Viral dynamics of of a latent HIV infection model with Beddington-DeAngelis incidence function, B-cell immune response and multiple delays

被引:8
作者
Wang, Yan [1 ]
Lu, Minmin [1 ]
Jiang, Daqing [1 ,2 ,3 ]
机构
[1] China Univ Petr East China, Coll Sci, Qingdao 266580, Peoples R China
[2] China Univ Petr East China, Key Lab Unconvent Oil & Gas Dev, Qingdao 266580, Peoples R China
[3] King Abdulaziz Univ, Fac Sci, Dept Math, Nonlinear Anal & Appl Math NAAM Res Grp, Jeddah 21589, Saudi Arabia
基金
中国国家自然科学基金;
关键词
latent infection; B-cell immune response; delay; Beddington-DeAngelis function; stability; Hopf bifurcation; VIRUS-TO-CELL; MATHEMATICAL-ANALYSIS; INTRACELLULAR DELAY; GLOBAL STABILITY; PERSISTENCE; RESERVOIR;
D O I
10.3934/mbe.2021014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this paper, an HIV infection model with latent infection, Beddington-DeAngelis infection function, B-cell immune response and four time delays is formulated. The well-posedness of the model solution is rigorously derived, and the basic reproduction number R-0 and the B-cell immune response reproduction number R-1 are also obtained. By analyzing the modulus of the characteristic equation and constructing suitable 1.yapunov functions, we establish the global asymptotic stability of the uninfected and the B-cell-inactivated equilibria for the four time delays, respectively. Hopf bifurcation occurs at the B-cell-activated equilibrium when the model includes the immune delay, and the B-cell-activated equilibrium is globally asymptotically stable if the model does not include it. Numerical simulations indicate that the increase of the latency delay, the cell infection delay and the virus maturation delay can cause the B-cell-activated equilibrium stabilize, while the increase of the immune delay can cause it destabilize.
引用
收藏
页码:274 / 299
页数:26
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