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Erschienen in: Archives of Virology 6/2016

15.03.2016 | Original Article

A novel dengue virus serotype 1 vaccine candidate based on Japanese encephalitis virus vaccine strain SA14-14-2 as the backbone

verfasst von: Huiqiang Yang, Zhushi Li, Hua Lin, Wei Wang, Jian Yang, Lina Liu, Xianwu Zeng, Yonglin Wu, Yongxin Yu, Yuhua Li

Erschienen in: Archives of Virology | Ausgabe 6/2016

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Abstract

To develop a potential dengue vaccine candidate, a full-length cDNA clone of a novel chimeric virus was constructed using recombinant DNA technology, with Japanese encephalitis virus (JEV) vaccine strain SA14-14-2 as the backbone, with its premembrane (prM) and envelope (E) genes substituted by their counterparts from dengue virus type 1 (DENV1). The chimeric virus (JEV/DENV1) was successfully recovered from primary hamster kidney (PHK) cells by transfection with the in vitro transcription products of JEV/DENV1 cDNA and was identified by complete genome sequencing and immunofluorescent staining. No neuroinvasiveness of this chimeric virus was observed in mice inoculated by the subcutaneous route (s.c.) or by the intraperitoneal route (i.p.), while some neurovirulence was displayed in mice that were inoculated directly by the intracerebral route (i.c.). The chimeric virus was able to stimulate high-titer production of antibodies against DENV1 and provided protection against lethal challenge with neuroadapted dengue virus in mice. These results suggest that the chimeric virus is a promising dengue vaccine candidate.
Literatur
3.
Zurück zum Zitat Back AT, Lundkvist A (2013) Dengue viruses—an overview. Infect Ecol Epidemiol 67:171–179, 301–305. doi:10.1038/nrmicro2460 Back AT, Lundkvist A (2013) Dengue viruses—an overview. Infect Ecol Epidemiol 67:171–179, 301–305. doi:10.1038/nrmicro2460
6.
Zurück zum Zitat Roberts CH, Mongkolsapaya J, Screaton G (2012) Dengue fever: a practical guide. Br J Hosp Med (Lond) 73:C60–C64 Roberts CH, Mongkolsapaya J, Screaton G (2012) Dengue fever: a practical guide. Br J Hosp Med (Lond) 73:C60–C64
8.
Zurück zum Zitat Miller N (2010) Recent progress in dengue vaccine research and development. Curr Opin Mol Ther 12:31–38PubMed Miller N (2010) Recent progress in dengue vaccine research and development. Curr Opin Mol Ther 12:31–38PubMed
15.
Zurück zum Zitat Sabchareon A, Wallace D, Sirivichayakul C, Limkittikul K, Chanthavanich P, Suvannadabba S, Jiwariyavej V, Dulyachai W, Pengsaa K, Wartel TA, Moureau A, Saville M, Bouckenooghe A, Viviani S, Tornieporth NG, Lang J (2012) Protective efficacy of the recombinant, live-attenuated, CYD tetravalent dengue vaccine in Thai schoolchildren: a randomised, controlled phase 2b trial. Lancet 380:1559–1567. doi:10.1016/S0140-6736(12)61428-7 CrossRefPubMed Sabchareon A, Wallace D, Sirivichayakul C, Limkittikul K, Chanthavanich P, Suvannadabba S, Jiwariyavej V, Dulyachai W, Pengsaa K, Wartel TA, Moureau A, Saville M, Bouckenooghe A, Viviani S, Tornieporth NG, Lang J (2012) Protective efficacy of the recombinant, live-attenuated, CYD tetravalent dengue vaccine in Thai schoolchildren: a randomised, controlled phase 2b trial. Lancet 380:1559–1567. doi:10.​1016/​S0140-6736(12)61428-7 CrossRefPubMed
16.
