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      KCI등재 SCIE SCOPUS

      Immune Effect of Newcastle Disease Virus DNA Vaccine with C3d as a Molecular Adjuvant = Immune Effect of Newcastle Disease Virus DNA Vaccine with C3d as a Molecular Adjuvant

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      https://www.riss.kr/link?id=A104186391

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      다국어 초록 (Multilingual Abstract)

      Newcastle disease is a serious infectious disease in the poultry industry. The commercial vaccines can only offer limited protection and some of them are expensive and need adjuvants. At present, DNA vaccines are widely used. However, the immune respo...

      Newcastle disease is a serious infectious disease in the poultry industry. The commercial vaccines can only offer limited protection and some of them are expensive and need adjuvants. At present, DNA vaccines are widely used. However, the immune responses induced by DNA vaccines are too slow and low. Here, we constructed the transfer vectors with a different number of C3d as molecular adjuvants (n = 1, 2, 4, or 6), and the vectors were cloned into the optimal eukaryotic expression plasmid (pVAXI-optiF) that expressed the F gene of Newcastle disease virus (NDV), and named pVAXI-F(o)-C3d1, pVAXI -F(o)-C3d2, pVAXI-F(o)-C3d4, and pVAXI-F(o)-C3d6, respectively. Cell transfection test indicated that pVAXI-F(o)-C3d6 showed the highest expression. In vivo immunization showed that the chickens immunized with pVAXI-F(o)-C3d6 intramuscularly induced better immune responses than the chickens immunized with the other plasmids. The protective efficacy of pVAXI-F(o)-C3d6 was 80% after challenge with the highly virulent NDV strain F48E9. The results in this study showed that C3d6 could be used as a molecular adjuvant to quickly induce an effective immune response to control NDV.

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      참고문헌 (Reference)

      1 Dortmans JC, "The viral replication complex is associated with the virulence of Newcastle disease virus" 84 : 10113-10120, 2010

      2 Zhang Y, "The solvent at antigen-binding site regulated C3d-CR2 interactions through the C-terminal tail of C3d at different ion strengths:insights from molecular dynamics simulation" 1860 : 2220-2231, 2016

      3 Dimitrov KM, "Temporal, geographic, and host distribution of avian paramyxovirus 1 (Newcastle disease virus)" 39 : 22-34, 2016

      4 Zhao K, "Synthesis, characterization and immune efficacy of LDH@SiO2nanoparticles with shell-core structure as a delivery carrier for Newcastle disease virus DNA vaccine" 10 : 2895-2911, 2015

      5 Wu Y, "Recombinant Newcastle disease virus (NDV/Anh-IL-2)expressing human IL-2 as a potential candidate for suppresses growth of hepatoma therapy" 132 : 24-30, 2016

      6 Nagai Y, "Proteolytic cleavage of the viral glycoproteins and its significance for the virulence of Newcastle disease virus" 72 : 494-508, 1976

      7 Li GX, "Prime-boost immunization with HA/C3d DNA followed by a recombinant pseudorabies virus boost enhanced protective immunity against H3N2 swine influenza virus in mice" 88 : 345-351, 2010

      8 Liu XF, "Pathotypical and genotypical characterization of Newcastle disease virus isolated from outbreaks in chicken and goose flocks in some regions of China during 1985-2001" 148 : 1387-1403, 2003

      9 Oreskovic Z, "Oil-based adjuvants delivered intradermally induce high primary IgG2 immune response in swine" 114 : 41-43, 2017

      10 Crépeaux G, "Nonlinear dose-response of aluminium hydroxide adjuvant particles: selective low dose neurotoxicity" 375 : 48-57, 2017

      1 Dortmans JC, "The viral replication complex is associated with the virulence of Newcastle disease virus" 84 : 10113-10120, 2010

      2 Zhang Y, "The solvent at antigen-binding site regulated C3d-CR2 interactions through the C-terminal tail of C3d at different ion strengths:insights from molecular dynamics simulation" 1860 : 2220-2231, 2016

      3 Dimitrov KM, "Temporal, geographic, and host distribution of avian paramyxovirus 1 (Newcastle disease virus)" 39 : 22-34, 2016

      4 Zhao K, "Synthesis, characterization and immune efficacy of LDH@SiO2nanoparticles with shell-core structure as a delivery carrier for Newcastle disease virus DNA vaccine" 10 : 2895-2911, 2015

      5 Wu Y, "Recombinant Newcastle disease virus (NDV/Anh-IL-2)expressing human IL-2 as a potential candidate for suppresses growth of hepatoma therapy" 132 : 24-30, 2016

