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. 2021 Jul 29;11(8):766. doi: 10.3390/life11080766

Threshold Dynamics of a Non-Linear Stochastic Viral Model with Time Delay and CTL Responsiveness

Jianguo Sun 1,*, Miaomiao Gao 1, Daqing Jiang 1,2
Editors: Tao Huang, Koichiro Tamura
PMCID: PMC8399283  PMID: 34440510

Abstract

This article focuses on a stochastic viral model with distributed delay and CTL responsiveness. It is shown that the viral disease will be extinct if the stochastic reproductive ratio is less than one. However, when the stochastic reproductive ratio is more than one, the viral infection system consists of an ergodic stationary distribution. Furthermore, we obtain the existence and uniqueness of the global positive solution by constructing a suitable Lyapunov function. Finally, we illustrate our results by numerical simulation.

Keywords: stochastic viral model, time delayed, CTL responsiveness, ergodic stationary distribution, extinction

1. Introduction

It is confirmed that approximately 100–250 million people are infected every year by different viruses, especially in regions of Asia and Africa [1]. To control epidemic viral diseases, an epidemic viral model is very useful, which can provide insights into the dynamics of viruses in vivo and offer a better understanding of viral diseases [2,3,4,5,6,7,8,9,10].

CTLs (Cytotoxic T Lymphocytes) play a significant role in antiviral mechanisms. On the one hand, CTLs imply the main immune factor inhibiting cell that limits the development of virus replication in vivo and depends on viral load [11,12,13]; on the other hand, it has recently been demonstrated that infected cells are killed not by the virus but by specific CTLs in some infectious diseases such as hepatitis B [3,14]. Therefore, the dynamics of the epidemic viral model with CTL responsiveness have drawn much attention from researchers in related areas [11,12,13,14,15,16].

The CTL immune response against a single pool of infected viral cells has been considered in [15,16,17], which is described by the following system:

dx(t)=(λ−hx−exy)dt,dy(t)=(exy−ay−pyz)dt,dz(t)=(f(y,z)−bz)dt, (1)

where the definitions of the variables are described in the following Table 1.

Table 1.

Variables in the model (adapted from [15,16]).

Variables Definition
x(t) the number of susceptible host cells at time t
y(t) the virus population at time t
z(t) the number of CTLs at time t
λ susceptible host cells generation rate
hx susceptible host cells death rate
exy rate at which susceptible host cells become infected by the virus
ay infected cells death rate
pyz rate at which infected cells are killed by the CTL
f(y,z) rate of immune response due to virus activation

Note that time-series data of the immune state of patients look rather irregular. The possibility of dynamics of infinite delay has been introduced into the equations used in mathematical biology models since Volterra [18,19,20,21,22] translated the cumulative effect of the history of a system. K. Wang et al. [13] incorporate a time delay of the immune response in the system (1) to obtain the following system:

dx(t)=(λ−hx(t)−ex(t)y(t))dt,dy(t)=(ex(t)y(t)−ay(t)−py(t)z(t))dt,dz(t)=(cy(t−τ)−bz(t))dt, (2)

They described the relationship between virus replication and the instantaneous immune response.

In the real world, epidemic models are also affected by escapable environmental white noise [5,6,7,8,9,23,24,25,26,27,28], full of randomness and stochasticity. As we understand it, there is little to no work researching the extinction and the ergodic stationary distribution of a system (2) with stochasticity and distributed delay, which is mainly due to the fact that Equation (2) is of a degenerate type. In this paper, we use an asymptotic approach [6,8,9,25] and give the following system:

dx(t)=(λ−hx(t)−ex(t)y(t))dt−σ1xdB1(t),dy(t)=(ex(t)y(t)−ay(t)−py(t)z(t))dt−σ2ydB2(t),dz(t)=(cw(t)−bz(t))dt−σ3zdB3(t),dw(t)=σ(y(t)−w(t))dt, (3)

The main purpose of this paper is to study the ergodic stationary distribution and extinction of the system (3). The existence and uniqueness of the global positive solution are also introduced.

