Development of AAV vectors for long-term expression of eCD4-Ig

NIH RePORTER · NIH · R44 · $999,443 · view on reporter.nih.gov ↗

Abstract

ABSTRACT / SUMMARY / PROJECT DESCRIPTION A single intramuscular injection of an adeno-associated virus (AAV) vector that expresses eCD4-Ig has the potential to treat or prevent HIV-1 infection for a lifetime. eCD4-Ig is a synthetic antibody or “immunoadhesin” constructed by fusing parts of the viral receptor (CD4) and coreceptor (CCR5) to the constant region of an antibody. Because eCD4-Ig binds the HIV-1 envelope glycoprotein (Env) through the same contacts used by Env to recognize its receptor and coreceptor, eCD4-Ig neutralizes 100% of HIV-1 isolates and presents fundamental barriers to viral escape. We have previously shown that rhesus macaques inoculated with AAV expressing eCD4-Ig exhibited sterilizing protection against high-dose intravenous challenges with simian- human immunodeficiency virus (SHIV). Now, we propose several practical innovations designed to maximize the concentrations of eCD4-Ig in plasma that are sustained over the long term by AAV-transduced muscle.

Key facts

NIH application ID
9979748
Project number
5R44AI134269-04
Recipient
EMMUNE, INC
Principal Investigator
MICHAEL DAVID ALPERT
Activity code
R44
Funding institute
NIH
Fiscal year
2020
Award amount
$999,443
Award type
5
Project period
2017-08-01 → 2021-07-31