Rapid Effector Function in CD8+ Memory T Cells

TLDR

The nature of the CD8⁺ T cells that underlie antiviral protective immunological memory in vivo is unclear. We characterized peptide‑specific CD8⁺ T lymphocytes directly ex vivo from peripheral blood in humans with past influenza exposure, measuring single‑cell IFN‑γ release as an effector function assay. In memory individuals, antigen‑specific CD8⁺ T cells released IFN‑γ within 6 h of antigen contact, indicating a rapid effector population that can be quantified at frequencies severalfold higher than CTL precursors and persists long after infection, suggesting a role in protective memory.

Abstract

The nature of the CD8+ T cells that underlie antiviral protective immunological memory in vivo is unclear. We have characterized peptide-specific CD8+ T lymphocytes directly ex vivo from peripheral blood in humans with past exposure to influenza virus, using single cell interferon γ (IFN-γ) release as a measure of effector function. In individuals in the memory state with respect to influenza virus infection, unrestimulated antigen-specific CD8+ T cells displayed IFN-γ release within 6 h of antigen contact, identifying a population of memory CD8+ T cells that exhibit effector function without needing to divide and differentiate over several days. We have quantified circulating CD8+ effector T cells specific for six different MHC class I–restricted influenza virus epitopes. Enumeration of these CD8+ T cells gives frequencies of peptide-specific T cells that correlate with, but are in general severalfold higher than, CTL precursor frequencies derived from limiting dilution analysis, indicating that this novel population of memory CD8+ T cells has hitherto been undetected by standard means. The phenotype of these cells, which persist at a low frequency long after recovery from an acute viral infection, suggests that they play a role in protective immunological memory.