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In vitro immunization of human peripheral blood lymphocytes: establishment of B cell lines secreting IgM specific for cholera toxin B subunit from lymphocytes stimulated with IL-2 and IL-4

机译:人外周血淋巴细胞的体外免疫:从IL-2和IL-4刺激的淋巴细胞中分泌分泌特异性针对霍乱毒素B亚基的IgM的B细胞系

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摘要

In vitro immunization (IVI) techniques have a great potential in the production of human monoclonal antibodies (MAbs) against various antigens. An IVI method of human peripheral blood lymphocytes (PBL) has been developed with a human lung adenocarcinoma cell line in our laboratory. Although several cancer specific human MAbs were successfully generated by using this IVI method, it was not available for soluble antigens, which prompted us to improve the method for generation of human MAbs against soluble antigens. IVI with soluble antigens was effectively caused by the addition of muramyl dipeptides, interleukin-2 and interleukin-4. It was found that the difference of sensitivity of lymphocytes depending upon donors could be overcome by finding the optimal concentrations of IL-2 and IL-4. IVI of human PBL was performed with cholera toxin B subunit (CTB) and the immunized B cells were transformed by Epstein-Barr virus. Anti-CTB antibody was detected using an indirect ELISA. B cells producing anti-CTB antibodies were directly cloned by a soft agar cloning method.
机译:体外免疫(IVI)技术在生产针对各种抗原的人单克隆抗体(MAb)方面具有巨大潜力。在我们的实验室中,人肺腺癌细胞系已经开发了一种人外周血淋巴细胞(PBL)的IVI方法。尽管通过使用这种IVI方法成功产生了几种癌症特异性人单克隆抗体,但可溶性抗原尚不可用,这促使我们改进了针对可溶性抗原的人单克隆抗体的制备方法。具有可溶性抗原的IVI有效地由添加了鼠李基二肽,白介素2和白介素4引起。已经发现,通过找到最佳的IL-2和IL-4浓度可以克服依赖于供体的淋巴细胞敏感性的差异。用霍乱毒素B亚基(CTB)进行人PBL的IVI,并用爱泼斯坦-巴尔病毒转化免疫的B细胞。使用间接ELISA检测抗CTB抗体。通过软琼脂克隆方法直接克隆产生抗CTB抗体的B细胞。

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