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Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice

BACKGROUND: The incidence of dengue, an infectious disease caused by dengue virus (DENV), has dramatically increased around the world in recent decades and is becoming a severe public health threat. However, there is currently no specific treatment for dengue fever, and licensed vaccine against deng...

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Autores principales: Zhang, Shuo, Liang, Mifang, Gu, Wen, Li, Chuan, Miao, Fang, Wang, Xiaofang, Jin, Cong, Zhang, Li, Zhang, Fushun, Zhang, Quanfu, Jiang, Lifang, Li, Mengfeng, Li, Dexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144018/
https://www.ncbi.nlm.nih.gov/pubmed/21714940
http://dx.doi.org/10.1186/1743-422X-8-333
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author Zhang, Shuo
Liang, Mifang
Gu, Wen
Li, Chuan
Miao, Fang
Wang, Xiaofang
Jin, Cong
Zhang, Li
Zhang, Fushun
Zhang, Quanfu
Jiang, Lifang
Li, Mengfeng
Li, Dexin
author_facet Zhang, Shuo
Liang, Mifang
Gu, Wen
Li, Chuan
Miao, Fang
Wang, Xiaofang
Jin, Cong
Zhang, Li
Zhang, Fushun
Zhang, Quanfu
Jiang, Lifang
Li, Mengfeng
Li, Dexin
author_sort Zhang, Shuo
collection PubMed
description BACKGROUND: The incidence of dengue, an infectious disease caused by dengue virus (DENV), has dramatically increased around the world in recent decades and is becoming a severe public health threat. However, there is currently no specific treatment for dengue fever, and licensed vaccine against dengue is not available. Vaccination with virus-like particles (VLPs) has shown considerable promise for many viral diseases, but the effect of DENV VLPs to induce specific immune responses has not been adequately investigated. RESULTS: By optimizing the expression plasmids, recombinant VLPs of four antigenically different DENV serotypes DENV1-4 were successfully produced in 293T cells. The vaccination effect of dengue VLPs in mice showed that monovalent VLPs of each serotype stimulated specific IgG responses and potent neutralizing antibodies against homotypic virus. Tetravalent VLPs efficiently enhanced specific IgG and neutralizing antibodies against all four serotypes of DENV. Moreover, vaccination with monovalent or tetravalent VLPs resulted in the induction of specific cytotoxic T cell responses. CONCLUSIONS: Mammalian cell expressed dengue VLPs are capable to induce VLP-specific humoral and cellular immune responses in mice, and being a promising subunit vaccine candidate for prevention of dengue virus infection.
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spelling pubmed-31440182011-07-27 Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice Zhang, Shuo Liang, Mifang Gu, Wen Li, Chuan Miao, Fang Wang, Xiaofang Jin, Cong Zhang, Li Zhang, Fushun Zhang, Quanfu Jiang, Lifang Li, Mengfeng Li, Dexin Virol J Research BACKGROUND: The incidence of dengue, an infectious disease caused by dengue virus (DENV), has dramatically increased around the world in recent decades and is becoming a severe public health threat. However, there is currently no specific treatment for dengue fever, and licensed vaccine against dengue is not available. Vaccination with virus-like particles (VLPs) has shown considerable promise for many viral diseases, but the effect of DENV VLPs to induce specific immune responses has not been adequately investigated. RESULTS: By optimizing the expression plasmids, recombinant VLPs of four antigenically different DENV serotypes DENV1-4 were successfully produced in 293T cells. The vaccination effect of dengue VLPs in mice showed that monovalent VLPs of each serotype stimulated specific IgG responses and potent neutralizing antibodies against homotypic virus. Tetravalent VLPs efficiently enhanced specific IgG and neutralizing antibodies against all four serotypes of DENV. Moreover, vaccination with monovalent or tetravalent VLPs resulted in the induction of specific cytotoxic T cell responses. CONCLUSIONS: Mammalian cell expressed dengue VLPs are capable to induce VLP-specific humoral and cellular immune responses in mice, and being a promising subunit vaccine candidate for prevention of dengue virus infection. BioMed Central 2011-06-30 /pmc/articles/PMC3144018/ /pubmed/21714940 http://dx.doi.org/10.1186/1743-422X-8-333 Text en Copyright ©2011 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhang, Shuo
Liang, Mifang
Gu, Wen
Li, Chuan
Miao, Fang
Wang, Xiaofang
Jin, Cong
Zhang, Li
Zhang, Fushun
Zhang, Quanfu
Jiang, Lifang
Li, Mengfeng
Li, Dexin
Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title_full Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title_fullStr Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title_full_unstemmed Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title_short Vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
title_sort vaccination with dengue virus-like particles induces humoral and cellular immune responses in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144018/
https://www.ncbi.nlm.nih.gov/pubmed/21714940
http://dx.doi.org/10.1186/1743-422X-8-333
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