Review
- MINIREVIEW] Advances in novel influenza vaccines: a patent review
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Jae-Min Song
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J. Microbiol. 2016;54(6):403-412. Published online May 27, 2016
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DOI: https://doi.org/10.1007/s12275-016-6176-7
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Abstract
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The threat of a major human influenza pandemic such as
the avian H5N1 or the 2009 new H1N1 has emphasized the
need for effective prevention strategies to combat these pathogens.
Although egg based influenza vaccines have been well
established for a long time, it remains an ongoing public
health need to develop alternative production methods that
ensures improved safety, efficacy, and ease of administration
compared with conventional influenza vaccines. This article
is intended to cover some of the recent advances and related
patents on the development of influenza vaccines including
live attenuated, cell based, genomic and synthetic peptide
vaccines.
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Citations
Citations to this article as recorded by

- Plant-made virus-like particles bearing influenza hemagglutinin (HA) recapitulate early interactions of native influenza virions with human monocytes/macrophages
Alexander I. Makarkov, Sabrina Chierzi, Stéphane Pillet, Keith K. Murai, Nathalie Landry, Brian J. Ward
Vaccine.2017; 35(35): 4629. CrossRef
Research Support, Non-U.S. Gov't
- A Potent Brucella abortus 2308 Δery Live Vaccine Allows for the Differentiation between Natural and Vaccinated Infection
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Junbo Zhang , Shuanghong Yin , Fei Guo , Ren Meng , Chuangfu Chen , Hui Zhang , Zhiqiang Li , Qiang Fu , Huijun Shi , Shengwei Hu , Wei Ni , Tiansen Li , Ke Zhang
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J. Microbiol. 2014;52(8):681-688. Published online July 4, 2014
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DOI: https://doi.org/10.1007/s12275-014-3689-9
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Abstract
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Brucellosis is a globally distributed zoonotic disease that causes animal and human diseases. However, the current Brucella abortus vaccines (S19 and RB51) are deficient; they can cause abortion in pregnant animals. Moreover, when the
vaccine S19 is used, tests cannot differentiate natural from vaccinated infection. Therefore, a safer and more potent vaccine is needed. A Brucella abortus 2308 ery promoter mutant (Δery) was constructed to overcome these drawbacks. The growth of the Δery mutant was significantly attenuated in macrophages and mice and induced high protective immunity in mice. Moreover, Δery induced an anti-Brucellaspecific IgG (immunoglobulin G) response and stimulated the expression of interferon-gamma (INF-γ) and interleukin-4 (IL-4). Furthermore, the expression of EryA antigen allowed for the serological differentiation between natural and vaccinated infection in mice. These results indicate that the Δery mutant is a potential attenuated live vaccine candidate against virulent Brucella abortus 2308 (S2308) infection.
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Citations
Citations to this article as recorded by

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