Quantification of epitope abundance reveals the effect of direct and cross-presentation on influenza CTL responses
暂无分享,去创建一个
D. Tscharke | J. Sidney | A. Sette | N. Gruta | P. Thomas | A. Handel | N. Croft | A. Purcell | N. L. La Gruta | L. Wakim | Ting Wu | Jing Guan | Xavier Y. X. Sng | P. Thomas
[1] Trevor Hastie,et al. An Introduction to Statistical Learning , 2013, Springer Texts in Statistics.
[2] Sri H. Ramarathinam,et al. Mass spectrometry–based identification of MHC-bound peptides for immunopeptidomics , 2019, Nature Protocols.
[3] David F. Boyd,et al. Human CD8+ T cell cross-reactivity across influenza A, B and C viruses , 2019, Nature Immunology.
[4] Bjoern Peters,et al. Most viral peptides displayed by class I MHC on infected cells are immunogenic , 2019, Proceedings of the National Academy of Sciences.
[5] Martin Eisenacher,et al. The PRIDE database and related tools and resources in 2019: improving support for quantification data , 2018, Nucleic Acids Res..
[6] V. Warnault,et al. Signaling , 2018, Modeling Strategic Behavior.
[7] Sri H. Ramarathinam,et al. A subset of HLA-I peptides are not genomically templated: Evidence for cis- and trans-spliced peptide ligands , 2018, Science Immunology.
[8] Anthony W Purcell,et al. In Immunopeptidomics We Need a Sniper Instead of a Shotgun , 2018, Proteomics.
[9] Morten Nielsen,et al. Bioinformatics Tools for the Prediction of T-Cell Epitopes. , 2018, Methods in molecular biology.
[10] Sri H. Ramarathinam,et al. MHC-I peptides get out of the groove and enable a novel mechanism of HIV-1 escape , 2017, Nature Structural &Molecular Biology.
[11] M. Nielsen,et al. Unconventional Peptide Presentation by Major Histocompatibility Complex (MHC) Class I Allele HLA-A*02:01 , 2017, The Journal of Biological Chemistry.
[12] Kylie M. Quinn,et al. Reversed T Cell Receptor Docking on a Major Histocompatibility Class I Complex Limits Involvement in the Immune Response. , 2016, Immunity.
[13] Joseph C. Sun,et al. Epitope-Specific Vaccination Limits Clonal Expansion of Heterologous Naive T Cells during Viral Challenge. , 2016, Cell reports.
[14] Marco Y. Hein,et al. The Perseus computational platform for comprehensive analysis of (prote)omics data , 2016, Nature Methods.
[15] Bernd Bischl,et al. mlr: Machine Learning in R , 2016, J. Mach. Learn. Res..
[16] Bernd Bischl,et al. Machine Learning in R , 2015 .
[17] Nathan P Croft,et al. Quantifying epitope presentation using mass spectrometry. , 2015, Molecular immunology.
[18] D. Tscharke,et al. Sizing up the key determinants of the CD8+ T cell response , 2015, Nature Reviews Immunology.
[19] L. Saveanu,et al. Cross-Presentation of Cell-Associated Antigens by MHC Class I in Dendritic Cell Subsets , 2015, Front. Immunol..
[20] Elisa Pappalardo,et al. Early Kinetics of the HLA Class I-Associated Peptidome of MVA.HIVconsv-Infected Cells , 2015, Journal of Virology.
[21] U. Grömping. Variable importance in regression models , 2015 .
[22] Dmitri I. Kotov,et al. T cell receptor cross-reactivity between similar foreign and self peptides influences naive cell population size and autoimmunity. , 2015, Immunity.
[23] J. Drijfhout,et al. Naturally Processed Non-canonical HLA-A*02:01 Presented Peptides* , 2014, The Journal of Biological Chemistry.
[24] Weisan Chen,et al. Standard and immunoproteasomes show similar peptide degradation specificities , 2014, European journal of immunology.
[25] P. Kloetzel,et al. Proteasome isoforms exhibit only quantitative differences in cleavage and epitope generation , 2014, European journal of immunology.
