dc.contributor.author | Craig, Andrew P | |
dc.contributor.author | Gray, Richard T | |
dc.contributor.author | Edwards, Jennifer L | |
dc.contributor.author | Apicella, Michael A | |
dc.contributor.author | Jennings, Michael P | |
dc.contributor.author | Wilson, David P | |
dc.contributor.author | Seib, Kate L | |
dc.date.accessioned | 2017-08-04T07:06:35Z | |
dc.date.available | 2017-08-04T07:06:35Z | |
dc.date.issued | 2015 | |
dc.identifier.issn | 0264-410X | |
dc.identifier.doi | 10.1016/j.vaccine.2015.07.015 | |
dc.identifier.uri | http://hdl.handle.net/10072/124986 | |
dc.description.abstract | Gonorrhea, one of the most common sexually transmitted infections worldwide, can lead to serious sequelae, including infertility and increased HIV transmission. Recently, untreatable, multidrug-resistant Neisseria gonorrhoeae strains have been reported. In the absence of new antibiotics, and given the speed with which resistance has emerged to all previously used antibiotics, development of a vaccine would be the ideal solution to this public health emergency. Understanding the desired characteristics, target population, and expected impact of an anti-gonococcal vaccine is essential to facilitate vaccine design, assessment and implementation. The modeling presented herein aims to fill these conceptual gaps, and inform future gonococcal vaccine development. Using an individual-based, epidemiological simulation model, gonococcal prevalence was simulated in a heterosexual population of 100,000 individuals after the introduction of vaccines with varied efficacy (10–100%) and duration of protection (2.5–20 years). Model simulations predict that gonococcal prevalence could be reduced by at least 90% after 20 years, if all 13-year-olds were given a non-waning vaccine with 50% efficacy, or a vaccine with 100% efficacy that wanes after 7.5 years. A 40% reduction in prevalence is achievable with a non-waning vaccine of only 20% efficacy. We conclude that a vaccine of moderate efficacy and duration could have a substantive impact on gonococcal prevalence, and disease sequelae, if coverage is high and protection lasts over the highest risk period (i.e., most sexual partner change) among young people. | |
dc.description.peerreviewed | Yes | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartofpagefrom | 4520 | |
dc.relation.ispartofpageto | 4525 | |
dc.relation.ispartofissue | 36 | |
dc.relation.ispartofjournal | Vaccine | |
dc.relation.ispartofvolume | 33 | |
dc.subject.fieldofresearch | Biological sciences | |
dc.subject.fieldofresearch | Agricultural, veterinary and food sciences | |
dc.subject.fieldofresearch | Biomedical and clinical sciences | |
dc.subject.fieldofresearch | Immunology not elsewhere classified | |
dc.subject.fieldofresearchcode | 31 | |
dc.subject.fieldofresearchcode | 30 | |
dc.subject.fieldofresearchcode | 32 | |
dc.subject.fieldofresearchcode | 320499 | |
dc.title | The potential impact of vaccination on the prevalence of gonorrhea | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dc.type.code | C - Journal Articles | |
dcterms.license | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.description.version | Version of Record (VoR) | |
gro.rights.copyright | © 2015 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, providing that the work is properly cited. You may not alter, transform, or build upon this work. | |
gro.hasfulltext | Full Text | |
gro.griffith.author | Jennings, Michael P. | |
gro.griffith.author | Seib, Kate | |