Zurück zum Zitat Dayan GH, Garbes P, Noriega F, Izoton de Sadovsky AD, Rodrigues PM, Giuberti C, Dietze R (2013) Immunogenicity and safety of a recombinant tetravalent dengue vaccine in children and adolescents ages 9–16 years in Brazil. Am J Trop Med Hyg 89:1058–1065. doi:10.4269/ajtmh.13-0304 CrossRefPubMedPubMedCentral Dayan GH, Garbes P, Noriega F, Izoton de Sadovsky AD, Rodrigues PM, Giuberti C, Dietze R (2013) Immunogenicity and safety of a recombinant tetravalent dengue vaccine in children and adolescents ages 9–16 years in Brazil. Am J Trop Med Hyg 89:1058–1065. doi:10.​4269/​ajtmh.​13-0304 CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Capeding MR, Tran NH, Hadinegoro SR, Ismail HI, Chotpitayasunondh T, Chua MN, Luong CQ, Rusmil K, Wirawan DN, Nallusamy R et al (2014) Clinical efficacy and safety of a novel tetravalent dengue vaccine in healthy children in Asia: a phase 3, randomised, observer-masked, placebo-controlled trial. Lancet 384:1358–1365. doi:10.1016/S0140-6736(14)61060-6 CrossRefPubMed Capeding MR, Tran NH, Hadinegoro SR, Ismail HI, Chotpitayasunondh T, Chua MN, Luong CQ, Rusmil K, Wirawan DN, Nallusamy R et al (2014) Clinical efficacy and safety of a novel tetravalent dengue vaccine in healthy children in Asia: a phase 3, randomised, observer-masked, placebo-controlled trial. Lancet 384:1358–1365. doi:10.​1016/​S0140-6736(14)61060-6 CrossRefPubMed
19.
Zurück zum Zitat Villar L, Dayan GH, Arredondo-García JL, Rivera DM, Cunha R, Deseda C, Reynales H, Costa MS et al (2015) Efficacy of a tetravalent dengue vaccine in children in Latin America. N Engl J Med 372:113–123. doi:10.1056/NEJMoa1411037 CrossRefPubMed Villar L, Dayan GH, Arredondo-García JL, Rivera DM, Cunha R, Deseda C, Reynales H, Costa MS et al (2015) Efficacy of a tetravalent dengue vaccine in children in Latin America. N Engl J Med 372:113–123. doi:10.​1056/​NEJMoa1411037 CrossRefPubMed
20.
Zurück zum Zitat Coudeville L, Baurin N, Vergu E (2015) Estimation of parameters related to vaccine efficacy and dengue transmission from two large phase III studies. Vaccine. doi:10.1016/j.vaccine (Epub ahead of print) Coudeville L, Baurin N, Vergu E (2015) Estimation of parameters related to vaccine efficacy and dengue transmission from two large phase III studies. Vaccine. doi:10.​1016/​j.​vaccine (Epub ahead of print)
22.
Zurück zum Zitat Fahimi H, Allahyari H, Hassan ZM, Sadeghizadeh M (2014) Dengue virus type-3 envelope protein domain III; expression and immunogenicity. Iran J Basic Med Sci 17:836–843PubMedPubMedCentral Fahimi H, Allahyari H, Hassan ZM, Sadeghizadeh M (2014) Dengue virus type-3 envelope protein domain III; expression and immunogenicity. Iran J Basic Med Sci 17:836–843PubMedPubMedCentral
27.
Zurück zum Zitat Lindsey NP, Schroeder BA, Miller ER, Braun MM, Hinckley AF, Marano N, Slade BA, Barnett ED, Brunette GW, Horan K, Staples JE, Kozarsky PE, Hayes EB (2008) Adverse event reports following yellow fever vaccination. Vaccine. 26:6077–6082. doi:10.1016/j.vaccine CrossRefPubMed Lindsey NP, Schroeder BA, Miller ER, Braun MM, Hinckley AF, Marano N, Slade BA, Barnett ED, Brunette GW, Horan K, Staples JE, Kozarsky PE, Hayes EB (2008) Adverse event reports following yellow fever vaccination. Vaccine. 26:6077–6082. doi:10.​1016/​j.​vaccine CrossRefPubMed
28.
Zurück zum Zitat Vellozzi C, Mitchell T, Miller E, Casey CG, Eidex RB, Hayes EB (2006) Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) and corticosteroid therapy: eleven United States cases, 1996–2004. Am J Trop Med Hyg 75:333–336PubMed Vellozzi C, Mitchell T, Miller E, Casey CG, Eidex RB, Hayes EB (2006) Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) and corticosteroid therapy: eleven United States cases, 1996–2004. Am J Trop Med Hyg 75:333–336PubMed
30.