The remainder of the paper is organized as follows. In Section 2, we introduce some necessary results throughout this paper. In Section 3, we show the uniqueness and positivity of global positive solutions of a stochastic system (3) with any positive initial value. In Section 4, we prove the existence and uniqueness of an ergodic stationary distribution of the solutions to the system (3) by constructing a suitable stochastic Lyapunov function; furthermore, we establish the persistence in the mean of the solutions of the system (3). In Section 5, we establish sufficient conditions for the extinction of the viral model. Some numerical simulations are introduced to demonstrate the theoretical results and reveal the effects of white noise. Finally, some concluding remarks and future directions are presented to close this paper.

2. Preliminaries

Throughout this paper, we first give some basic conceptions, as in [6]. Let (Ω,F,{Ft}t≥0,P) be a complete probability space with a filtration {Ft}t≥0 satisfying the usual conditions (i.e., it is right continuous, and F0 contains all P−null sets). Define R+4={x∈R4:xi>0forall1≤i≤4}, R¯+4={x∈R4:xi≥0forall1≤i≤4}. In addition, if g(t) is an integral function on t∈[0,∞), define gμ=sup{g(t)∣t≥0},gl=inf{g(t)∣t≥0}.

Firstly, we consider the general 4-dimensional stochastic differential equation

dx(t)=l(x(t),t)dt+q(x(t),t)dB(t),fort≥t0 (4)

with initial value x(t0)=x0∈R4, where B(t) denotes 4-dimensional standard Brownian motion defined on the above probability space. Define the differential operator L associated with Equation (4) by Mao [6] as

L=∂∂t+Σli(x,t)∂∂xi+12Σ[qT(x,t)q(x,t)]ij∂2∂xi∂xj.

If L acts on a function V∈C2,1(R4×R¯+;R¯+), then

LV(x,t)=Vt(x,t)+Vx(x,t)+12trac[qT(x,t)Vxx(x,t)q(x,t)],

where Vt=∂V∂t,Vx=(∂V∂x1,…,∂V∂x4) and Vxx=(∂2V∂xi∂xj)4×4. Let x(t) be a homogeneous Markov process in R4, which is described as the following stochastic differential equation by Ito^′s formula [6]:

dV(x(t),t)=LV(x(t),t)dt+Vx(x(t),t)r(x(t),t)dB(t).

The diffusion matrix is defined as follows:

A(x)=(aij(x)),aij=∑r=14gri(x)grj(x).

3. Existence and Uniqueness of the Global Positive Solution

To study the dynamical behaviors of a viral model, where the solution is global and positive, because the coefficients of the system (3) do not satisfy the linear growth, the solutions of the system (3) may explode at a finite time. In this section, we show that there is a unique global positive solution of the system (3) from the idea in [8], the main theorem as follows.

Theorem 1.

For any initial value (x(0),y(0),z(0),w(0))∈R+4, there is a unique positive solution (x(t),y(t),z(t),w(t)) of system (3) on t≥0, and the solution will remain in R+4 with a probability of one; that is to say, (x(t),y(t),z(t),w(t))∈R+4 for all t≥0, almost surely.

Proof. 

Our proof is based on the works of Mao et al. [9]. We know the coefficients of system (3) are locally Lipschitz continuous; thus, there is a unique solution (x(t),y(t),z(t),w(t)) on [0,τ0) for any initial value (x(0),y(0),z(0),w(0))∈R+4, where τ0 is an explosion time. If τ0=∞ a.s, we can determine that the local solution is global. Let n0 be a sufficiently large positive number for every component of (x(0),y(0),z(0),w(0)) lying in [1n0,n0]; for any n≥n0, the stopping time

τn=inf{t∈[0,τ0):min{x(t),y(t),z(t),w(t)}≤1normax{x(t),y(t),z(t),w(t)}≥n}. (5)

We set infϕ=∞. Obviously, τn is increasing as n→∞. Set τ∞=limn→∞τn; thus, τ∞≤τ0 a.s. If we can prove that τ∞=∞ a. s., then τ0=∞, which implies (x(t),y(t),z(t),w(t))∈R+4 a. s. for all t≥0. If τ∞<∞ a.s., it is the same. If we want to complete the proof, we should verify that τ∞=∞ a. s. If this assertion is false, there are two constants T≥0 and ε∈(0,1), such that

P{τ∞≤T}≥ε.

