Skip to main content
  • ASM
    • Antimicrobial Agents and Chemotherapy
    • Applied and Environmental Microbiology
    • Clinical Microbiology Reviews
    • Clinical and Vaccine Immunology
    • EcoSal Plus
    • Eukaryotic Cell
    • Infection and Immunity
    • Journal of Bacteriology
    • Journal of Clinical Microbiology
    • Journal of Microbiology & Biology Education
    • Journal of Virology
    • mBio
    • Microbiology and Molecular Biology Reviews
    • Microbiology Resource Announcements
    • Microbiology Spectrum
    • Molecular and Cellular Biology
    • mSphere
    • mSystems
  • Log in
  • My Cart

Main menu

  • Home
  • Articles
    • Archive
  • About the Journal
    • About CVI
    • For Librarians
    • For Advertisers
    • FAQ
  • ASM
    • Antimicrobial Agents and Chemotherapy
    • Applied and Environmental Microbiology
    • Clinical Microbiology Reviews
    • Clinical and Vaccine Immunology
    • EcoSal Plus
    • Eukaryotic Cell
    • Infection and Immunity
    • Journal of Bacteriology
    • Journal of Clinical Microbiology
    • Journal of Microbiology & Biology Education
    • Journal of Virology
    • mBio
    • Microbiology and Molecular Biology Reviews
    • Microbiology Resource Announcements
    • Microbiology Spectrum
    • Molecular and Cellular Biology
    • mSphere
    • mSystems

User menu

  • Log in
  • My Cart

Search

  • Advanced search
Clinical and Vaccine Immunology
publisher-logosite-logo

Advanced Search

  • Home
  • Articles
    • Archive
  • About the Journal
    • About CVI
    • For Librarians
    • For Advertisers
    • FAQ
VACCINE RESEARCH

DNA Vaccination by Electroporation and Boosting with Recombinant Proteins Enhances the Efficacy of DNA Vaccines for Schistosomiasis Japonica

Yang Dai, Yinchang Zhu, Donald A. Harn, Xiaoting Wang, Jianxia Tang, Song Zhao, Fei Lu, Xiaohong Guan
Yang Dai
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Yinchang Zhu
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: yczhu2006@yahoo.com.cn
Donald A. Harn
2Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Xiaoting Wang
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jianxia Tang
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Song Zhao
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Fei Lu
1Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, and Jiangsu Provincial Key Subject on Parasitic Diseases, Wuxi 214064, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Xiaohong Guan
3Key Laboratory of Antibody Technique, Ministry of Health, Nanjing Medical University, Nanjing 210029, China
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1128/CVI.00231-09
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • FIG. 1.
    • Open in new tab
    • Download powerpoint
    FIG. 1.

    Levels of IgG, IgG1, and IgG2a antibodies to vaccine antigen(s) in experiment I. Sera were collected as described in Materials and Methods and tested by ELISA for IgG, IgG1, and IgG2a antibodies against pooled vaccine antigens. Levels of IgG in group E (cocktail DNA and protein vaccines) were significantly higher than in group D (cocktail DNA vaccines) (P < 0.01); levels of IgG in group H (cocktail DNA vaccines with EP) were significantly higher than in group D (P < 0.01); levels of IgG in group I (cocktail DNA with EP and protein vaccines) were significantly higher than in group E (P < 0.01) or group H (P < 0.01).

  • FIG. 2.
    • Open in new tab
    • Download powerpoint
    FIG. 2.

    Levels of IgG, IgG1, and IgG2a antibodies to vaccine antigen(s) in experiment II. An ELISA to determine levels of vaccine antigen(s)-specific IgG, IgG1, and IgG2a was conducted as described in Materials and Methods. Levels of IgG in group d (cocktail DNA and protein vaccines) were significantly higher than in group c (cocktail DNA vaccines) (P < 0.01); levels of IgG in group e (cocktail DNA vaccine with EP) were significantly higher than in group c (P < 0.01); levels of IgG in group h (TPI with EP) were significantly higher than in group g (TPI) (P < 0.05); levels of IgG in group f (cocktail DNA with and protein vaccines) were significantly higher than in group d (P < 0.01) and group e (P < 0.01).