Zurück zum Zitat Mathenge Edward Gitau Matumbi, del Carmen Maria, Parquet Yasutomo Funakoshi, Houhara Seiji, Wong Pooi Fong, Ichinose Akitoyo, Hasebe Futoshi, Inoue Shingo, Morita Kouichi (2004) Fusion PCR generated Japanese encephalitis virus/dengue 4 virus chimera exhibits lack of neuroinvasiveness, attenuated neurovirulence, and a dual-flavi immune response in mice. J General Virol 85:2503–2513CrossRef Mathenge Edward Gitau Matumbi, del Carmen Maria, Parquet Yasutomo Funakoshi, Houhara Seiji, Wong Pooi Fong, Ichinose Akitoyo, Hasebe Futoshi, Inoue Shingo, Morita Kouichi (2004) Fusion PCR generated Japanese encephalitis virus/dengue 4 virus chimera exhibits lack of neuroinvasiveness, attenuated neurovirulence, and a dual-flavi immune response in mice. J General Virol 85:2503–2513CrossRef
31.
Zurück zum Zitat Chambers TJ, Jiang X, Droll DA, Liang Y, Wold WS, Nickells J (2006) Chimeric Japanese encephalitis virus/dengue 2 virus infectious clone: biological properties, immunogenicity and protection against dengue encephalitis in mice. J Gen Virol. 87(Pt 11):3131–3140CrossRefPubMed Chambers TJ, Jiang X, Droll DA, Liang Y, Wold WS, Nickells J (2006) Chimeric Japanese encephalitis virus/dengue 2 virus infectious clone: biological properties, immunogenicity and protection against dengue encephalitis in mice. J Gen Virol. 87(Pt 11):3131–3140CrossRefPubMed
32.
Zurück zum Zitat Li XF, Deng YQ, Yang HQ, Zhao H, Jiang T, Yu XD, Li SH, Ye Q, Zhu SY, Wang HJ, Zhang Y, Ma J, Yu YX, Liu ZY, Li YH, Qin ED, Shi PY, Qin CF (2013) A chimeric dengue virus vaccine using Japanese encephalitis virus vaccine strain SA14-14-2 as backbone is immunogenic and protective against either parental virus in mice and nonhuman primates. J Virol 87:13694–13705. doi:10.1128/JVI.00931-13 CrossRefPubMedPubMedCentral Li XF, Deng YQ, Yang HQ, Zhao H, Jiang T, Yu XD, Li SH, Ye Q, Zhu SY, Wang HJ, Zhang Y, Ma J, Yu YX, Liu ZY, Li YH, Qin ED, Shi PY, Qin CF (2013) A chimeric dengue virus vaccine using Japanese encephalitis virus vaccine strain SA14-14-2 as backbone is immunogenic and protective against either parental virus in mice and nonhuman primates. J Virol 87:13694–13705. doi:10.​1128/​JVI.​00931-13 CrossRefPubMedPubMedCentral
33.
Zurück zum Zitat Li Z, Yang H, Yang J, Lin H, Wang W, Liu L, Zhao Y, Liu L, Zeng X, Yu Y, Li Y (2014) Construction and preliminary investigation of a novel dengue serotype 4 chimeric virus using Japanese encephalitis vaccine strain SA14-14-2 as the backbone. Virus Res 191:10–20. doi:10.1016/j.virusres.2014.07.017 CrossRefPubMed Li Z, Yang H, Yang J, Lin H, Wang W, Liu L, Zhao Y, Liu L, Zeng X, Yu Y, Li Y (2014) Construction and preliminary investigation of a novel dengue serotype 4 chimeric virus using Japanese encephalitis vaccine strain SA14-14-2 as the backbone. Virus Res 191:10–20. doi:10.​1016/​j.​virusres.​2014.​07.​017 CrossRefPubMed
38.