      6 Nagai Y, "Proteolytic cleavage of the viral glycoproteins and its significance for the virulence of Newcastle disease virus" 72 : 494-508, 1976

      7 Li GX, "Prime-boost immunization with HA/C3d DNA followed by a recombinant pseudorabies virus boost enhanced protective immunity against H3N2 swine influenza virus in mice" 88 : 345-351, 2010

      8 Liu XF, "Pathotypical and genotypical characterization of Newcastle disease virus isolated from outbreaks in chicken and goose flocks in some regions of China during 1985-2001" 148 : 1387-1403, 2003

      9 Oreskovic Z, "Oil-based adjuvants delivered intradermally induce high primary IgG2 immune response in swine" 114 : 41-43, 2017

      10 Crépeaux G, "Nonlinear dose-response of aluminium hydroxide adjuvant particles: selective low dose neurotoxicity" 375 : 48-57, 2017

      11 Wang G, "Non-thermal plasma for inactivated-vaccine preparation" 34 : 1126-1132, 2016

      12 Kumar S, "Newcastle disease virus outbreaks in India:time to revisit the vaccine type and strategies" 33 : 3268-3269, 2015

      13 Kim SH, "Newcastle disease virus as a vaccine vector for development of human and veterinary vaccines" 8 : 2-15, 2016

      14 Li L, "Molecular mechanisms for enhanced DNA vaccine immunogenicity" 15 : 313-329, 2016

      15 Morla S, "Molecular characterization of genotype XIIIb Newcastle disea se v irus f rom centra l India during 2006-2012: evidence of its panzootic potential" 99 : 83-86, 2016

      16 Buonavoglia D, "Long-term immunogenicity and protection against Mycoplasma agalactiae induced by an oil adjuvant vaccine in sheep" 88 : 16-19, 2010

      17 Tlaxca JL, "Live attenuated and inactivated viral vaccine formulation and nasal delivery:potential and challenges" 93 : 56-78, 2015

      18 Xu GL, "Induction of protective and therapeutic antitumor immunity by a DNA vaccine with C3d as a molecular adjuvant" 28 : 7221-7227, 2010

      19 Miller PJ, "Identification of new sub-genotypes of virulent Newcastle disease virus with potential panzootic features" 29 : 216-229, 2015

      20 Wang J, "Genomic characterizations of a Newcastle disease virus isolated from ducks in live bird markets in China" 11 : e0158771-, 2016

      21 Hao HF, "Genetic variation in V gene of class II Newcastle disease virus" 37 : 14-20, 2016

      22 Suradhat S, "Fusion of C3d molecule with bovine rotavirus VP7 or bovine herpesvirus type 1 glycoprotein D inhibits immune responses following DNA immunization" 83 : 79-92, 2001

      23 Ramezanpour B, "Emergency deployment of genetically engineered veterinary vaccines in Europe" 34 : 3435-3440, 2016

      24 Cardenas-Garcia S, "Effects of chicken interferon gamma on Newcastle disease virus vaccine immunogenicity" 11 : e0159153-, 2016

      25 Cardenas-Garcia S, "Development of an improved vaccine evaluation protocol to compare the efficacy of Newcastle disease vaccines" 43 : 136-145, 2015

      26 DiNapoli JM, "Delivery to the lower respiratory tract is required for effective immunization with Newcastle disease virus-vectored vaccines intended for humans" 27 : 1530-1539, 2009

      27 Liu D, "Cloning of a gene fragment encoding chicken complement component C3d with expression and immunogenicity of Newcastle disease virus F gene-C3d fusion protein" 37 : 477-485, 2008

      28 Musa HH, "Cloning and expression of FimA-C3d recombinant protein" 12 : 55-59, 2014

      29 Steglich C, "Chimeric avian paramyxovirusbased vector immunization against highly pathogenic avian influenza followed by conventional Newcastle disease vaccination eliminates lack of protection from virulent ND virus" 3 : 65-72, 2014

      30 Dempsey PW, "C3d of complement as a molecular adjuvant:bridging innate and acquired immunity" 271 : 348-350, 1996

      31 Wang R, "Boosting of DNA vaccine-elicited gamma interferon responses in humans by exposure to malaria parasites" 73 : 2863-2872, 2005

      32 Baxter D., "Active and passive immunity, vaccine types, excipients and licensing" 57 : 552-556, 2007

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      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-04-04 학술지명변경 한글명 : -> Journal of Microbiology and Biotechnology KCI등재
      2006-03-30 학술지등록 한글명 :
      외국어명 : Journal of Microbiology and Biotechnology
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      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.59 0.33 1.17
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.91 0.78 0.472 0.08
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