Jenkins D E, Yasukawa L L, Benike C J, Engleman E G, Arvin A M
Department of Pediatrics, Stanford University School of Medicine 94305, USA.
J Infect Dis. 1998 Nov;178 Suppl 1:S39-42. doi: 10.1086/514258.
A human dendritic cell-based assay used to monitor a T cell proliferation response to viral peptides in vitro is described. Dendritic cells and autologous CD4+ T cells were isolated from peripheral blood by a series of density-gradient centrifugations or magnetic bead separations (or both). Peptides corresponding to residues of the immediate early protein, IE62, of varicella-zoster virus (VZV) were used as stimulating antigens, and persons with no history of varicella and no humoral or cellular immunity to VZV served as naive donors for the assays. Three VZV-susceptible donors were tested, and all demonstrated an in vitro response to multiple VZV peptides. This assay has potential as a screen to establish the immunogenicity of viral antigens in vitro using T cells from naive donors.
本文描述了一种基于人树突状细胞的检测方法,用于在体外监测T细胞对病毒肽的增殖反应。通过一系列密度梯度离心或磁珠分离(或两者结合)从外周血中分离树突状细胞和自体CD4+ T细胞。将与水痘-带状疱疹病毒(VZV)即刻早期蛋白IE62残基对应的肽用作刺激抗原,无水痘病史且对VZV无体液或细胞免疫的人作为检测的初始供体。对三名VZV易感供体进行了检测,所有供体均表现出对多种VZV肽的体外反应。该检测方法有潜力作为一种筛选方法,利用初始供体的T细胞在体外确定病毒抗原的免疫原性。