Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Feb 24:6:22183.
doi: 10.1038/srep22183.

A curative regimen would decrease HIV prevalence but not HIV incidence unless targeted to an ART-naïve population

Affiliations

A curative regimen would decrease HIV prevalence but not HIV incidence unless targeted to an ART-naïve population

Dobromir T Dimitrov et al. Sci Rep. .

Abstract

HIV curative strategies currently under development aim to eradicate latent provirus, or prevent viral replication, progression to AIDS, and transmission. The impact of implementing curative programs on HIV epidemics has not been considered. We developed a mathematical model of heterosexual HIV transmission to evaluate the independent and synergistic impact of ART, HIV prevention interventions and cure on HIV prevalence and incidence. The basic reproduction number was calculated to study the potential for the epidemic to be eliminated. We explored scenarios with and without the assumption that patients enrolled into HIV cure programs need to be on antiretroviral treatment (ART). In our simulations, curative regimes had limited impact on HIV incidence if only ART patients were eligible for cure. Cure implementation had a significant impact on HIV incidence if ART-untreated patients were enrolled directly into cure programs. Concurrent HIV prevention programs moderately decreased the percent of ART treated or cured patients needed to achieve elimination. We project that widespread implementation of HIV cure would decrease HIV prevalence under all scenarios but would only lower rate of new infections if ART-untreated patients were targeted. Current efforts to identify untreated HIV patients will gain even further relevance upon availability of an HIV cure.

PubMed Disclaimer

Figures

Figure 1
Figure 1. ART and HIV prevention coverage drive decreases in epidemic potential if only ART treated patients are eligible for cure interventions.
(A) Values of the basic reproduction number (R0) assuming different annual treatment and cure rates assuming that enhanced HIV prevention is not available (k = 0). (B) Effects of HIV prevention coverage (k) on HIV eradication (curves represent R0 = 1). Under all scenarios, increasing annual cure rate has a negligible impact on R0.
Figure 2
Figure 2. ART coverage is the most critical factor driving decreased HIV incidence if cure is available to only ART treated patients.
Dynamics of HIV incidence measured as number of new HIV infections cases per 100 person years over 20 years for different combinations of HIV prevention coverage (k), ART initiation (τ) and cure (δ). Prevention programs are most effective at low treatment initiation rates per year.
Figure 3
Figure 3. ART coverage and annual cure rate drive decreases in HIV prevalence if cure is available to only ART treated patients.
Dynamics of HIV prevalence measured as percentage HIV infected in the population over 20 years for different combinations of HIV prevention coverage (k), ART initiation (τ) and cure (δ).
Figure 4
Figure 4. ART coverage, annual cure rate and HIV prevention coverage drive decreases in epidemic potential if ART untreated patients are recruited directly into cure programs.
(A) Values of the basic reproduction number (R0) assuming different annual treatment and cure rates assuming that enhanced HIV prevention is not available (k = 0). (B) Effects of HIV prevention coverage (k) on HIV eradication (curves represent R0 = 1).
Figure 5
Figure 5. ART and cure coverage drive decreased HIV incidence if ART untreated patients are recruited directly into cure programs.
Dynamics of HIV incidence measured as number of new HIV infections cases per 100 person years over 20 years for different combinations of HIV prevention coverage (k), ART initiation (τ) and cure (δ).
Figure 6
Figure 6. ART and cure coverage drive decreased HIV prevalence if ART untreated patients are recruited directly into cure programs.
Dynamics of HIV prevalence measured as percentage HIV infected in the population over 20 years for different combinations of HIV prevention coverage (k), ART initiation (τ) and cure (δ).

References

    1. Corey L. & Coombs R. W. The natural history of HIV infection: implications for the assessment of antiretroviral therapy. Clin Infect Dis 16 Suppl 1, S2–6 (1993). - PubMed
    1. Perelson A., Neumann A., Markowitz M., Leonard J. & Ho D. HIV-1 dynamics in vivo: virion clearance rate, infected cell life-span, and viral generation time. Science 271, 1582–1586 (1996). - PubMed
    1. The Antiretroviral Therapy Cohort Collaboration, Life expectancy of individuals on combination antiretroviral therapy in high-income countries: a collaborative analysis of 14 cohort studies. Lancet 372, 293–299 (2008). - PMC - PubMed
    1. Han Y. et al. Resting CD4+ T cells from human immunodeficiency virus type 1 (HIV-1)-infected individuals carry integrated HIV-1 genomes within actively transcribed host genes. J Virol 78, 6122–6133 (2004). - PMC - PubMed
    1. Hamlyn E. et al. Plasma HIV viral rebound following protocol-indicated cessation of ART commenced in primary and chronic HIV infection. PLoS ONE 7, e43754 (2012). - PMC - PubMed

Publication types

MeSH terms

Substances