In addition, there is an integer n1≥n0, such that

P{τn≤T}≥εforalln≥n1.

We define a fundamental C2-function U:R+4→R¯+, which is

U=(x(t)−α−αlnx(t)α)+(y(t)−β−βlny(t)β)+(z(t)−1−lnz(t))+γ(w(t)−1−lnw(t)), (6)

where α,β,γ are positive constants, which will be determined in the following text. The non-negativity of the function U can be seen from x−1−lnx≥0 for any x>0.

Applying Ito^′s formula [6], we obtain

dU(x,y,z,w)=LUdt−σ1(x(t)−α)dB1(t)−σ2(y(t)−β)dB2(t)−σ3(z(t)−1)dB3(t), (7)

where

LU(x,y,z,w)=(1−αx)dx+(1−βy)dy+(1−1z)dz+γ(1−1w)dw+12(ασ12+βσ22+σ32=λ−dx−exy−αλx+dα+αey+exy−ay−pyz−βex+βa+βpz+cw−bz−cwz+b+γσy−γσw−γσyw+γσ+12(ασ12+βσ22+σ32. (8)

Choosing

α=a−ce,β=bp,γ=cσ,

such that αe+γσ=a,βp=b,γσ=c, we can then obtain

LU(x,y,z,w)≤λ+ad+βa+b+γσ≤λ+ad+abp+b+c+12(a−ceσ12+bpσ22+σ32):=K, (9)

where K is a positive constant. The remainder of the proof is similar to Theorem 3.1 in Mao [9]. Hence, we omit it here. □

4. Ergodic Stationary Distribution

Here, we present some theories about the stationary distribution in this section. Although there is no endemic equilibrium point of the stochastic system (3), we want to obtain the existence of an ergodic stationary distribution, which indicates the persistence of the disease. Firstly, we define R0* as a stochastic reproductive ratio of the system (3), such as

R0*=λea(a+12σ22)2(d+12σ12),

which is equal to R0=λead when σ1=σ2=0 [13]. Some known results about the theory of Has’Minskii are found in [28].

Lemma 1

([28]). The Markov process X(t) has a unique ergodic stationary distribution μ(·) if there exists a bounded domain U⊂El with regular boundary Γ, and

  • (A.1)

    there is a positive number M such that ∑i,j=1laij(x)ξiξj≥M|ξ|2,x∈U,ξ∈Rl.

  • (A.2)
    there exists a non-negative C2 function V, such that LV is negative for any El\U. Then,
    PxlimT→∞1T∫0Tf(X(t))dt=∫Elf(x)μ(dx)=1,
    for all x∈El, where f(·) is a function integrable with respect to the measure μ.

Based on the theory of Has’minskii [28], we will give conditions which guarantee the existence of an ergodic stationary distribution.

Theorem 2.

Assume that R0*>1, then the solution (x(t),y(t),z(t),w(t)) of system (3) has an ergodic unique stationary distribution for any initial value (x(0),y(0),z(0),w(0))∈R+4.

Proof. 

The proof of Theorem 2 should satisfy the conditions of Lemma 1. Verify that (A.1) holds. Apparently, the corresponding diffusion matrix of system (3) is given by

A=σ12x20000σ22y20000σ32z20000w2.

