Abstract
Virus-specific memory T cell populations demonstrate plasticity in antigen recognition and in their ability to accommodate new memory T cell populations. The degeneracy of T cell antigen recognition and the flexibility of diverse antigen-specific repertoires allow the host to respond to a multitude of pathogens while accommodating these numerous large memory pools in a finite immune system. These cross-reactive memory T cells can be employed in immune responses and mediate protective immunity, but they can also induce life-threatening immunopathology or impede transplantation tolerance and graft survival. Here we discuss examples of altered viral pathogenesis occurring as a consequence of heterologous T cell immunity and propose models for the maintenance of a dynamic pool of memory cells.
Original language | English (US) |
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Pages (from-to) | 335-347 |
Number of pages | 13 |
Journal | Seminars in Immunology |
Volume | 16 |
Issue number | 5 |
DOIs | |
State | Published - Oct 2004 |
Externally published | Yes |
Keywords
- Allo-reactive
- Cross-reactive
- Heterologous immunity
- Memory T cell
- Memory attrition
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology