Kanoh Y, Yunoki M, Taniguchi T, Suzuki Y, Ideno S, Morita E, Hirama M, Yokoyama K, Yamanishi K
Central Research Laboratories, Green Cross Corporation, Hirakata, Japan.
Hybridoma. 1992 Oct;11(5):569-79. doi: 10.1089/hyb.1992.11.569.
Human monoclonal antibodies (HMAbs) against human cytomegalovirus (HCMV) have been developed by fusion of human spleen cells and human lymphoblastoid cell lines (NP101 and NP197). The cell line NP101 had great advantages in its high fusion frequency and the stability of the resultant hybridomas. The specificity of HMAbs was confirmed by enzyme-linked immunosorbent assay (ELISA) and immunofluorescence staining. Two of the six HMAbs obtained, which were IgG3 subclass, neutralized viral infectivity in the absence of complement. The neutralizing activity of one of these two HMAbs was enhanced in the presence of human complement, whereas the other was not. Another IgG1 subclass HMAb neutralized viral infection only in the presence of complement. The remaining three HMAbs showed no neutralizing activity. Those HMAbs may provide an important approach to studying human immune responses to HCMV. HMAbs having neutralizing activity may prove to be useful for passive immunotherapy of HCMV diseases.
通过将人脾细胞与人淋巴母细胞系(NP101和NP197)融合,已开发出针对人巨细胞病毒(HCMV)的人单克隆抗体(HMAb)。细胞系NP101在其高融合频率和所得杂交瘤的稳定性方面具有很大优势。通过酶联免疫吸附测定(ELISA)和免疫荧光染色证实了HMAb的特异性。获得的六种HMAb中有两种属于IgG3亚类,在无补体的情况下中和病毒感染性。这两种HMAb中的一种在人补体存在下中和活性增强,而另一种则没有。另一种IgG1亚类HMAb仅在补体存在下中和病毒感染。其余三种HMAb未显示中和活性。这些HMAb可能为研究人类对HCMV的免疫反应提供重要方法。具有中和活性的HMAb可能被证明对HCMV疾病的被动免疫治疗有用。