Technology ID
TAB-2750

Simple, Rapid, and Sensitive Real-Time PCR Assays for Detecting Drug Resistance of HIV

E-Numbers
E-198-2013-0
E-214-2013-0
E-511-2013-0
Lead Inventor
Johnson, Jeffrey (CDC)
Co-Inventors
Lipscomb, Jonathan (CDC)
Heneine, Walid (CDC)
Applications
Therapeutics
Software / Apps
Research Materials
Occupational Safety and Health
Diagnostics
Consumer Products
Therapeutic Areas
Ophthalmology
Oncology
Infectious Disease
Endocrinology
Dental
Cardiology
Development Stages
Pre-Clinical (in vitro)
Development Status
In vitro data available
Research Products
Computational models/software
Lead IC
CDC
ICs
CDC
This novel assay features real-time PCR reagents and methods for detecting drug-resistance related mutations in HIV, for newly diagnosed patients and those individuals currently receiving antiretroviral therapies. As the use of antiretroviral compounds to treat HIV infection proliferates, viruses adapt and evolve mutations limiting the efficacy of these drugs and disrupting the success of treatment. To address this problem, CDC researchers have developed this RT-PCR assay, intended for diagnosis of different point mutations in patient samples at an achievable sensitivity of 1-2 log greater than conventional point-mutation sequencing methods. More specifically, this assay measures the differential amplifications of common and mutation-specific reactions that target specific codons of interest. Given its low cost, simplicity, high-throughput capability, and tremendous diagnostic sensitivity, this assay will be useful for detection and surveillance of drug resistance-associated mutations and will aid in the clinical management of HIV infection.
Commercial Applications
  • Clinical management of HIV infected patients
  • Pre-treatment evaluation baseline HIV infection to tailor appropriate drug combinations
  • Monitor the spread of resistant viruses
  • Blood donation screening
  • Research tool to study emergence and biology of drug resistance mutations
Competitive Advantages
  • Cost-effective
  • Sensitive and rapid
  • Capable of resistance mutation detection in both subtype B and non-B subtypes of HIV -1, and in HIV-2
  • Easily formatted for use in kits
  • High-throughput capable
Licensing Contact:
Mitzelfelt, Jeremiah
jeremiah.mitzelfelt@nih.gov