[26] P. Doherty,et al. The Influenza Virus–Specific CTL Immunodominance Hierarchy in Mice Is Determined by the Relative Frequency of High-Avidity T Cells , 2014, The Journal of Immunology.
[27] Cheng Zhu,et al. Accumulation of Dynamic Catch Bonds between TCR and Agonist Peptide-MHC Triggers T Cell Signaling , 2014, Cell.
[28] Garnet Navarro,et al. Characterization of innate responses to influenza virus infection in a novel lung type I epithelial cell model. , 2014, The Journal of general virology.
[29] P. Doherty,et al. Reproducible selection of high avidity CD8+ T-cell clones following secondary acute virus infection , 2014, Proceedings of the National Academy of Sciences.
[30] James McCluskey,et al. HLA Peptide Length Preferences Control CD8+ T Cell Responses , 2013, The Journal of Immunology.
[31] J. Yewdell,et al. Mixed Proteasomes Function To Increase Viral Peptide Diversity and Broaden Antiviral CD8+ T Cell Responses , 2013, The Journal of Immunology.
[32] Clemencia Pinilla,et al. Measurement of MHC/Peptide Interactions by Gel Filtration or Monoclonal Antibody Capture , 2013, Current protocols in immunology.
[33] Anthony W. Purcell,et al. Kinetics of Antigen Expression and Epitope Presentation during Virus Infection , 2013, PLoS pathogens.
[34] K. Pang,et al. Increasing Viral Dose Causes a Reversal in CD8+ T Cell Immunodominance during Primary Influenza Infection due to Differences in Antigen Presentation, T Cell Avidity, and Precursor Numbers , 2013, The Journal of Immunology.
[35] A. Moosmann,et al. Mature proteins derived from Epstein–Barr virus fail to feed into the MHC class I antigenic pool , 2012, European journal of immunology.
[36] Morten Nielsen,et al. Peptide‐MHC class I stability is a better predictor than peptide affinity of CTL immunogenicity , 2012, European journal of immunology.
[37] Philip E. Bourne,et al. Immune epitope database analysis resource , 2012, Nucleic Acids Res..
[38] R. Fåhraeus,et al. Major source of antigenic peptides for the MHC class I pathway is produced during the pioneer round of mRNA translation , 2011, Proceedings of the National Academy of Sciences.
[39] P. Doherty,et al. Primary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion. , 2010, The Journal of clinical investigation.
[40] Brendan MacLean,et al. Bioinformatics Applications Note Gene Expression Skyline: an Open Source Document Editor for Creating and Analyzing Targeted Proteomics Experiments , 2022 .
[41] J. Yewdell,et al. Defective Ribosomal Products Are the Major Source of Antigenic Peptides Endogenously Generated from Influenza A Virus Neuraminidase , 2009, The Journal of Immunology.
[42] Keiji Tanaka,et al. Critical role for the immunoproteasome subunit LMP7 in the resistance of mice to Toxoplasma gondii infection , 2009, European Journal of Immunology.
[43] M. Mann,et al. Universal sample preparation method for proteome analysis , 2009, Nature Methods.
[44] M. Mann,et al. MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification , 2008, Nature Biotechnology.
[45] Bjoern Peters,et al. Naive Precursor Frequencies and MHC Binding Rather Than the Degree of Epitope Diversity Shape CD8+ T Cell Immunodominance1 , 2008, The Journal of Immunology.
[46] Clare L. Bennett,et al. Clearance of influenza virus from the lung depends on migratory langerin+CD11b− but not plasmacytoid dendritic cells , 2008, The Journal of experimental medicine.
[47] J. Yewdell,et al. The exception that reinforces the rule: crosspriming by cytosolic peptides that escape degradation. , 2008, Immunity.
[48] L. Otten,et al. In vivo transformation of mouse conventional CD8alpha+ dendritic cells leads to progressive multisystem histiocytosis. , 2008, Blood.
[49] Bjoern Peters,et al. A Quantitative Analysis of the Variables Affecting the Repertoire of T Cell Specificities Recognized after Vaccinia Virus Infection1 , 2007, The Journal of Immunology.
[50] Scott A. Brown,et al. Hidden Epitopes Emerge in Secondary Influenza Virus-Specific CD8+ T Cell Reponses1 , 2007, The Journal of Immunology.
