Partnership Opportunities

Point-of-Treatment Assays to Direct HIV Treatment

Developing simple, rapid methods for determining drug resistance and viral persistence

Technology Overview

Lisa FrenkelDr. Lisa FrenkelDr. Frenkel's group does basic, clinical, and translational research on mechanisms of HIV persistence and HIV drug resistance. This work is the basis for a rapid, point-of-treatment, oligonucleotide ligation assay (OLA) being developed in conjunction with scientists and engineers from the University of Washington. Their assay will detect if a patient with HIV has viruses resistant to treatment with World Health Organization defined “first-line antiretroviral therapy (ART), or if a patient acquires drug-resistance viruses during treatment or pre-exposure prophylaxis.

ART has revolutionized HIV treatment, but studies by Dr. Frenkel and others show that the prevalence of viral drug resistance, even before treatment, is increasing. A simple test for pretreatment drug resistance could help clinics, particularly in resource-limited areas, by ensuring that patients will benefit from standard “first-line” ART. The test could help patients with drug-resistant HIV by directing their health care providers to prescribe other therapies that will be effective for their HIV.

The basis for OLA is Dr. Frenkel’s research that identified single-nucleotide polymorphisms (SNPs) in the HIV genome that, if detected prior to ART, confer viral resistance and are associated with therapeutic failure. Patients infected by HIV with these point mutations are not expected to respond to first-line ART. And if a patient’s treatment stops working due to intermittent treatment, these mutations are selected.

OLA is a multiplexed test that detects the HIV SNPs associated with ART treatment failure. To perform the assay, the viral nucleic acids from a patient sample are amplified, followed by addition of oligonucleotide probes. If the probes are perfectly complementary to the viral DNA at the SNP and two adjacent nucleotides the probes will be covalently ligated to each other, which generates a fluorescence-based or other visual signal.

Dr. Frenkel’s group successfully field-tested OLA in a randomized trial onsite in a clinical laboratory in Kenya. The trial showed that OLA can be implemented in a resource-limited setting and improve the clinical outcome of individuals who entered the study with drug-resistant viruses.

Dr. Frenkel is interested in partnerships to further develop OLA. Examples of advancements in OLA include generating rapid, paper-strip OLA for multiplexed detection of ART-resistant HIV strains. Providing the assays in simple kits could promote their implementation in areas with limited resources. Dr. Frenkel is also working on V-OLA, a rapid point-of-care assay to monitor viral load and test for HIV drug-resistance mutations.

Stage of Development

  • Pre-clinical ex vivo
  • Clinical trials

Partnering Opportunities

  • Collaborative research opportunity
  • Sponsored research agreement
  • Consultation agreement
  • Tissue sample access
  • Kit development

Publications

  1. Beck IA, Levine M, McGrath CJ, Bii S, Milne RS...Frenkel LMPre-treatment HIV-drug resistance associated with virologic outcome of first-line NNRTI-antiretroviral therapy: A cohort study in Kenya. EClinicalMedicine. 2020 Jan 14;18:100239. doi: 10.1016/j.eclinm.2019.100239. eCollection 2020 Jan.  PMID:  31956856
  2. Panpradist N, Beck IA, Vrana J, Higa N, McIntyre D...Frenkel LM, Lutz BR. OLA-Simple: A software-guided HIV-1 drug resistance test for low-resource laboratories.  EBioMedicine. 2019 Dec;50:34-44. doi: 10.1016/j.ebiom.2019.11.002. Epub 2019 Nov 22.
  3. Chung MH, McGrath CJ, Beck IA, Levine M, Milne RS...Frenkel LMEvaluation of the management of pretreatment HIV drug resistance by oligonucleotide ligation assay: a randomised controlled trial.  Lancet HIV. 2019 Dec 6. pii: S2352-3018(19)30337-6. doi: 10.1016/S2352-3018(19)30337-6.
  4. Milne RS, Silverman RA, Beck IA, Mckernan-Mullin J, Deng W, Sibley TR...Frenkel LM. Minority and majority pretreatment HIV-1 drug resistance associated with failure of first-line nonnucleoside reverse-transcriptase inhibitor antiretroviral therapy in Kenyan women. AIDS. 2019;33(6):941-951.
  5. Duarte HA, Beck IA, Levine M, Kiptinness C, Kingoo JM, Chohan B. Sakr SR, Chung MH, Frenkel LM. Implementation of a point mutation assay for HIV drug resistance testing in Kenya. AIDS. 2018;32(16):2301-2308. doi: 10.1097/QAD.0000000000001934.
  6. Beck IA, Deng W, Payant R, Hall R, Bumgarner RE, Mullins JI, Frenkel LM. Validation of an oligonucleotide ligation assay for quantification of human immunodeficiency virus type 1 drug-resistant mutants by use of massively parallel sequencing. J Clin Microbiol. 2014;52(7):2320-7. doi: 10.1128/JCM.00306-14.
  7. Jourdain G, Wagner TA, Ngo-Giang-Huong N, Sirirungsi W, Klinbuayaem V...Frenkel LM, Lallemant M. Association between detection of HIV-1 DNA resistance mutations by a sensitive assay at initiation of antiretroviral therapy and virologic failure. Clin Infect Dis. 2010; 50:1397-1404.

Learn More

To learn more about partnering with Seattle Children’s Research Institute on this or other projects, please contact:

Dr. Elizabeth Aylward, Director 
Office of Science-Industry Partnerships 
Seattle Children’s Research Institute 
818 Stewart Street, Suite 603
Seattle, WA 98101
Email
206-884-1065