A COMPARISON OF DETERMINISTIC AND STOCHASTIC MODEL ON THE DYNAMICS OF HIV AND CD4+ T-CELLS INTERACTIONS

被引:0
|
作者
Mutiara, Alfiandhani Suci [1 ]
Kasbawati [1 ]
Jaya, Andi Kresna [2 ]
Anisa [2 ]
Samsir, Rusni [1 ]
机构
[1] Hasanuddin Univ, Fac Math & Nat Sci, Dept Math, Makassar, Indonesia
[2] Hasanuddin Univ, Fac Math & Nat Sci, Dept Stat, Makassar, Indonesia
关键词
HIV; HAART; stochastic and deterministic models; non-negativity solution; Euler Maruyama method; HUMAN-IMMUNODEFICIENCY-VIRUS; QUALITY-OF-LIFE; ANTIRETROVIRAL THERAPY; DRUG-RESISTANCE; COMBINATION; INFECTION; HAART; MORTALITY; OPTIMIZATION; ZIDOVUDINE;
D O I
10.28919/cmbn/7147
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
This study aims to present a comparison of deterministic and stochastic approaches on the interaction of HIV and CD4(+) T-cells with effects of HAART treatment. A three-dimensional nonlinear model is formulated with randomness that is considered as a Brownian motion coming from the uncertainty of the death rate of cells and viruses. We establish sufficient conditions for stability of endemic and nonendemic solutions that associate with an early reproductive threshold value of HIV infection which is linearly negative depending on the HAART treatment parameters. Non-negative stochastic solutions are also analysed. Numerical simulations show that HAART parameters have a significant effect in reducing HIV infection. The smaller value of treatment parameter, the more infected cells, which is also indicated by a threshold value that is greater than one. It also results in high fluctuations in the stochastic solutions. If the treatment parameter increases due to regular treatment, the number of infected cells and viruses decreases. It also reduces high fluctuations in the stochastic solutions which on average follow the decreasing trend of deterministic solutions. These results provide an overview of the intervals of the number of viruses and infected cells produced before and after being given treatment.
引用
收藏
页数:25
相关论文
共 50 条
  • [31] Development of a primary cell model of HIV-1 latency in naive CD4+ T-cells
    Zerbato, J.
    Sluis-Cremer, N.
    ANTIVIRAL THERAPY, 2013, 18 : A25 - A25
  • [32] CD8+ T-CELLS INHIBIT HIV REPLICATION IN NATURALLY INFECTED CD4+ T-CELLS - EVIDENCE FOR A SOLUBLE INHIBITOR
    BRINCHMANN, JE
    GAUDERNACK, G
    VARTDAL, F
    JOURNAL OF IMMUNOLOGY, 1990, 144 (08): : 2961 - 2966
  • [33] Stability analysis for a fractional differential model of HIV infection of CD4+ T-cells with time delay
    Yan, Ye
    Kou, Chunhai
    MATHEMATICS AND COMPUTERS IN SIMULATION, 2012, 82 (09) : 1572 - 1585
  • [34] Use of dendritic cells and CD4+ T-cells to expand γδ T-cells for immunotherapy
    Ye, Z
    Rich, IN
    Lamb, LS
    Harris, WG
    Lee, C
    Gee, AP
    Henslee-Downey, PJ
    EXPERIMENTAL HEMATOLOGY, 1998, 26 (08) : 743 - 743
  • [35] A mathematical model for transmission dynamics of HIV/AIDS with effect of weak CD4+ T cells
    Dutta, Ajoy
    Gupta, Praveen Kumar
    CHINESE JOURNAL OF PHYSICS, 2018, 56 (03) : 1045 - 1056
  • [36] Stability of discrete-time HIV dynamics models with three categories of infected CD4+ T-cells
    A. M. Elaiw
    M. A. Alshaikh
    Advances in Difference Equations, 2019
  • [37] Stability of discrete-time HIV dynamics models with three categories of infected CD4+ T-cells
    Elaiw, A. M.
    Alshaikh, M. A.
    ADVANCES IN DIFFERENCE EQUATIONS, 2019, 2019 (01)
  • [38] On the numerical solution of the model for HIV infection of CD4+ T cells
    Merdan, Mehmet
    Gokdogan, Ahmet
    Yildirim, Ahmet
    COMPUTERS & MATHEMATICS WITH APPLICATIONS, 2011, 62 (01) : 118 - 123
  • [39] REDUCED CD4+ T-CELLS AND SEVERE ORAL CANDIDIASIS IN ABSENCE OF HIV INFECTION
    PANKHURST, C
    PEAKMAN, M
    LANCET, 1989, 1 (8639): : 672 - 672
  • [40] HIV-1 ASSOCIATED SUPERANTIGEN (SA) - EFFECT ON CD4+ T-CELLS
    POSNETT, DN
    HODTSEV, AS
    ASCH, A
    LAURENCE, J
    CLINICAL RESEARCH, 1992, 40 (02): : A332 - A332