scholarly journals HPV vaccines cut cancer cases

2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Ben Abbott
Keyword(s):  
2016 ◽  
Vol 11 (4) ◽  
pp. 284-289 ◽  
Author(s):  
Vikrant Chadrakant Sangar ◽  
Balasaheb Ghongane ◽  
Gaurav Mathur

Author(s):  
Sedigheh Taghinezhad-S ◽  
Hossein Keyvani ◽  
Luis G. Bermúdez-Humarán ◽  
Gilbert G. G. Donders ◽  
Xiangsheng Fu ◽  
...  

Viruses ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1339
Author(s):  
Kristoffer Juul Nielsen ◽  
Kathrine Kronberg Jakobsen ◽  
Jakob Schmidt Jensen ◽  
Christian Grønhøj ◽  
Christian Von Buchwald

Human papillomavirus (HPV) imposes an increased risk of developing cervical, anal and oropharyngeal cancer. In the Western world, HPV infection is currently the major cause of oropharyngeal cancer. The effectiveness of HPV vaccines for oral or oropharyngeal HPV infection is yet to be determined. This study conducted a systematic literature search in Pubmed and Embase. Studies investigating the impact of HPV vaccines on oral or oropharyngeal HPV infection were enrolled. This review reports the relative prevention percentage (RPP), including a risk of bias assessment as well as a quality assessment study. Nine studies were included (48,777 participants): five cross-sectional studies; one randomized community trial study (RCT); one longitudinal cohort study; and two case-control studies. A significant mean RPP of 83.9% (66.6–97.8%) was calculated from the cross-sectional studies, 82.4% in the included RCT and 83% in the longitudinal cohort study. Further, two case-control studies that measured antibody response in participants immunized with HPV vaccines were included. Respectively, 100% and 93.2% of participants developed HPV-16 Immunoglobulin G (IgG) antibodies in oral fluids post-vaccination. Analysis of the studies identified a significant decrease in vaccine-type oral or oropharyngeal HPV infections in study participants immunized with HPV vaccines across study designs and heterogenous populations. Further, a significant percentage of participants developed IgG antibodies in oral fluid post-vaccination.


Vaccine ◽  
2016 ◽  
Vol 34 (48) ◽  
pp. 5984-5989 ◽  
Author(s):  
Chaevia Clendinen ◽  
Yapei Zhang ◽  
Rebecca N. Warburton ◽  
Donald W. Light

2006 ◽  
Vol 20 (2) ◽  
pp. 279-293 ◽  
Author(s):  
Margaret Stanley
Keyword(s):  

2021 ◽  
Vol 10 (5) ◽  
pp. 1044
Author(s):  
Bettina Huber ◽  
Joshua Weiyuan Wang ◽  
Richard B. S. Roden ◽  
Reinhard Kirnbauer

Licensed human papillomavirus (HPV) vaccines contain virus-like particles (VLPs) self-assembled from L1 major-capsid proteins that are remarkably effective prophylactic immunogens. However, the induced type-restricted immune response limits coverage to the included vaccine types, and costly multiplex formulations, restrictive storage and distribution conditions drive the need for next generation HPV vaccines. Vaccine candidates based upon the minor structural protein L2 are particularly promising because conserved N-terminal epitopes induce broadly cross-type neutralizing and protective antibodies. Several strategies to increase the immunological potency of such epitopes are being investigated, including concatemeric multimers, fusion to toll-like receptors ligands or T cell epitopes, as well as immunodominant presentation by different nanoparticle or VLP structures. Several promising L2-based vaccine candidates have reached or will soon enter first-in-man clinical studies. RG1-VLP present the HPV16L2 amino-acid 17–36 conserved neutralization epitope “RG1” repetitively and closely spaced on an immunodominant surface loop of HPV16 L1-VLP and small animal immunizations provide cross-protection against challenge with all medically-significant high-risk and several low-risk HPV types. With a successful current good manufacturing practice (cGMP) campaign and this promising breadth of activity, even encompassing cross-neutralization of several cutaneous HPV types, RG1-VLP are ready for a first-in-human clinical study. This review aims to provide a general overview of these candidates with a special focus on the RG1-VLP vaccine and its road to the clinic.


2013 ◽  
Vol 8 (1) ◽  
Author(s):  
Lucija Tomljenovic ◽  
Judy Wilyman ◽  
Eva Vanamee ◽  
Toni Bark ◽  
Christopher A Shaw

2016 ◽  
Vol 5 (11) ◽  
pp. 3346-3352 ◽  
Author(s):  
Carmen Radecki Breitkopf ◽  
Lila J. Finney Rutten ◽  
Victoria Findley ◽  
Debra J. Jacobson ◽  
Patrick M. Wilson ◽  
...  

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