Abstract
During an infection, T cells can differentiate into multiple types of effector and memory T cells, which help to mediate pathogen clearance and provide long-term protective immunity. These cells can vary in their phenotype, function and location, and in their long-term fate in terms of their ability to populate the memory T cell pool. Over the past decade, the signalling pathways and transcriptional programmes that regulate the formation of heterogeneous populations of effector and memory CD8+ T cells have started to be characterized, and this Review discusses the major advances in these areas.
Original language | English (US) |
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Pages (from-to) | 749-761 |
Number of pages | 13 |
Journal | Nature Reviews Immunology |
Volume | 12 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2012 |
Funding
We thank the members of the Kaech laboratory for helpful com‑ ments and discussions. This work was supported by grants to S.M.K. from the US National Institutes of Health (grants R01AI074699, RO1AI066232, R21AI097767 and R21AI081150) and from the Howard Hughes Medical Institute.
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology