Regulation of the growth of epstein-barr virus-infected B cells: Temporal profile of the development of three distinct cytotoxic cells

The time course of the appearance of cytotoxic cells was examined in cocultures of E-rosetting (E+) cells and EBV-infected non-T cells (4:1 ratio) from the blood of VCA-positive healthy adults. Classical HNK-1+ NK cells were present at the initiation of the cultures and they produced 76 ± 2% specific 51Cr-release from K-562 cells, but they did not effectively lyse the NK-resistant Daudi cells, nor did they kill autologous EBV-induced lymphoblasts (LCLEBV). The NK activity decreased during the first week in culture to 40 ± 7% cytotoxicity. At the same time, nonspecific cytotoxic cells capable of killing Daudi as well as K562 developed and persisted into the third week in culture when it declined. This later nonspecific cytotoxicity was mediated by 4F2+, T8−, HNK-1− activated E+ cells. After 10 days in culture, killing of autologous lclebv increased continuously, from 4 ± 3% at Day 10 to 38 ± 4% by Day 22. The cytotoxicity to lclebv was mediated by classical T8+ CTL, and it was antigen specific and at least partially HLA Class I restricted. The regression of BEBV growth that occurs in e+/bebv cocultures coincides with the development of this CTL-mediated cytotoxicity.