Quadrivalent vaccine against human papillomavirus to prevent anogenital diseases.
By S. Garland, M. Hernández-Ávila, C. Wheeler, Gonzalo Pérez, D. Harper, S. Leodolter, G. W. Tang, D. Ferris, M. Steben, J. Bryan and 9 more. New England Journal of Medicine, 2007
2,030 citations recorded by the source corpus.
Subfields: Epidemiology, Immunology, Microbiology
View Paper: https://www.semanticscholar.org/paper/273e54f7d5ecd079566273fecf0d3f42a53f469e
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Citations in the corpus
- Self-assembling protein nanoparticles in the design of vaccines (2015, neutral): “Structural proteins fromdifferentmicroorganisms have served as templates for the production of such nanoparticles and for the presentation of immunogenic epitopes: the protein pIII of the filamentous phage f1 [18], the Ty component from Saccharomyces cerevisiae [19], the surface and core antigens of”
- A review of clinical trials of human papillomavirus prophylactic vaccines. (2012, background): “Two phase III studies, FUTURE I [14] and FUTURE II [15], evaluated Gardasil® and two, PATRICIA [16] and the Costa Rica HPV Vaccine Trial (CVT) [17] evaluated Cervarix®.”
- Bio-inspired, bioengineered and biomimetic drug delivery carriers (2011, background): “The HPV-like particles resembled authentic HPV virions and induced protective immune responses against HP”
- Human papillomavirus vaccines: WHO position paper. (2009, background): “Among females naive to HPV-16 or HPV-18 for up to 1 month following the third dose of vaccine, protection against these combined end-points was 100% (95% confidence interval [CI], 94e100%) after a mean follow-up of 3 years [17].”
- Impact of human papillomavirus (HPV)-6/11/16/18 vaccine on all HPV-associated genital diseases in young women. (2010, methodology): “The FUTURE II Study Group.”