Tables

  • Figures
  • TABLE 1.

    Protective efficacies of different vaccination regimens against Schistosoma japonicum challenge infection (experiment I)a

    GroupNo. of miceTotal no. of worms% Worm reductionNo. of eggs in liver% Egg reduction
    A (blank control)1125.82 ± 3.2562,001 ± 9,814
    B (pcDNA3.1)1025.40 ± 2.4661,761 ± 13,787
    C (pcDNA3.1 and cocktail protein vaccines)1221.25 ± 3.1217.7056,182 ± 9,4049.39
    D (cocktail DNA vaccines)917.33 ± 2.7432.8839,559 ± 10,77236.20
    E (cocktail DNA and protein vaccines)914.11 ± 3.5545.3531,908 ± 5,55348.54
    F (pcDNA3.1 with EP)1025.30 ± 3.8058,272 ± 11,680
    G (pcDNA3.1 with EP and cocktail protein vaccines)1321.15 ± 3.4418.0954,257 ± 15,11712.49
    H (cocktail DNA vaccines with EP)1014.20 ± 3.1245.0030,453 ± 8,11450.88
    I (cocktail DNA with EP and protein vaccines)1211.08 ± 3.4257.0925,259 ± 8,43659.26
    • ↵ a Values for worm and egg numbers are means ± standard deviations. Worm and egg reduction rates of each vaccine group were compared to group A (blank control). Statistically significant differences in egg reduction rates were seen in group E versus group C (P < 0.01) or group D (P < 0.05). Worm and egg burdens were significantly reduced in group H versus group D (P < 0.05); also, worm and egg burdens were significantly reduced in group I compared to group E (P < 0.05) or group H (P < 0.05).

  • TABLE 2.

    Protective efficacies of different vaccination regimens against Schistosoma japonicum infection (experiment II)a

    GroupNo. of miceTotal no. of worms% Worm reductionNo. of female worms% Female-worm reductionNo. of eggs in liver% Egg reduction
    a (pcDNA3.1)1022.40 ± 2.5910.10 ± 3.3864,849 ± 11,452
    b (pcDNA3.1 with EP and cocktail protein vaccines)1119.09 ± 3.5414.777.00 ± 2.4430.6951,479 ± 9,83320.62
    c (cocktail DNA vaccines)915.11 ± 2.0932.545.33 ± 3.3547.1936,275 ± 13,06944.06
    d (cocktail DNA and protein vaccines)912.56 ± 1.9443.953.78 ± 1.3962.6027,513 ± 8,18157.57
    e (cocktail DNA vaccine with EP)913.11 ± 2.7141.474.67 ± 1.7353.8030,592 ± 3,37952.83
    f (cocktail DNA with EP and protein vaccines)109.10 ± 3.2159.382.80 ± 1.2372.2821,081 ± 11,85667.49
    g (TPI)1016.30 ± 2.3627.236.50 ± 1.5135.6447,180 ± 10,73527.25
    h (TPI with EP)1112.91 ± 2.5942.375.09 ± 2.1749.6037,127 ± 10,95342.75
    • ↵ a Values for worm and egg counts are means ± standard deviations. Adult worm and liver egg reduction rates were calculated for each group in comparison to group a. Statistically significant differences in adult worm and liver egg burdens were seen for the following comparisons: between group d and group b (P < 0.01) or group c (P < 0.05); between group e and group c (P < 0.05); between group h and group g (TPI) (P < 0.01); and between group f and group d (P < 0.05) or group e (P < 0.01).

  • TABLE 3.

