His primary areas of study are T-cell receptor, Epitope, CD8, Antigen and T cell. His T-cell receptor study integrates concerns from other disciplines, such as Molecular biology, Biophysics and MHC class I, Major histocompatibility complex. The concepts of his Epitope study are interwoven with issues in Human leukocyte antigen, CTL* and Avidity.
His CTL* research includes themes of Tetramer and Virology. His work in Antigen addresses subjects such as Receptor, which are connected to disciplines such as Transplantation and Phage display. His work on CD28 as part of general T cell study is frequently connected to Dasatinib, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Andrew K. Sewell mainly focuses on T-cell receptor, T cell, Antigen, CD8 and Immunology. The T-cell receptor study combines topics in areas such as Molecular biology, Receptor, Cell biology, Epitope and Major histocompatibility complex. His T cell research is multidisciplinary, incorporating elements of Cancer research, Antibody and Flow cytometry.
His research in Antigen intersects with topics in Computational biology and Immunotherapy. His CD8 research is multidisciplinary, incorporating perspectives in Tetramer, Avidity and Effector. He interconnects Cancer and Type 1 diabetes in the investigation of issues within Immunology.
Andrew K. Sewell mostly deals with T-cell receptor, T cell, Antigen, Epitope and Immune system. The various areas that Andrew K. Sewell examines in his T-cell receptor study include Human leukocyte antigen, Cancer immunotherapy, Peptide and Cell biology. His T cell research integrates issues from Cancer research, MHC class I, CD8, Virus and Antibody.
The study incorporates disciplines such as Effector and Virology in addition to CD8. His research in the fields of Major histocompatibility complex overlaps with other disciplines such as Context. His Epitope study combines topics in areas such as Molecular biology, Influenza A virus, Antigen presentation and Immunogenicity.
Andrew K. Sewell spends much of his time researching T-cell receptor, T cell, Antigen, Epitope and Major histocompatibility complex. His studies in T-cell receptor integrate themes in fields like Complementarity determining region and Sequence analysis. His T cell research includes elements of MHC class I and CD8.
His research integrates issues of T-Cell Antigen Receptor Specificity, Virology, Immunodominance and Cell biology in his study of CD8. His studies deal with areas such as Receptor, Computational biology and Molecular Sequence Annotation as well as Antigen. Andrew K. Sewell has included themes like Combinatorial chemistry, Synthetic biology and Immunogenicity in his Epitope study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
POSITIVE SELECTION OF HIV-1 CYTOTOXIC T LYMPHOCYTE ESCAPE VARIANTS DURING PRIMARY INFECTION
David A. Price;Philip J. R. Goulder;Paul Klenerman;Andrew K. Sewell.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Monoclonal TCR-redirected tumor cell killing
Nathaniel Liddy;Giovanna Bossi;Katherine J. Adams;Anna Lissina.
Nature Medicine (2012)
Early highly active antiretroviral therapy for acute HIV-1 infection preserves immune function of CD8+ and CD4+ T lymphocytes
Annette Oxenius;David A. Price;Philippa J. Easterbrook;Christopher A. O'Callaghan.
Proceedings of the National Academy of Sciences of the United States of America (2000)
Avidity for antigen shapes clonal dominance in CD8 + T cell populations specific for persistent DNA viruses
David A. Price;Jason M. Brenchley;Laura E. Ruff;Michael R. Betts.
Journal of Experimental Medicine (2005)
CTLs are targeted to kill β cells in patients with type 1 diabetes through recognition of a glucose-regulated preproinsulin epitope
Ania Skowera;Richard J. Ellis;Ruben Varela-Calviño;Sefina Arif.
Journal of Clinical Investigation (2008)
A Single Autoimmune T Cell Receptor Recognizes More Than a Million Different Peptides
Linda Wooldridge;Julia Ekeruche-Makinde;Hugo A. van den Berg;Anna Skowera;Anna Skowera.
Journal of Biological Chemistry (2012)
Why must T cells be cross-reactive?
Andrew K. Sewell.
Nature Reviews Immunology (2012)
The Bisphosphonate Acute Phase Response: Rapid and Copious Production of Proinflammatory Cytokines by Peripheral Blood Gd T Cells in Response to Aminobisphosphonates Is Inhibited by Statins
R. E. Hewitt;A. Lissina;A. E. Green;E. S. Slay.
Clinical and Experimental Immunology (2005)
Patterns of immunodominance in HIV-1-specific cytotoxic T lymphocyte responses in two human histocompatibility leukocyte antigens (HLA)-identical siblings with HLA-A*0201 are influenced by epitope mutation
P.J.R. Goulder;A.K. Sewell;D.G. Lalloo;David Price.
Journal of Experimental Medicine (1997)
Transmission and accumulation of CTL escape variants drive negative associations between HIV polymorphisms and HLA
Alasdair Leslie;Daniel Kavanagh;Isobella Honeyborne;Katja Pfafferott.
Journal of Experimental Medicine (2005)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Aberdeen
James Cook University
Continuum Life Sciences
Cardiff University
King's College London
University of Oxford
University of Oxford
Monash University
University of Oxford
Chinese Center For Disease Control and Prevention
Yale University
KU Leuven
Graz University of Technology
Technical University of Munich
National Academies of Sciences, Engineering, and Medicine
University of Paris-Saclay
University Medical Center Groningen
University of California, Berkeley
University of Arizona
Agriculture and Agriculture-Food Canada
Peking University
Purdue University West Lafayette
St George's, University of London
Peking University
National Oceanic and Atmospheric Administration
University of Illinois at Chicago