphoblastoid interferon-alpha (IFN-alpha) has been coupled using N-succinimidyl 3-(2-pyridyldithio) propionate (SPDP) to a murine monoclonal antibody (791T/36) which reacts with antigens expressed on human osteogenic sarcomas. The purified conjugates retain antibody activity as defined by their capacity to compete with binding of fluorescein isothiocyanate-labelled 791T/36 antibody to 791T cells. IFN-alpha-791T/36 antibody conjugates synthesized with 125I-trace-labelled IFN-alpha and 131I-trace-labelled antibody also bound to 791T cells, but not to bladder carcinoma T24 cells. The conjugates also retain the capacity of free IFN to activate natural killer cells in human peripheral blood lymphocytes and show specific localization in human osteogenic sarcoma xenografts developing in immunodeprived mice. These findings establish that conjugates containing IFN linked to a monoclonal antibody reacting with osteogenic sarcoma-associated antigens have potential for targeted immunotherapy and in related investigations with antibody has been shown by gamma camera imaging of patients following infusion of 131I-labelled antibody to localize in primary osteogenic sarcomas.

摘要

人淋巴母细胞干扰素-α(IFN-α)已使用N-琥珀酰亚胺基3-(2-吡啶基二硫代)丙酸酯(SPDP)与一种鼠单克隆抗体(791T/36)偶联,该抗体可与人骨肉瘤上表达的抗原发生反应。纯化后的偶联物保留了抗体活性,这可通过它们与异硫氰酸荧光素标记的791T/36抗体与791T细胞结合竞争的能力来定义。用125I标记的IFN-α和131I标记的抗体合成的IFN-α-791T/36抗体偶联物也能与791T细胞结合,但不与膀胱癌T24细胞结合。这些偶联物还保留了游离IFN激活人外周血淋巴细胞中自然杀伤细胞的能力,并在免疫缺陷小鼠中生长的人骨肉瘤异种移植物中显示出特异性定位。这些发现表明,含有与骨肉瘤相关抗原反应的单克隆抗体偶联的IFN的偶联物具有靶向免疫治疗的潜力,并且在相关研究中,通过对输注131I标记抗体后的患者进行γ相机成像,已显示抗体可在原发性骨肉瘤中定位。

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