Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single b cells

This thesis outlines the development of the very first technology for high-throughput analysis of paired heavy and light-chain antibody sequences, opening the door for the discovery of new antibodies and the investigation of adaptive immune responses to vaccines and diseases. By designing two new te...

Full description

Saved in:
Bibliographic Details
Main Author DeKosky, Brandon (Author)
Format Electronic eBook
LanguageEnglish
Published Cham : Springer, 2017.
SeriesSpringer theses.
Subjects
Online AccessFull text
ISBN9783319585185
9783319585178
Physical Description1 online resource

Cover

Table of Contents:
  • Supervisor's Foreword; Preface; Parts of this thesis have been published in the following journal articles:DeKosky, B.J., Ippolito, G.C., Deschner, R.P., Lavinder, J.J., Wine, Y., Rawlings, B.M., Varadarajan, N., Giesecke, C., Dorner, T., Andrews, S.F., Wilson, P.C., Hunicke-Smith, S.P., Willson, C.G., Ellington, A.D. & Georgiou, G. High-throughput sequencing of the paired human immunoglobulin heavy and light chain repertoire. Nature Biotechnology 31, 166-169 (2013). DeKosky, B.J., Kojima, T., Rodin, A., Charab, W., ; Acknowledgements; Contents; Abbreviations; List of Figures.
  • List of Tables1 Background; 1.1 Antibodies and Antibody Repertoire Development; 1.2 Adaptive Immune Responses Lead to B-Cell Activation and Antibody Secretion; 1.3 High Throughput Antibody Sequencing; 1.4 Next Generation Antibody Sequencing Data Analysis; 1.5 Monoclonal Antibody Discovery Technologies; 1.6 Single-Cell Sequencing Techniques; 1.7 Synopsis; References; 2 High-Throughput Sequencing of the Paired Human Immunoglobulin Heavy and Light Chain Repertoire; 2.1 Rationale and Supporting Information; 2.2 Methodology; 2.3 Results; 2.4 Discussion; 2.5 Methods; References.
  • 3 In-Depth Determination and Analysis of the Human Paired Heavy and Light Chain Antibody Repertoire3.1 Introduction; 3.2 Results; 3.2.1 Device Construction; 3.2.2 Single B Cell VH:VL Pairing: Throughput and Pairing Accuracy; 3.2.3 Promiscuous and Public VL Junctions; 3.2.4 Quantifying Allelic Inclusion in Human Memory B Cells; 3.2.5 Antibodies with Gene Signatures of Known Anti-Viral BNAbs; 3.3 Discussion; 3.4 Methods; References; 4 Paired VH:VL Analysis of Naïve B Cell Repertoires and Comparison to Antigen-Experienced B Cell Repertoires in Healthy Human Donors; 4.1 Introduction; 4.2 Results.
  • 4.2.1 VH:VL Gene Usage Across B Cell Subsets4.2.2 CDR3 Length Analysis; 4.2.3 CDR3 Charge; 4.2.4 CDR3 Hydrophobicity; 4.2.5 Public Heavy and Light Chain Sequences; 4.3 Discussion; 4.4 Methods; 4.4.1 Ethics Statement; 4.4.2 Cell Isolation and VH:VL Pairing; 4.4.3 Bioinformatic Analysis; 4.4.4 Statistical Analysis; References; 5 Conclusions and Future Perspectives; References; Appendix A: Chapter 2 Supplementary Information; Appendix A: Chapter 2 Supplementary Information; Appendix B: Chapter 3 Supplementary Information; Appendix C: Chapter 4 Supplementary Information; Index.