HIV infection is effectively controlled for many patients by long-term use of combination therapies that target actively replicating virus. However, currently available therapies do not lead to viral eradication and HIV remains an incurable, chronic condition. For many patients, substance abuse complicates the chronic administration of anti-retrovirals and predisposes to viralogic failure. Vulnerable patients who are unable to consistently use life-long, daily anti-retrovirals urgently need a cure. One promising strategy to eliminate latently infecting cells is ?shock and kill,? a strategy that depends on ?shocking? latent provirus to an active state so that it can be targeted effectively by medications or host immune factors. However, to effectively drug latently infected cells, we need a deeper understanding of the cellular factors that control viral latency. Functional testing of candidate host factors is critical to understand the mechanisms that control HIV latency. However functional genetic studies in primary human immune cells have been largely impossible until recently. We recently developed a robust CRISPR/Cas9-based technology that enables both `knock- out' and `knock-in' genome editing in primary human T cells. We now propose a comprehensive strategy to test how specific host factors control HIV latency in primary immune cells. The central innovation of this proposal is a high-throughput platform for rapidly generating isogenic human T cells with candidate factors deleted in an arrayed fashion. CRISPR/Cas9 ribonucleoproteins (RNPs) will be transiently delivered to T cells by electroporation to permanently delete targeted genes. This programmable platform will be exploited to rapidly identify and characterize human host factors that regulate multiple stages of the HIV lifecycle. We will focus on elucidating the key genes that control HIV latency and re-activation. Functional assessment of candidates will be performed using a novel HIV dual-fluorescence reporter that can differentiate between latently and productively infected primary T cells. The integration of genome-scale analysis and functional genetics in primary human T cells will accelerate the discovery of novel pathways that regulate HIV infection and latency. Importantly, we will validate the function of these novel regulators of latency using blood samples from HIV-infected patients with substance abuse. These studies are designed to develop targets for a new generation of HIV therapeutics aimed at eradicating latent virus from patients.

Public Health Relevance

A functional cure for HIV infection, which is urgently needed by patients whose chronic care is complicated by substance abuse, depends on improved understanding of the genetic factors that control viral latency in host cells. Progress has been limited by longstanding challenges in functional genetic testing in primary human immune cells, but we recently developed new tools to ?edit? specific DNA sequences in human T cells. We now propose to leverage this novel CRISPR/Cas9 genome-editing platform to identify, characterize and validate the function of latency factors in primary T cells, which could accelerate efforts to eradicate chronic HIV infection in patients suffering from substance abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
NIH Director’s New Innovator Awards (DP2)
Project #
1DP2DA042423-01
Application #
9180209
Study Section
Special Emphasis Panel (ZDA1-HXO-H (08)R)
Program Officer
Pollock, Jonathan D
Project Start
2016-06-01
Project End
2021-05-31
Budget Start
2016-06-01
Budget End
2021-05-31
Support Year
1
Fiscal Year
2016
Total Cost
$2,377,500
Indirect Cost
$877,500
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Hultquist, Judd F; Schumann, Kathrin; Woo, Jonathan M et al. (2016) A Cas9 Ribonucleoprotein Platform for Functional Genetic Studies of HIV-Host Interactions in Primary Human T Cells. Cell Rep 17:1438-1452