Polyomavirus-Infected Dendritic Cells Induce Antiviral CD8 + T Lymphocytes

Author:

Drake Donald R.1,Moser Janice M.1,Hadley Annette1,Altman John D.23,Maliszewski Charles4,Butz Eric4,Lukacher Aron E.1

Affiliation:

1. Department of Pathology,1

2. Department of Microbiology and Immunology,2 and the

3. Emory Vaccine Center,3 Emory University School of Medicine, Atlanta, Georgia 30322, and

4. Immunex Corporation, Seattle, Washington 981014

Abstract

ABSTRACT CD8 + T cells are critical for the clearance of acute polyomavirus infection and the prevention of polyomavirus-induced tumors, but the antigen-presenting cell(s) involved in generating polyomavirus-specific CD8 + T cells have not been defined. We investigated whether dendritic cells and macrophages are permissive for polyomavirus infection and examined their potential for inducing antiviral CD8 + T cells. Although dendritic cells and macrophages both supported productive polyomavirus infection, dendritic cells were markedly more efficient at presenting the immunodominant viral epitope to CD8 + T cells. Additionally, infected dendritic cells, but not infected macrophages, primed anti-polyomavirus CD8 + T cells in vivo. Treatment with Flt3 ligand, a hematopoietic growth factor that dramatically expands the number of dendritic cells, markedly enhanced the magnitude of virus-specific CD8 + T-cell responses during acute infection and the pool of memory anti-polyomavirus CD8 + T cells. These findings suggest that virus-infected dendritic cells induce polyomavirus-specific CD8 + T cells in vivo and raise the potential for their use as cellular adjuvants to promote CD8 + T cell surveillance against polyomavirus-induced tumors.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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