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Current Immunology Reviews (Discontinued)

Editor-in-Chief

ISSN (Print): 1573-3955
ISSN (Online): 1875-631X

T Cell Memory Generation in the Face of Persistent Antigen Presentation

Author(s): Dawn M. Jelley-Gibbs and Susan L. Swain

Volume 3, Issue 4, 2007

Page: [240 - 250] Pages: 11

DOI: 10.2174/157339507783334183

Price: $65

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Abstract

In the face of emerging infectious diseases, we are challenged to develop innovative vaccine strategies that can protect against rapidly evolving and highly virulent pathogens. Since CD4 T cells are needed to generate and maintain protective B cell and CD8 T cell immunity, new vaccines should ideally elicit both T and B cell memory. In order to generate long-lived immune memory in both T and B cell compartments, such vaccines will need to induce cross-reactive memory against highly conserved antigens within a given pathogen. Acute influenza infection provides a model system whereby the generation of T cell memory is influenced by residual antigen depots. These antigen depots persist for months after live virus clearance, and provide continued, low level T cell stimulation. Here we discuss the impact and implications of residual pathogen-derived antigen depots on the generation and maintenance of T cell immunity. We propose that effective vaccines may need to include persistent depots of conserved proteins to generate a functionally flexible memory T cell pool that can confer protection against rapidly evolving pathogens.

Keywords: Antigen presentation, CD4 memory T cells, influenza, cognate help, vaccine, heterosubtypic immunity


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