Maintenance of the EBV-specific CD8+ TCRαβ repertoire in immunosuppressed lung transplant recipients
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Title
Maintenance of the EBV-specific CD8+
TCRαβ repertoire in immunosuppressed lung transplant recipients
Authors
Keywords
-
Journal
IMMUNOLOGY AND CELL BIOLOGY
Volume 95, Issue 1, Pages 77-86
Publisher
Wiley
Online
2016-08-10
DOI
10.1038/icb.2016.71
References
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Related references
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- Understanding the complexity and malleability of T-cell recognition
- (2015) John J Miles et al. IMMUNOLOGY AND CELL BIOLOGY
- Misinitiation of intrathymicMART-1transcription and biased TCR usage explain the high frequency of MART-1-specific T cells
- (2014) Sheena Pinto et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- TCR -Chain Sharing in Human CD8+ T Cell Responses to Cytomegalovirus and EBV
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- Preexisting CD8+ T-cell immunity to the H7N9 influenza A virus varies across ethnicities
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- Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
- (2013) Thi H. O. Nguyen et al. PLoS One
- CD8+ TCR Repertoire Formation Is Guided Primarily by the Peptide Component of the Antigenic Complex
- (2012) D. Koning et al. JOURNAL OF IMMUNOLOGY
- T Cell Receptor Diversity Inversely Correlates with Pathogen-Specific Antibody Levels in Human Cytomegalovirus Infection
- (2012) G. C. Wang et al. Science Translational Medicine
- Bias in the αβ T-cell repertoire: implications for disease pathogenesis and vaccination
- (2011) John J Miles et al. IMMUNOLOGY AND CELL BIOLOGY
- Primary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion
- (2010) Nicole L. La Gruta et al. JOURNAL OF CLINICAL INVESTIGATION
- Multiplexed combinatorial tetramer staining in a mouse model of virus infection
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- Cross-reactive CD8+T-cell immunity between the pandemic H1N1-2009 and H1N1-1918 influenza A viruses
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- Clonotype Selection and Composition of Human CD8 T Cells Specific for Persistent Herpes Viruses Varies with Differentiation but Is Stable Over Time
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- IMGT/V-QUEST: the highly customized and integrated system for IG and TR standardized V-J and V-D-J sequence analysis
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