A long-standing paradox in cellular immunology concerns the conditional requirement for CD4 + T-helper (T H ) cells in the priming of cytotoxic CD8 + T lymphocyte (CTL) responses in vivo . Whereas CTL responses against certain viruses can be primed in the absence of CD4 + T cells, others, such as those mediated through ‘cross-priming’ by host antigen-presenting cells, are dependent on T H cells 1 , 2 , 3 , 4 . A clearer understanding of the contribution of T H cells to CTL development has been hampered by the fact that most T H -independent responses have been demonstrated ex vivo as primary cytotoxic effectors, whereas T H -dependent responses generally require secondary in vitro re-stimulation for their detection. Here, we have monitored the primary and secondary responses of T H -dependent and T H -independent CTLs and find in both cases that CD4 + T cells are dispensable for primary expansion of CD8 + T cells and their differentiation into cytotoxic effectors. However, secondary CTL expansion (that is, a secondary response upon re-encounter with antigen) is wholly dependent on the presence of T H cells during, but not after, priming. Our results demonstrate that T-cell help is ‘programmed’ into CD8 + T cells during priming, conferring on these cells a hallmark of immune response memory: the capacity for functional expansion on re-encounter with antigen.
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Science,Humanities and Social Sciences,multidisciplinary