人单克隆抗体识别人巨细胞病毒的早期和晚期病毒蛋白。

H. Alexander, J. Harpprecht, H. -. Podzuweit, P. Rautenberg, W. Müller‐ruchholtz
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引用次数: 5

摘要

将hcmv血清阳性的53岁器官供者体外刺激的人脾脏淋巴细胞与小鼠骨髓瘤细胞系Ag8.653融合,制备了人巨细胞病毒单克隆抗体。自1988年3月以来,通过ELISA技术筛选了14个产生抗巨细胞病毒IgG的人/小鼠杂交瘤,并建立了4个选择的克隆,每ml培养上清产生5-40微克/24 h的IgG。对照和局部巨细胞病毒株被抗体染色,与其他疱疹病毒无交叉反应。三种单克隆抗体A4B4 (IgG11)、A6B3 (IgG1k)和A6A2 (IgG1k)免疫沉淀了一个68 kDa的早期病毒蛋白,该蛋白在感染周期内首先出现在细胞核(18-24小时),然后出现在感染细胞的细胞质(24-96小时)。DNA复制的抑制限制了68 kDa病毒蛋白在感染细胞细胞核内的检测。未固定感染细胞的染色显示,两种抗体结合在少数细胞的表面。第4个单克隆抗体A3C5 (IgG11)免疫沉淀了一个34/38 kDa的晚期病毒蛋白,该蛋白出现在感染细胞的细胞核中(48-72 h)。这些抗体使我们能够研究人类宿主对人类巨细胞病毒的反应,并阐明人类抗体的功能,特别是它们与t细胞反应的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human monoclonal antibodies recognize early and late viral proteins of human cytomegalovirus.
Human monoclonal antibodies directed against human cytomegalovirus were generated by fusion of in vitro stimulated human spleen lymphocytes from an HCMV-seropositive 53-year-old organ donor with the mouse myeloma cell line Ag8.653. Fourteen human/mouse hybridomas producing anti-cytomegalovirus IgG were screened by an ELISA technique and four selected clones have been established since March 1988, generating about 5-40 micrograms/24 h IgG per ml culture supernatant. Reference and local cytomegalovirus strains were stained by the antibodies without showing cross-reactivity to other herpes viruses. Three monoclonal antibodies, A4B4 (IgG11), A6B3 (IgG1k) and A6A2 (IgG1k), immunoprecipitated a 68 kDa early viral protein which appears during the infectious cycle, first in the nucleus (18-24 h) and then also in the cytoplasm (24-96 h) of infected cells. Inhibition of DNA replication restricted the detection of the 68 kDa viral protein to the nucleus of infected cells. Staining of unfixed infected cells showed that two of the antibodies bound at the surface of a few cells. The fourth monoclonal antibody A3C5 (IgG11) immunoprecipitated a 34/38 kDa late viral protein which appears in the nucleus (48-72 h) of infected cells. These antibodies enable us to study the human host response to human cytomegalovirus and to elucidate the functions of human antibodies especially in their interaction with the T-cell response.
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