Gimenez H B, Cash P, Melvin W T
J Gen Virol. 1984 May;65 ( Pt 5):963-71. doi: 10.1099/0022-1317-65-5-963.
Monoclonal antibodies to the RSN -2 isolate of human respiratory syncytial (RS) virus have been characterized with regard to their specificity for viral polypeptides and for different RS virus isolates. Five hybridoma antibodies recognized the phospho-protein VPP32 and the other recognized the matrix protein VPM27 . Evidence was obtained to support the view that VPP32 was associated with the nucleoprotein VPN41 . Three of the antibodies to VPP32 showed cytoplasmic immunofluorescent staining while the other two showed only surface staining of virus-infected cells. The immunoblot technique was used to determine the immunoreactivity of four of the hybridoma antibodies against human RS isolates other than RSN -2. One of these antibodies reacted exclusively with RSN -2 virus isolate whereas the others detected determinants shared by all human RS isolates tested. Extension of this approach may offer the possibility of typing RS isolates using monoclonal antibodies.
针对人类呼吸道合胞(RS)病毒RSN-2分离株的单克隆抗体,已就其对病毒多肽和不同RS病毒分离株的特异性进行了表征。五种杂交瘤抗体识别磷蛋白VPP32,其他抗体识别基质蛋白VPM27。有证据支持VPP32与核蛋白VPN41相关的观点。三种针对VPP32的抗体显示出细胞质免疫荧光染色,而另外两种仅显示病毒感染细胞的表面染色。免疫印迹技术用于确定四种杂交瘤抗体对RSN-2以外的人类RS分离株的免疫反应性。其中一种抗体仅与RSN-2病毒分离株反应,而其他抗体检测到所有测试的人类RS分离株共有的决定簇。这种方法的扩展可能提供使用单克隆抗体对RS分离株进行分型的可能性。