Zurück zum Zitat Suzarte E, Marcos E, Gil, L, Valdès I, Lazo L, Ramos Y , Pèrez Y, Falcón V, Romero Y, Guzmón MG, González S, Kouri J, Guillèn G, Hermida L (2014) Generation and characterization of potential dengue vaccine candidates based on domain III of the envelope protein and the capsid protein of the four serotypes of dengue virus. Arch Virol 159:1629–1640. doi:10.1007/s00705-013-1956-4 Suzarte E, Marcos E, Gil, L, Valdès I, Lazo L, Ramos Y , Pèrez Y, Falcón V, Romero Y, Guzmón MG, González S, Kouri J, Guillèn G, Hermida L (2014) Generation and characterization of potential dengue vaccine candidates based on domain III of the envelope protein and the capsid protein of the four serotypes of dengue virus. Arch Virol 159:1629–1640. doi:10.​1007/​s00705-013-1956-4
40.
Zurück zum Zitat Paes MV, Pinhão AT, Barreto DF, Costa SM, Oliveira MP, Nogueira AC, Takiya CM, Farias-Filho JC, Schatzmayr HG, Alves AM, Barth OM (2005) Liver injury and viremia in mice infected with dengue-2 virus. Virology 338:236–246CrossRefPubMed Paes MV, Pinhão AT, Barreto DF, Costa SM, Oliveira MP, Nogueira AC, Takiya CM, Farias-Filho JC, Schatzmayr HG, Alves AM, Barth OM (2005) Liver injury and viremia in mice infected with dengue-2 virus. Virology 338:236–246CrossRefPubMed
41.
Zurück zum Zitat Guirakhoo F, Pugachev K, Zhang Z, Myers G, Levenbook I, Draper K, Lang J, Ocran S, Mitchell F, Parsons M, Brown N, Brandler S, Fournier C, Barrere B, Rizvi F, Travassos A, Nichols R, Trent D, Monath T (2004) Safety and efficacy of chimeric yellow Fever-dengue virus tetravalent vaccine formulations in nonhuman primates. J Virol 78:4761–4775. doi:10.1128/JVI.78.9.4761-4775 CrossRefPubMedPubMedCentral Guirakhoo F, Pugachev K, Zhang Z, Myers G, Levenbook I, Draper K, Lang J, Ocran S, Mitchell F, Parsons M, Brown N, Brandler S, Fournier C, Barrere B, Rizvi F, Travassos A, Nichols R, Trent D, Monath T (2004) Safety and efficacy of chimeric yellow Fever-dengue virus tetravalent vaccine formulations in nonhuman primates. J Virol 78:4761–4775. doi:10.​1128/​JVI.​78.​9.​4761-4775 CrossRefPubMedPubMedCentral
42.
Zurück zum Zitat Guirakhoo F, Pugachev K, Arroyo J, Miller C, Zhang ZX, Weltzin R, Georgakopoulos K, Catalan J, Ocran S, Draper K, Monath TP (2002) Viremia and immunogenicity in nonhuman primates of a tetravalent yellow fever-dengue chimeric vaccine: genetic reconstructions, dose adjustment, and antibody responses against wild-type dengue virus isolates. Virology 298:146–159. doi:10.1006/viro.2002.1462 CrossRefPubMed Guirakhoo F, Pugachev K, Arroyo J, Miller C, Zhang ZX, Weltzin R, Georgakopoulos K, Catalan J, Ocran S, Draper K, Monath TP (2002) Viremia and immunogenicity in nonhuman primates of a tetravalent yellow fever-dengue chimeric vaccine: genetic reconstructions, dose adjustment, and antibody responses against wild-type dengue virus isolates. Virology 298:146–159. doi:10.​1006/​viro.​2002.​1462 CrossRefPubMed
43.
Zurück zum Zitat Chambers TJ, Liang Y, Droll DA et al (2003) Yellow fever virus/dengue-2 virus and yellow fever virus/dengue-4 virus chimeras: biological characterization, immunogenicity, and protection against dengue encephalitis in the mouse model. J Virol 77(6):3655–3668CrossRefPubMedPubMedCentral Chambers TJ, Liang Y, Droll DA et al (2003) Yellow fever virus/dengue-2 virus and yellow fever virus/dengue-4 virus chimeras: biological characterization, immunogenicity, and protection against dengue encephalitis in the mouse model. J Virol 77(6):3655–3668CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat WHO (2011) Guidelines on the quality, safety and efficacy of dengue tetravalent vaccines (live, attenuated). Proposed replacement of annex 2. In: WHO technical report series, No. 979 WHO (2011) Guidelines on the quality, safety and efficacy of dengue tetravalent vaccines (live, attenuated). Proposed replacement of annex 2. In: WHO technical report series, No. 979
45.
