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Neil C. Sheppard
Researcher at University of Oxford
Publications - 22
Citations - 759
Neil C. Sheppard is an academic researcher from University of Oxford. The author has contributed to research in topics: Immune system & Immunogenicity. The author has an hindex of 10, co-authored 17 publications receiving 685 citations. Previous affiliations of Neil C. Sheppard include Pfizer & GlaxoSmithKline.
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Journal ArticleDOI
Polyethyleneimine is a potent mucosal adjuvant for viral glycoprotein antigens.
Frank Wegmann,Kate H. Gartlan,Ali M. Harandi,Sarah A. Brinckmann,Margherita Coccia,William R. Hillson,Wai Ling Kok,S L Cole,Ling-Pei Ho,Teresa Lambe,Manoj Puthia,Catharina Svanborg,Erin M. Scherer,George Krashias,Adam Williams,Joseph N. Blattman,Philip D. Greenberg,Richard A. Flavell,Amin E. Moghaddam,Neil C. Sheppard,Neil C. Sheppard,Quentin J. Sattentau +21 more
TL;DR: Polyethyleneimine (PEI) represents a family of organic polycations used as nucleic acid transfection reagents in vitro and DNA vaccine delivery vehicles in vivo and it is shown that diverse PEI forms have potent mucosal adjuvant activity for viral subunit glycoprotein antigens.
Journal ArticleDOI
Expression-System-Dependent Modulation of HIV-1 Envelope Glycoprotein Antigenicity and Immunogenicity
Leopold Kong,Neil C. Sheppard,Guillaume Stewart-Jones,Cynthia L. Robson,Hongying Chen,Xiaodong Xu,George Krashias,Camille Bonomelli,Christopher N. Scanlan,Peter D. Kwong,Simon A. Jeffs,Ian M. Jones,Quentin J. Sattentau +12 more
TL;DR: It is suggested that non-sialic-acid-imparting systems yield gp120 immunogens with modified antigenic and immunogenic properties, considerations that should be considered when selecting expression systems for glycosylated antigens to be used for structure-function studies and for vaccine use.
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HERV-K–specific T cells eliminate diverse HIV-1/2 and SIV primary isolates
R. Brad Jones,Keith E. Garrison,Shariq Mujib,Vesna Mihajlovic,Nasra Aidarus,Diana V. Hunter,Eric Martin,Eric Martin,Vivek M. John,Wei Zhan,Nabil F. Faruk,Gabor Gyenes,Neil C. Sheppard,Ingrid M. Priumboom-Brees,David A. Goodwin,Lianchun Chen,Melanie Rieger,Sophie Muscat-King,Peter T. Loudon,Cole Stanley,Sara J. Holditch,Sara J. Holditch,Jessica Wong,Kiera L. Clayton,Erick Duan,Haihan Song,Yang Xu,Devi SenGupta,Ravi Tandon,Jonah B. Sacha,Mark A. Brockman,Erika Benko,Colin Kovacs,Douglas F. Nixon,Mario A. Ostrowski +34 more
TL;DR: This study establishes a rationale for eliminating HIV-1-infected cells by targeting cellular immune responses against stable human endogenous retroviral (HERV) antigens and identifies a second T cell response that exhibited cross-reactivity between homologous HIV- 1-Pol and HERV-K(HML-2)-Pol determinants, raising the possibility that homology between HIV-2 and HERVs plays a role in shaping, and perhaps enhancing, the T cellresponse to HIV
Journal ArticleDOI
EV01: a phase I trial in healthy HIV negative volunteers to evaluate a clade C HIV vaccine, NYVAC-C undertaken by the EuroVacc Consortium.
Pierre-Alexandre Bart,Ruth L. Goodall,Tristan Barber,Alexandre Harari,Ana Guimaraes-Walker,Mona Khonkarly,Neil C. Sheppard,Yolanda Bangala,Marie-Joelle Frachette,Ralf Wagner,Peter Liljeström,Jean-Pierre Kraehenbuhl,Marc Girard,Jaap Goudsmit,Mariano Esteban,Jonathan L. Heeney,Jonathan L. Heeney,Quentin J. Sattentau,Sheena McCormack,Abdel Babiker,Giuseppe Pantaleo,Jonathan Weber +21 more
TL;DR: NYVAC-C (vP2010), a recombinant vector expressing HIV subtype C gag, pol, env and nef antigens, was tested in a phase I study in healthy, HIV negative volunteers in London and Lausanne and found no serious adverse events, and no clinical or laboratory abnormalities or other events that led to withdrawal, interruption or dose reduction of the NYVAC/placebo.
Journal ArticleDOI
The trim5α genotype of rhesus macaques affects acquisition of simian immunodeficiency virus SIVsmE660 infection after repeated limiting-dose intrarectal challenge
Matthew R. Reynolds,Jonah B. Sacha,Jonah B. Sacha,Andrea M. Weiler,Gretta J. Borchardt,Chrystal E. Glidden,Neil C. Sheppard,Francesca A. Norante,Philip A. Castrovinci,Jacqueline J. Harris,Henry T. Robertson,Thomas C. Friedrich,Adrian B. McDermott,Nancy A. Wilson,David B. Allison,Wayne C. Koff,Welkin E. Johnson,David I. Watkins +17 more
TL;DR: The results indicate that the TRIM5 alleles can be a barrier to productive infection and that this should be taken into account when designing acquisition studies using SIVsmE660 or related viruses.