Nature Communications · 2017 · 207 citations · 48 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityClinical ImmunologyImmunoregulationAdaptive Immune ResponsesAntiviral TherapyImmunological MemoryT Cell ActivationT Cell ExhaustionViral HepatitisAdaptive Immune MemoryAdaptive Immune Responses To Viral InfectionCellular Immune MemoryChronic Antigen StimulationChronic Viral HepatitisImmune Memory MaintenanceMemory T Cell SubsetsPhenotypic Differentiation
Abstract Differentiation and fate of virus-specific CD8 + T cells after cessation of chronic antigen stimulation is unclear. Here we show that a TCF1 + CD127 + PD1 + hepatitis C virus (HCV)-specific CD8 + T-cell subset exists in chronically infected patients with phenotypic features of T-cell exhaustion and memory, both before and after treatment with direct acting antiviral (DAA) agents. This subset is maintained during, and for a long duration after, HCV elimination. After antigen re-challenge the less differentiated TCF1 + CD127 + PD1 + population expands, which is accompanied by emergence of terminally exhausted TCF1-CD127-PD1 hi HCV-specific CD8 + T cells. These results suggest the TCF1 + CD127 + PD1 + HCV-specific CD8 + T-cell subset has memory-like characteristics, including antigen-independent survival and recall proliferation. We thus provide evidence for the establishment of memory-like virus-specific CD8 + T cells in a clinically relevant setting of chronic viral infection and we uncover their fate after cessation of chronic antigen stimulation, implicating a potential strategy for antiviral immunotherapy.
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