Abstract
CD8+ T cells are critical for protecting the body from infectious disease. To achieve this protection, CD8+ T cells must undergo a highly involved process of differentiation that involves the activation of näve/quiescent cells followed by robust rounds of cell division and the acquisition of effector functions that mediate viral clearance. After the pathogen is eliminated, a small number of these cells survive into long-lived memory and maintain the capacity to respond rapidly and reacquire effector function after secondary exposure to their cognate antigen. This review focuses on how CD8+ T cells acquire and regulate effector functions and how the capacity to produce effector molecules is maintained into memory.
| Original language | English |
|---|---|
| Pages (from-to) | 519-526 |
| Number of pages | 8 |
| Journal | IUBMB Life |
| Volume | 62 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 2010 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- CD8 T cells
- Cytokines
- Epigenetics; influenza
- Granzymes
- Perforin
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