AAV-vectored immunoprophylaxis for the prevention and treatment of infectious diseases

  • Funded by Canadian Institutes of Health Research (CIHR)
  • Total publications:0 publications

Grant number: 456332

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Key facts

  • Disease

    Disease X
  • start year

    2021
  • Known Financial Commitments (USD)

    $78,858.79
  • Funder

    Canadian Institutes of Health Research (CIHR)
  • Principal Investigator

    Wootton Sarah
  • Research Location

    Canada
  • Lead Research Institution

    Avamab Pharma Inc. (Calgary, Alberta)
  • Research Priority Alignment

    N/A
  • Research Category

    Therapeutics research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Adeno-associated virus (AAV)-mediated expression of pathogen specific, broadly protective monoclonal antibodies (mAb) has been demonstrated to provide protection against a variety of infectious diseases in a range of animal models and is now being tested in two human clinical trials for human immunodeficiency virus (HIV) (NCT03374202 and NCT01937455). Our patented (U.S. patent US 10,806,802) AAV-mAb expression platform utilizes a novel, rationally engineered AAV6 mutant capsid, termed AAV6.2FF, which has been shown to be highly efficacious as a prophylactic against Ebola virus and C. Difficile toxin challenge, among other infectious diseases. In this proposal we aim to optimize and expand our vectored immunoprophylaxis (VIP) platform to aid in the clinical translation of this promising alternative vaccine and therapeutic strategy. Specifically, we will investigate AAV-vectored mAb expression kinetics, anti-drug antibody development, effect of pre-existing immunity, and ways to modulate gene expression and in a range of larger animal models including guinea pigs, ferrets, sheep, and non-human primates. Finally, we will implement novel vector design improvements and explore new applications for AAV-vectored mAb expression.