The role of IL-2 and T4+ cells in the generation of human influenza virus-specific CTL activity

Abstract Stimulation of human peripheral blood lymphocytes (PBL) with influenza A virus leads to the generation of virus-specific cytotoxic T lymphocyte (CTL) activity as well as natural killer (NK)-like activity. In this study, we show that exogenous IL-2 augments the in vitro generation of virusspecific CTL activity, only when added some days after the initiation of the culture. Apparently, the endogenously produced IL-2 can be a limiting factor in the in vitro generation of CTL activity. The increase of influenza virus-specific CTL activity after addition of exogenous IL-2 does not affect the restriction pattern of the CTL response. So, the preferential use of certain HLA antigens as restriction elements is not due to a limiting amount of endogenously produced IL-2. Depletion of T4 + cells completely abrogates the generation of virus-specific CTL activity. Addition of exogenous IL-2 to T4 + -cell-depleted cultures fully restores the generation of HLA-restricted virusspecific CTL activity. We conclude that in the in vitro generation of virus-specific CTL activity in bulk cultures of human PBL (1) the sole function of T4 + cells in human virus-specific CTL generation is the production of IL-2, (2) no cognitive cell interaction of T8 + CTL precursors with T4 + cells is required, and (3) in bulk cultures T8 + cells themselves are not able to produce sufficient amounts of IL-2 to ascertain the maturation of virus-specific CTL precursors into cytolytic T cells. Finally, we show that exogenous IL-2 also has a stimulatory effect on the NK-like or lymphokine-ctivated killer activity, which is always concomitantly induced in virus-specific CTL generation cultures, but has no influence on the levels of IFN produced in such cultures.