J
Joseph G. Joyce
Researcher at Merck & Co.
Publications - 78
Citations - 5676
Joseph G. Joyce is an academic researcher from Merck & Co.. The author has contributed to research in topics: Antibody & Epitope. The author has an hindex of 31, co-authored 77 publications receiving 5510 citations. Previous affiliations of Joseph G. Joyce include United States Military Academy & Columbia University.
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Journal ArticleDOI
Replication-incompetent adenoviral vaccine vector elicits effective anti-immunodeficiency-virus immunity.
John W. Shiver,Tong-Ming Fu,Ling Chen,Danilo R. Casimiro,Mary-Ellen Davies,Robert K. Evans,Zhiqiang Zhang,Adam J. Simon,Wendy L. Trigona,Sheri Dubey,Lingyi Huang,Virginia Harris,Romnie Long,Xiaoping Liang,Larry Handt,William A. Schleif,Lan Zhu,Daniel C. Freed,Natasha Persaud,Liming Guan,Kara Punt,Aimin Tang,Minchun Chen,Keith A. Wilson,Kelly B. Collins,Gwendolyn J. Heidecker,V. Rose Fernandez,Helen C. Perry,Joseph G. Joyce,Karen M. Grimm,James C. Cook,Paul M. Keller,Denise S. Kresock,Henryk Mach,Robert D. Troutman,Lynne Isopi,Donna M. Williams,Zheng Xu,Kathryn E. Bohannon,David B. Volkin,David C. Montefiori,Ayako Miura,Georgia R. Krivulka,Michelle A. Lifton,Marcelo J. Kuroda,Jörn E. Schmitz,Norman L. Letvin,Michael J. Caulfield,Andrew J. Bett,Rima Youil,David C. Kaslow,Emilio A. Emini +51 more
TL;DR: The replication-defective adenovirus is a promising vaccine vector for development of an HIV-1 vaccine and elicited by a replication-incompetent Ad5 vector, used either alone or as a booster inoculation after priming with a DNA vector.
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The L1 major capsid protein of human papillomavirus type 11 recombinant virus-like particles interacts with heparin and cell-surface glycosaminoglycans on human keratinocytes
Joseph G. Joyce,Jwu-Sheng Tung,Craig T. Przysiecki,James C. Cook,E. Dale Lehman,Jeffrey A. Sands,Kathrin U. Jansen,Paul M. Keller +7 more
TL;DR: It is established for the first time that the carboxyl-terminal portion of HPV L1 interacts with heparin, and that this region appears to be crucial for interaction with the cell surface.
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Preclinical study of influenza virus A M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys
Jiang Fan,Xiaoping Liang,Melanie Horton,Helen C. Perry,Michael P. Citron,Gwen J Heidecker,Tong-Ming Fu,Joseph G. Joyce,Craig T. Przysiecki,Paul M. Keller,Victor M. Garsky,Roxana Ionescu,Yvette Rippeon,Li Shi,Michael Chastain,Jon H. Condra,Mary-Ellen Davies,Jason J. Z. Liao,Emilio A. Emini,John W. Shiver +19 more
TL;DR: Systematic evaluation of M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys revealed protection against lethal challenge of either H1N1 or H3N1 virus in mice and the ability to reduce viral shedding in the lower respiratory tracts of mice and ferrets.
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Immunochemical properties of the staphylococcal poly-N-acetylglucosamine surface polysaccharide
Tomas Maira-Litran,Andrea Kropec,C. Abeygunawardana,Joseph G. Joyce,George E. Mark,Donald A. Goldmann,Gerald B. Pier +6 more
TL;DR: The chemical structure of PS/A is determined to be β(1-6)-N-acetylglucosamine (PNAG), which helps to differentiate it from PIA on the basis of immunogenicity, molecular size, and solubility.
Journal ArticleDOI
A Novel Staphylococcus aureus Vaccine: Iron Surface Determinant B Induces Rapid Antibody Responses in Rhesus Macaques and Specific Increased Survival in a Murine S. aureus Sepsis Model
Nelly A. Kuklin,Desmond J. Clark,Susan Secore,Cook James C,Leslie Cope,Tessie McNeely,Liliane Noble,Martha Brown,Julie K. Zorman,Xin Min Wang,Gregory D. Pancari,Hongxia Fan,Kevin Isett,Bruce Burgess,Janine T. Bryan,Brownlow Michelle K,George Hugh A,Maria S. Meinz,Mary E. Liddell,Rosemarie Kelly,Schultz Loren D,Donna L. Montgomery,Janet C. Onishi,Maria C Losada,Melissa M. Martin,Timothy D Ebert,Charles Y. Tan,Timothy L. Schofield,Eszter Nagy,Andreas Meineke,Joseph G. Joyce,Myra B. Kurtz,Michael J. Caulfield,Kathrin U. Jansen,William L. Mcclements,Annaliesa S. Anderson +35 more
TL;DR: IsdB has excellent prospects for use as a vaccine against S. aureus disease in humans and was highly immunogenic in mice when it was formulated with amorphous aluminum hydroxyphosphate sulfate adjuvant, and the resulting antibody responses were associated with reproducible and significant protection in animal models of infection.