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    Potent monoclonal antibodies against Clostridium difficile toxin A elicited by DNA immunization

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    Authors
    Zhang, Chunhua
    Jin, Ke
    Xiao, Yanling
    Cheng, Ying
    Huang, Zuhu
    Wang, Shixia
    Lu, Shan
    UMass Chan Affiliations
    Department of Medicine, Division of Infectious Diseases and Immunology
    Document Type
    Journal Article
    Publication Date
    2013-10-01
    Keywords
    Animals
    Antibodies, Bacterial
    Antibodies, Monoclonal
    Bacterial Toxins
    Enterotoxins
    Immunization
    Mice, Inbred BALB C
    Vaccines, DNA
    Biological Factors
    Genetics and Genomics
    Immunology and Infectious Disease
    Immunology of Infectious Disease
    Immunoprophylaxis and Therapy
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    Link to Full Text
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906400/
    Abstract
    Recent studies have demonstrated that DNA immunization is effective in eliciting antigen-specific antibody responses against a wide range of infectious disease targets. The polyclonal antibodies elicited by DNA vaccination exhibit high sensitivity to conformational epitopes and high avidity. However, there have been limited reports in literature on the production of monoclonal antibodies (mAb) by DNA immunization. Here, by using Clostridium difficile (C. diff) toxin A as a model antigen, we demonstrated that DNA immunization was effective in producing a panel of mAb that are protective against toxin A challenge and can also be used as sensitive reagents to detect toxin A from various testing samples. The immunoglobulin (Ig) gene usage for such mAb was also investigated. Further studies should be conducted to fully establish DNA immunization as a unique platform to produce mAb in various hosts.
    Source
    Hum Vaccin Immunother. 2013 Oct;9(10):2157-64. doi: 10.4161/hv.25656. Epub 2013 Jul 12. Link to article on publisher's site
    DOI
    10.4161/hv.25656
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/30511
    PubMed ID
    23851482
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.4161/hv.25656
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