T
Timothy Roach
Researcher at Queen Elizabeth II Hospital
Publications - 5
Citations - 1534
Timothy Roach is an academic researcher from Queen Elizabeth II Hospital. The author has contributed to research in topics: CTL* & Epitope. The author has an hindex of 5, co-authored 5 publications receiving 1499 citations.
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Journal ArticleDOI
HIV evolution: CTL escape mutation and reversion after transmission.
Alasdair Leslie,Katja Pfafferott,P Chetty,Rika Draenert,Marylyn M. Addo,Margaret E. Feeney,Yanhua Tang,Edward C. Holmes,Todd M. Allen,Julia G. Prado,Marcus Altfeld,Christian Brander,C Dixon,D Ramduth,P M Jeena,S A Thomas,A St John,Timothy Roach,Bernd Kupfer,Graz Luzzi,Adrian Edwards,Graham P. Taylor,Hermione Lyall,Gareth Tudor-Williams,Vas Novelli,Javier Martinez-Picado,Photini Kiepiela,Bruce D. Walker,Philip J. R. Goulder,Philip J. R. Goulder +29 more
TL;DR: Data show that the process of accumulation of escape mutations within HIV is not inevitable, and complex epitope- and residue-specific selection forces, including CTL-mediated positive selection pressure and virus-mediated purifying selection, operate in tandem to shape HIV evolution at the population level.
Journal ArticleDOI
Consistent Cytotoxic-T-Lymphocyte Targeting of Immunodominant Regions in Human Immunodeficiency Virus across Multiple Ethnicities
Nicole Frahm,Bette T. Korber,Bette T. Korber,C. M. Adams,James J. Szinger,Rika Draenert,Marylyn M. Addo,Margaret E. Feeney,Karina Yusim,Kaori Sango,Nancy V. Brown,Devi SenGupta,Alicja Piechocka-Trocha,T. Simonis,F. M. Marincola,Alysse G. Wurcel,David Stone,Christopher J. Russell,P. Adolf,Daniel E. Cohen,Timothy Roach,A. StJohn,Ashok Khatri,K. Davis,James I. Mullins,Philip J. R. Goulder,Bruce D. Walker,Christian Brander +27 more
TL;DR: Factors that contribute to the immunogenicity of these highly targeted and relatively conserved sequences in HIV that may represent promising vaccine candidates for ethnically heterogeneous populations are identified.
Journal ArticleDOI
Control of human immunodeficiency virus replication by cytotoxic T lymphocytes targeting subdominant epitopes.
Nicole Frahm,Photini Kiepiela,Sharon Adams,Caitlyn Linde,Hannah S. Hewitt,Kaori Sango,Margaret E. Feeney,Marylyn M. Addo,Mathias Lichterfeld,Matthew P. Lahaie,Eunice Pae,Alysse G. Wurcel,Alysse G. Wurcel,Timothy Roach,M. Anne St. John,Marcus Altfeld,Francesco M. Marincola,Corey Moore,Simon Mallal,Mary Carrington,David Heckerman,Todd M. Allen,James I. Mullins,Bette T. Korber,Bette T. Korber,Philip J. R. Goulder,Philip J. R. Goulder,Bruce D. Walker,Bruce D. Walker,Christian Brander +29 more
TL;DR: Analysis of cytotoxic T lymphocyte responses restricted by HLA-B*1503 suggests that subdominant responses can contribute to in vivo viral control and that high HLA allele frequencies may drive the elimination ofSubdominant yet effective epitopes from circulating viral populations.
Journal ArticleDOI
HLA-B63 Presents HLA-B57/B58-Restricted Cytotoxic T-Lymphocyte Epitopes and Is Associated with Low Human Immunodeficiency Virus Load
Nicole Frahm,Sharon Adams,Photini Kiepiela,Caitlyn Linde,Hannah S. Hewitt,Mathias Lichterfeld,Kaori Sango,Nancy V. Brown,Eunice Pae,Alysse G. Wurcel,Marcus Altfeld,Margaret E. Feeney,Todd M. Allen,Timothy Roach,M. Anne St. John,Eric S. Daar,Eric S. Rosenberg,Bette T. Korber,Francesco M. Marincola,Bruce D. Walker,Philip J. R. Goulder,Christian Brander +21 more
TL;DR: HLA-B63-positive subjects generated responses early in acute HIV infection and were able to control HIV replication in the absence of antiretroviral treatment and help to better define immune correlates of controlled HIV infection.
Journal ArticleDOI
Increased detection of HIV-specific T cell responses by combination of central sequences with comparable immunogenicity.
Nicole Frahm,David C. Nickle,Caitlyn Linde,Daniel E. Cohen,Rosario Zuñiga,Aldo Lucchetti,Timothy Roach,Bruce D. Walker,Todd M. Allen,Bette T. Korber,James I. Mullins,Christian Brander +11 more
TL;DR: All tested centralized antigens provided a similarly potent set of antigenic peptides, and the significantly broader responses detected using the combination of sets highlight the importance of maximizing coverage of HIV-1 sequence diversity in vaccine preparations, as well as in the evaluation of CTL responses in HIV- 1-infected individuals and those vaccinated.