Proliferation and interleukin 5 production by CD8hiCD57+ T cells

Abstract

CD8^hiCD57⁺ T cells have previously been described as effector memory T cells with minimal expansion capacity and high susceptibility to activation‐induced cell death. In contrast, we demonstrate here that CD8^hiCD57⁺ T cells are capable of rapid expansion using multiple techniques including [³H]thymidine uptake, flow cytometric bead‐based enumeration and standard haemocytometer counting. Previous reports can be explained by marked inhibition of activation‐induced expansion and increased 7‐amino‐actinomycin D uptake by CD8^hiCD57⁺ T cells following treatment with CFSE, a dye previously used to measure their proliferation, combined with specific media requirements for the growth of this cell subset. The ability of CD8^hiCD57⁺ T cells to further differentiate is highlighted by a distinct cytokine profile late after activation that includes the unexpected release of high levels of interleukin 5. These data indicate that CD8^hiCD57⁺ T cells should not be considered as “end‐stage” effector T cells incapable of proliferation, but represent a highly differentiated subset capable of rapid division and exhibiting novel functions separate from their previously described cytotoxic and IFN‐γ responses.