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High Throughput In Vitro Assessment of Latency Reversing Agents on HIV Transcription and Splicing
Published on: January 22, 2019
Stability of HTLV/HIV dual infection model with mitosis and latency
A M Elaiw1,2, N H AlShamrani1,3
1Department of Mathematics, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia.
Abstract:
In this paper, we formulate and analyze an HTLV/HIV dual infection model taking into consideration the response of Cytotoxic T lymphocytes (CTLs). The model includes eight compartments, uninfected CD4+T cells, latent HIV-infected cells, active HIV-infected cells, free HIV particles, HIV-specific CTLs, latent HTLV-infected cells, active HTLV-infected cells and HTLV-specific CTLs. The HIV can enter and infect an uninfected CD4+T cell by two ways, free-to-cell and infected-to-cell. Infected-to-cell spread of HIV occurs when uninfected CD4+T cells are touched with active or latent HIV-infected cells. In contrast, there are two modes for HTLV-I transmission, (ⅰ) horizontal, via direct infected-to-cell touch, and (ⅱ) vertical, by mitotic division of active HTLV-infected cells. We analyze the model by proving the nonnegativity and boundedness of the solutions, calculating all possible steady states, deriving a set of key threshold parameters, and proving the global stability of all steady states. The global asymptotic stability of all steady states is proven by using Lyapunov-LaSalle asymptotic stability theorem. We performed numerical simulations to support and illustrate the theoretical results. In addition, we compared between the dynamics of single and dual infections.
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