Zurück zum Zitat WHO (2013) Recommendations for the evaluation of animal cell cultures as substrates for the manufacture of biological medicinal products and for the characterization of cell banks. Replacement of annex 1, TRS, 878. In: Technical report series 978, annex 3. WHO, Geneva WHO (2013) Recommendations for the evaluation of animal cell cultures as substrates for the manufacture of biological medicinal products and for the characterization of cell banks. Replacement of annex 1, TRS, 878. In: Technical report series 978, annex 3. WHO, Geneva
48.
Zurück zum Zitat Lazo L, Izquierdo A, Suzarte E, Gil L, Valdés I, Marcos E, Álvarez M, Romero Y, Guzmán MG, Guillén G, Hermida Cruz L (2014) Evaluation in mice of the immunogenicity and protective efficacy of a tetravalent subunit vaccine candidate against dengue virus. Microbiol Immunol 58:219–226. doi:10.1111/1348-0421.12140 CrossRefPubMed Lazo L, Izquierdo A, Suzarte E, Gil L, Valdés I, Marcos E, Álvarez M, Romero Y, Guzmán MG, Guillén G, Hermida Cruz L (2014) Evaluation in mice of the immunogenicity and protective efficacy of a tetravalent subunit vaccine candidate against dengue virus. Microbiol Immunol 58:219–226. doi:10.​1111/​1348-0421.​12140 CrossRefPubMed
50.
Zurück zum Zitat Clements DE, Coller BA, Lieberman MM, Ogata S, Wang G, Harada KE, Putnak JR, Ivy JM, McDonell M, Bignami GS, Peters ID, Leung J, Weeks-Levy C, Nakano ET, Humphreys T (2010) Development of a recombinant tetravalent dengue virus vaccine: immunogenicity and efficacy studies in mice and monkeys. Vaccine 28:2705–2715. doi:10.1016/j.vaccine.2010.01.022 CrossRefPubMedPubMedCentral Clements DE, Coller BA, Lieberman MM, Ogata S, Wang G, Harada KE, Putnak JR, Ivy JM, McDonell M, Bignami GS, Peters ID, Leung J, Weeks-Levy C, Nakano ET, Humphreys T (2010) Development of a recombinant tetravalent dengue virus vaccine: immunogenicity and efficacy studies in mice and monkeys. Vaccine 28:2705–2715. doi:10.​1016/​j.​vaccine.​2010.​01.​022 CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat White Laura J, Parsons Melissa M, Whitmore Alan C, Williams Brandon M, de Silva Aravinda, Johnston Robert E (2007) An immunogenic and protective alphavirus replicon particle-based dengue vaccine overcomes maternal antibody interference in weanling mice. J Virol 81:10329–10339. doi:10.1128/JVI.00512-07 CrossRefPubMedPubMedCentral White Laura J, Parsons Melissa M, Whitmore Alan C, Williams Brandon M, de Silva Aravinda, Johnston Robert E (2007) An immunogenic and protective alphavirus replicon particle-based dengue vaccine overcomes maternal antibody interference in weanling mice. J Virol 81:10329–10339. doi:10.​1128/​JVI.​00512-07 CrossRefPubMedPubMedCentral
Metadaten
Titel
A novel dengue virus serotype 1 vaccine candidate based on Japanese encephalitis virus vaccine strain SA14-14-2 as the backbone
verfasst von
Huiqiang Yang
Zhushi Li
Hua Lin
Wei Wang
Jian Yang
Lina Liu
Xianwu Zeng
Yonglin Wu
Yongxin Yu
Yuhua Li
Publikationsdatum
15.03.2016
Verlag
Springer Vienna
Erschienen in
Archives of Virology / Ausgabe 6/2016
Print ISSN: 0304-8608
Elektronische ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-016-2817-8

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