Abstract
Homeostatic mechanism by which peripheral T-cell subsets are maintained in vivo remains largely unknown. Using a T-cell proliferation model under lymphopenic settings, we now demonstrate that γδ T cells limit CD8 T-cell expansion but not the initial proliferation after transfer into lymphopenic recipients. Interleukin-15 (IL-15) produced by and transpresented on the membrane of the CD11c+ dendritic cells (DCs) is the key factor that mediates homeostatic competition between CD8 and γδ T cells, revealing previously unrecognized IL-15-dependent homeostatic mechanisms between different T-cell subsets in vivo.
Original language | English (US) |
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Pages (from-to) | 6361-6371 |
Number of pages | 11 |
Journal | Blood |
Volume | 113 |
Issue number | 25 |
DOIs | |
State | Published - 2009 |
Externally published | Yes |
Funding
ASJC Scopus subject areas
- Hematology
- Biochemistry
- Cell Biology
- Immunology