[51] Nicholas A Williamson,et al. A T cell receptor flattens a bulged antigenic peptide presented by a major histocompatibility complex class I molecule , 2007, Nature Immunology.
[52] R. Webby,et al. Addition of a Prominent Epitope Affects Influenza A Virus-Specific CD8+ T Cell Immunodominance Hierarchies When Antigen Is Limiting1 , 2006, The Journal of Immunology.
[53] Ulrike Groemping,et al. Relative Importance for Linear Regression in R: The Package relaimpo , 2006 .
[54] Magdalini Moutaftsi,et al. A consensus epitope prediction approach identifies the breadth of murine TCD8+-cell responses to vaccinia virus , 2006, Nature Biotechnology.
[55] R. Webby,et al. A virus-specific CD8+ T cell immunodominance hierarchy determined by antigen dose and precursor frequencies. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[56] Eric W. Deutsch,et al. The PeptideAtlas project , 2005, Nucleic Acids Res..
[57] N. Brouwenstijn,et al. Antigen Bias in T Cell Cross-Priming , 2004, Science.
[58] D. Tscharke,et al. CD8+ T Cell Cross-Priming via Transfer of Proteasome Substrates , 2004, Science.
[59] Ellis L Reinherz,et al. Genome-wide Characterization of a Viral Cytotoxic T Lymphocyte Epitope Repertoire* , 2003, Journal of Biological Chemistry.
[60] H. Rammensee,et al. Discrete Cleavage Motifs of Constitutive and Immunoproteasomes Revealed by Quantitative Analysis of Cleavage Products , 2001, The Journal of experimental medicine.
[61] P. Doherty,et al. Diversity of Epitope and Cytokine Profiles for Primary and Secondary Influenza A Virus-Specific CD8+ T Cell Responses1 , 2001, The Journal of Immunology.
[62] J. Altman,et al. A Previously Unrecognized H-2Db-Restricted Peptide Prominent in the Primary Influenza A Virus-Specific CD8+T-Cell Response Is Much Less Apparent following Secondary Challenge , 2000, Journal of Virology.
[63] A. Rickinson,et al. HLA-B27 subtype polymorphism and CTL epitope choice: studies with EBV peptides link immunogenicity with stability of the B27:peptide complex. , 1998, Journal of immunology.
[64] Rolf M. Zinkernagel,et al. Original antigenic sin impairs cytotoxic T lymphocyte responses to viruses bearing variant epitopes , 1998, Nature.
[65] Eric G. Pamer,et al. Evolution of a Complex T Cell Receptor Repertoire during Primary and Recall Bacterial Infection , 1998, The Journal of experimental medicine.
[66] K. Wiesmüller,et al. Peptide length preferences for rat and mouse MHC class I molecules using random peptide libraries , 1998, European journal of immunology.
[67] A Sette,et al. Two complementary methods for predicting peptides binding major histocompatibility complex molecules. , 1997, Journal of molecular biology.
[68] K. Rock,et al. Cloned dendritic cells can present exogenous antigens on both MHC class I and class II molecules. , 1997, Journal of immunology.
[69] A. Vitiello,et al. Immunodominance analysis of CTL responses to influenza PR8 virus reveals two new dominant and subdominant Kb-restricted epitopes. , 1996, Journal of immunology.
[70] A. Vitiello,et al. The relationship between class I binding affinity and immunogenicity of potential cytotoxic T cell epitopes. , 1994, Journal of immunology.
[71] A. Goldberg,et al. Peptidase activities of proteasomes are differentially regulated by the major histocompatibility complex-encoded genes for LMP2 and LMP7. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[72] K. Kosmatopoulos,et al. A nonimmunodominant nucleoprotein-derived peptide is presented by influenza A virus-infected H-2b cells. , 1994, Journal of immunology.
[73] D. Finley,et al. MHC-linked LMP gene products specifically alter peptidase activities of the proteasome , 1993, Nature.
[74] M. Bevan,et al. Introduction of soluble protein into the class I pathway of antigen processing and presentation , 1988, Cell.
[75] A. McMichael,et al. The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides , 1986, Cell.