Journal article
Cutting edge: differential self-peptide/MHC requirement for maintaining CD8 T cell function versus homeostatic proliferation
The Journal of immunology (1950), Vol.175(8), pp.4829-4833
10/15/2005
DOI: 10.4049/jimmunol.175.8.4829
PMID: 16210583
Abstract
Memory T cells do not require self-peptide/MHC (spMHC) complexes to survive long term in vivo. However, memory CD4 T cells lose the ability to reject skin grafts when transiently placed in an environment in which these low-level TCR stimulations are absent. Whether or not spMHC alters the ability of CD8 T cells to respond to stimulation in vivo remains unknown. Here, we show that memory CD8 T cells retain the ability to respond to dendritic cell-mediated stimulation after adoptive transfer into either TAP(-/-) (MHC class I-deficient) or wild-type mice. Surprisingly, naive CD8 T cells, which fail to undergo homeostatic proliferation and erode in number in the absence of MHC class I, also retain the ability to respond to dendritic cell-mediated antigenic stimulation for at least 1 wk after transfer into TAP(-/-) mice. These findings suggest a differential requirement for spMHC signals for maintenance of CD8 T cell function and homeostatic proliferation.
Details
- Title: Subtitle
- Cutting edge: differential self-peptide/MHC requirement for maintaining CD8 T cell function versus homeostatic proliferation
- Creators
- Ali Jabbari - Interdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, IA 52242, USAJohn T Harty
- Resource Type
- Journal article
- Publication Details
- The Journal of immunology (1950), Vol.175(8), pp.4829-4833
- DOI
- 10.4049/jimmunol.175.8.4829
- PMID
- 16210583
- NLM abbreviation
- J Immunol
- ISSN
- 0022-1767
- eISSN
- 1550-6606
- Publisher
- United States
- Grant note
- AI42767 / NIAID NIH HHS AI50073 / NIAID NIH HHS AI46653 / NIAID NIH HHS AI59752 / NIAID NIH HHS
- Language
- English
- Date published
- 10/15/2005
- Academic Unit
- Dermatology; Pathology
- Record Identifier
- 9984025445002771
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