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CXCR3 Identifies Human Naive CD8+ T Cells with Enhanced Effector Differentiation Potential
G. De Simone, EMC. Mazza, A. Cassotta, AN. Davydov, M. Kuka, V. Zanon, F. De Paoli, E. Scamardella, M. Metsger, A. Roberto, K. Pilipow, FS. Colombo, E. Tenedini, E. Tagliafico, L. Gattinoni, D. Mavilio, C. Peano, DA. Price, SP. Singh, JM. Farber,...
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Intramural, práce podpořená grantem
Grantová podpora
100326/Z/12/Z
Wellcome Trust - United Kingdom
NLK
Free Medical Journals
od 1998 do Před 1 rokem
Freely Accessible Science Journals
od 1998-01-01 do Před 1 rokem
Open Access Digital Library
od 1998-01-01
PubMed
31740485
DOI
10.4049/jimmunol.1901072
Knihovny.cz E-zdroje
- MeSH
- aktivace lymfocytů imunologie MeSH
- biologické markery MeSH
- buněčná diferenciace imunologie MeSH
- CD8-pozitivní T-lymfocyty imunologie metabolismus MeSH
- dospělí MeSH
- imunofenotypizace MeSH
- imunologická paměť MeSH
- kultivované buňky MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- myši MeSH
- receptory CXCR3 metabolismus MeSH
- senioři MeSH
- T-lymfocyty - podskupiny imunologie metabolismus MeSH
- věkové faktory MeSH
- zvířata MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- myši MeSH
- senioři MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Intramural MeSH
In mice, the ability of naive T (TN) cells to mount an effector response correlates with TCR sensitivity for self-derived Ags, which can be quantified indirectly by measuring surface expression levels of CD5. Equivalent findings have not been reported previously in humans. We identified two discrete subsets of human CD8+ TN cells, defined by the absence or presence of the chemokine receptor CXCR3. The more abundant CXCR3+ TN cell subset displayed an effector-like transcriptional profile and expressed TCRs with physicochemical characteristics indicative of enhanced interactions with peptide-HLA class I Ags. Moreover, CXCR3+ TN cells frequently produced IL-2 and TNF in response to nonspecific activation directly ex vivo and differentiated readily into Ag-specific effector cells in vitro. Comparative analyses further revealed that human CXCR3+ TN cells were transcriptionally equivalent to murine CXCR3+ TN cells, which expressed high levels of CD5. These findings provide support for the notion that effector differentiation is shaped by heterogeneity in the preimmune repertoire of human CD8+ T cells.
Central European Institute of Technology 621 00 Brno Czech Republic
Department of Life Sciences University of Modena and Reggio Emilia 41125 Modena Italy
Humanitas Flow Cytometry Core Humanitas Clinical and Research Center 20089 Rozzano Milan Italy
IFOM FIRC Institute of Molecular Oncology 20139 Milan Italy
IRGB National Research Council 09042 Monserrato Italy
Pirogov Russian National Research Medical University 117997 Moscow Russia
Citace poskytuje Crossref.org
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