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Advancing the Alb-uPA/SCID/Bg Chimeric Mouse

  • Author / Creator
    Hsi Dickie, Belinda
  • The feasibility of the Alb-uPA/SCID/Bg chimeric mouse as a model for Hepatitis C Virus (HCV)
    infection was assessed experimentally by (1) the infection and treatment with another
    hepatotropic virus, Hepatitis B Virus (HBV) and (2) the infection of the model with HCV and the
    subsequent treatment of that infection with a pro-apoptotic factor (BID) targeted to infected
    hepatocytes. In the former, the infected mouse responded favorably, and in the manner of human
    patients, to a standard imunoglobulin therapy. In the latter, HCV-infected hepatocytes were
    successfully targeted for cell death, with repeated doses of Adenovirus-delivered BID being the
    most effective at inhibiting virus spread. Efficacy and toxic side-effects of BID treatment could
    be reconciled by modulating the timing between doses, the most effective tested being three doses
    of BID at 7-day intervals. Analyses of chimeric model production were undertaken to improve
    the quality of human hepatocyte engraftment (typically only 25-35% of mice receiving grafts are
    currently used experimentally). Minor variations in success rates were experienced with respect
    to donor age or health status, or the age of recipient mice within an operational window of 5 to 13
    days from birth. The greatest obstacle to useful engraftment (aside from technical challenges)
    was deemed to be the genetic/cellular integrity of the recipient mouse. This conclusion was
    based on variable engraftment success with ‘healthy’ donor cell preparations and a consideration
    of variability in immune deficiency arising in mice within a SCID/Bg mouse colony.

  • Subjects / Keywords
  • Graduation date
    Fall 2009
  • Type of Item
    Thesis
  • Degree
    Doctor of Philosophy
  • DOI
    https://doi.org/10.7939/R39S77
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.