Secondary Replicative Function of CD8 + T Cells That Had Developed an Effector Phenotype

Abstract

Models of the differentiation of memory CD8 + T cells that replicate during secondary infections differ over whether such cells had acquired effector function during primary infections. We created a transgenic mouse line that permits mapping of the fate of granzyme B (gzmB)–expressing CD8 + T cells and their progeny by indelibly marking them with enhanced yellow fluorescent protein (EYFP). Virus-specific CD8 + T cells express gzmB within the first 2 days of a primary response to infection with influenza, without impairment of continued primary clonal expansion. On secondary infection, virus-specific CD8 + T cells that became EYFP + during a primary infection clonally expand as well as all virus-specific CD8 + T cells. Thus, CD8 + T cells that have acquired an effector phenotype during primary infection may function as memory cells with replicative function.