    Boosting with cocktail DNA vaccines by electroporation or with cocktail protein vaccines leads to enhanced production of IL-2 and IFN-γ (experiment I)

    GroupIL-2 (pg/ml)aIFN-γ (pg/ml)a
    BlankConASEABlankConASEA
    A<1011.3810.01<10<10<10
    B<10<1011.11<10<1017.58
    C<1018.5024.90<1019.5436.70
    D<1020.9059.21<10120.72492.31
    E<1023.9768.02<10123.86503.90
    F<10<10<10<1011.9539.55
    G<1021.4652.94<1027.5883.15
    H<1039.1579.28<10300.79625.55
    I<1043.92112.02<1097.05664.23
    • ↵ a Data are average values of readings from triplicate wells for each group.

  • TABLE 4.

    Boosting by electroporation or with cocktail protein vaccines leads to enhanced production of IL-2 and IFN-γ (experiment II)

    GroupIL-2 (pg/ml)aIFN-γ (pg/ml)a
    BlankConASEABlankConASEA
    a<1037.5413.11<1038.9726.56
    b<1091.99111.48<1035.35197.98
    c<1045.39234.68<1049.32439.27
    d<1075.33270.74<1075.33546.32
    e<1089.65254.71<1096.71896.43
    f<1043.17431.73<1092.671,398.04
    g<1031.72110.30<1065.04265.04
    h<1074.32231.28<1083.43318.23
    • ↵ a Data are average values of readings from triplicate wells for each group.

PreviousNext
Back to top
Download PDF
Citation Tools
DNA Vaccination by Electroporation and Boosting with Recombinant Proteins Enhances the Efficacy of DNA Vaccines for Schistosomiasis Japonica
Yang Dai, Yinchang Zhu, Donald A. Harn, Xiaoting Wang, Jianxia Tang, Song Zhao, Fei Lu, Xiaohong Guan
Clinical and Vaccine Immunology Nov 2009, 16 (12) 1796-1803; DOI: 10.1128/CVI.00231-09

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Print

Email

Thank you for sharing this Clinical and Vaccine Immunology article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
DNA Vaccination by Electroporation and Boosting with Recombinant Proteins Enhances the Efficacy of DNA Vaccines for Schistosomiasis Japonica
(Your Name) has forwarded a page to you from Clinical and Vaccine Immunology
(Your Name) thought you would be interested in this article in Clinical and Vaccine Immunology.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
DNA Vaccination by Electroporation and Boosting with Recombinant Proteins Enhances the Efficacy of DNA Vaccines for Schistosomiasis Japonica
Yang Dai, Yinchang Zhu, Donald A. Harn, Xiaoting Wang, Jianxia Tang, Song Zhao, Fei Lu, Xiaohong Guan
Clinical and Vaccine Immunology Nov 2009, 16 (12) 1796-1803; DOI: 10.1128/CVI.00231-09
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Top
  • Article
    • ABSTRACT
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • ACKNOWLEDGMENTS
    • FOOTNOTES
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

KEYWORDS

Antigens, Helminth
Helminth Proteins
Membrane Proteins
Recombinant Proteins
Schistosoma japonicum
Schistosomiasis japonica
Vaccines, DNA

Related Articles

Cited By...

About

  • About CVI
  • For Librarians
  • For Advertisers
  • FAQ
  • Permissions
  • Journal Announcements

Authors

  • Submit a Manuscript to mSphere

ASM Journals

ASM journals are the most prominent publications in the field, delivering up-to-date and authoritative coverage of both basic and clinical microbiology.

About ASM | Contact Us | Press Room

 

ASM is a member of

Scientific Society Publisher Alliance

 

American Society for Microbiology
1752 N St. NW
Washington, DC 20036
Phone: (202) 737-3600

Copyright © 2021 American Society for Microbiology | Privacy Policy | Website feedback

Print ISSN: 1556-6811; Online ISSN: 1556-679X