Bishop G A, Kümel G, Schwartz S A, Glorioso J C
J Virol. 1986 Jan;57(1):294-300. doi: 10.1128/JVI.57.1.294-300.1986.
The frequency and specificity of human cells with natural killer (NK) cytotoxic activity for herpes simplex virus type 1 (HSV-1)-infected targets was measured by limiting dilution culture. The frequency of NK cell precursors (NK-p) reactive with HSV-1-infected cells was 2- to 11-fold higher than that of NK-p reactive with mock-infected cells. The frequency of NK-p reactive with infected target cells lacking viral glycoprotein C or presenting an antigenically altered glycoprotein B was approximately twofold lower than that with wild-type virus-infected cells. Specificity analysis demonstrated that NK cells with a high statistical probability of being monoclonal were reactive with either glycoprotein B or C. These results provide the first evidence that cells with human NK activity possess clonal specificity for HSV-1-infected target cells.
通过有限稀释培养法测定了对1型单纯疱疹病毒(HSV-1)感染靶标具有自然杀伤(NK)细胞毒性活性的人细胞的频率和特异性。与HSV-1感染细胞反应的NK细胞前体(NK-p)的频率比与模拟感染细胞反应的NK-p高2至11倍。与缺乏病毒糖蛋白C或呈现抗原性改变的糖蛋白B的感染靶细胞反应的NK-p频率比与野生型病毒感染细胞反应的频率低约两倍。特异性分析表明,具有高统计学概率为单克隆的NK细胞与糖蛋白B或C反应。这些结果提供了首个证据,即具有人NK活性的细胞对HSV-1感染的靶细胞具有克隆特异性。