Development of monoclonal catalytic antibodies for HIV immunotherapy

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$173,142.00
Award Year:
2010
Program:
STTR
Phase:
Phase I
Contract:
1R41AI087527-01
Award Id:
n/a
Agency Tracking Number:
R41AI087527
Solicitation Year:
2010
Solicitation Topic Code:
NIAID
Solicitation Number:
PA09-081
Small Business Information
MISSOURI CITY, TX, 77459-
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
830180282
Principal Investigator:
STEPHANIE PLANQUE
(713) 270-5391
stephanie.a.planque@uth.tmc.edu
Business Contact:
BENJAMIN ADLER
(713) 270-5391
benjamin.adler@mac.com
Research Institute:
University Of Texas Hlth Sci Ctr Houston

Box 20036
HOUSTON, TX, 77225-
() -
Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): We have raised murine monoclonal antibodies (MAbs) to a conserved region of the CD4 binding site of gp120 (CD4bs) that neutralize genetically diverse HIV strains. The MAbs have a novel mechanism of action. They hydrolyze multiple molecules of gp120, thereby imparting MAb increased biological efficacy. About 10% of HIV infected subjects develop resistance to currently available drug regimens and have no other treatment options. Our MAbs are intended to fulfill this unmetmedical need. In the present Phase I proposal, we will conduct molecular engineering and initial functional studies necessary to preparing therapy-grade MAbs. We will: (a) clone two chimeric MAbs (cMAbs) with reduced immunogenicity by fusing the murine catalytic variable domains to human IgG constant domains; (b) establish that the cMAbs express catalytic and epitope specificity properties comparable to the parent MAbs; (c) determine the potency with which the cMAbs neutralize genetically diverse HIV strains as the initial efficacy indicator; and (d) confirm the absence of cMAb cross-reaction with host human proteins, a requirement for a MAb designed for clinical use in humans. If the cMAbs meet the Phase I milestones, we will seek Phase II support for animal model efficacy tests, toxicity analysis and pharmacokinetic studies to enable human testing. PUBLIC HEALTH RELEVANCE: No adequate therapies are available for HIV infected patients who develop resistance to antiretroviral drugs. We will examine thefeasibility of developing antibodies that degrade the coat protein of HIV for treatment of such patients.

* information listed above is at the time of submission.

Agency Micro-sites


SBA logo

Department of Agriculture logo

Department of Commerce logo

Department of Defense logo

Department of Education logo

Department of Energy logo

Department of Health and Human Services logo

Department of Homeland Security logo

Department of Transportation logo

Enviromental Protection Agency logo

National Aeronautics and Space Administration logo

National Science Foundation logo
US Flag An Official Website of the United States Government