Choosing M˜=min(x,y,z,w)∈Dε{σ12x2,σ22y2,σ32z2,w2}>0, we obtain

∑i,j=14aij(x,y,z,w)ξiξj=σ12x2ξ12+σ22y2ξ22+σ32z2ξ32+w2ξ42≥M˜∣ξ∣2,

for all (x,y,z,w)∈Dε,ξ=(ξ1,ξ2,ξ3,ξ4)∈R+4, where

Dε={(x,y,z,w)∈R+4:ε<x<1ε,ε<y<1ε,ε<z<1ε,ε<w<1ε}

is a bounded closed set, and ε>0 is a sufficiently small number. Thus, condition (A.1) is completed.

Now, we construct a C2-function V:R+4→R as follows:

V(x,y,z,w)=M(−lnx−c0lny)−c1lny−lnz−lnw+1θ+1(x+y+a4cz+a2σw)θ+1,

where θ∈(0,minaa+σ22,bb+σ32,dd+σ12) is a positive constant, and c1≤−2+b+σ+12(σ22+σ32)a.

When R0*>1, the constant M satisfies the following condition:

0<M≤−2(d+12σ12)(1−R0*).

Applying Ito^′s formula to the function V(x,y,z,w), denote

V1=−lnx−c0lny,V2=−c1lny,
V3=−lnz,V4=−lnw,
V5=1θ+1(x+y+a4cz+a2σw)θ+1.

We can apply the differential operator L to the above functions, respectively,

LV1=−1xx′−c01yy′+12(σ12+c0σ22)=−λx+d+ey−c0ex+c0a+c0pz+12(σ12+c0σ22)≤−2λc0e+c0a+12c0σ22+d+12σ12+ey+c0pz. (10)

Supposing

g(c0)=−2λc0e+c0a+12c0σ22,
g′(c0)=−λeλc0e+a+12σ22=0,

we can obtain

c0=λe(a+12σ22)2.

Hence,

LV1=g(c0)+d+12σ12+ey+c0pz≤−λea(a+12σ22)2+d+12σ12+ey+c0pz=(d+12σ12)(1−λea(a+12σ22)2(d+12σ12))+ey+λep(a+12σ22)2z=(d+12σ12)(1−R0*)+ey+λep(a+12σ22)2z; (11)
LV2=−c11yy′+12σ12=−c1ex+c1a+c1pz+12σ22; (12)
LV3=−1zz′+12σ32=−cwz+b+12σ32; (13)
LV4=−1ww′=−σyw+b+σ; (14)
LV5=(x+y+a4cz+a2σw)θ(x′+y′+a4cz′+a2σw′)+θ2(x+y+a4cz+a2σw)θ−1(σ12x2+σ22y2+(a4c)2σ32z2)≤(x+y+a4cz+a2σw)θ(λ−dx−a2y−a4w−ab4cz)+θ2(x+y+a4cz+a2σw)θ−1(σ12x2+σ22y2+(a4c)2σ32z2)≤λ(x+y+a4cz+a2σw)θ−(dx+a2y+ab4cz+a4w)(xθ+yθ+(a4c)θzθ+(a2σ)θwθ)+θ2(x+y+a4cz+a2σw)θ−1(σ12x2+σ22y2+(a4c)2σ32z2)≤λ(x+y+a4cz+a2σw)θ−dxθ+1−a2yθ+1−(a4c)θ+1bzθ+1−a4(a2σ)θwθ+1+θ2(x+y+a4cz+a2σw)θ−1(σ12x2+σ22y2+(a4c)2σ32z2)≤B−dθxθ+1−a2θyθ+1−(a4c)θ+1bθzθ+1−aθ+12θ+3σθwθ+1, (15)

where

B=sup{λ(x+y+a4cz+a2σw)θ+θ2(x+y+a4cz+a2σw)θ−1(σ12x2+σ22y2+(a4c)2σ32z2),−d(1−θ)xθ+1−a2(1−θ)yθ+1−(a4c)θ+1b(1−θ)zθ+1−aθ+12θ+4σθwθ+1},

where θ∈(0,minaa+σ22,bb+σ32,dd+σ12) is a positive constant, and B<0. From the above analysis, we have

LV(x,y,z,w)=MLV1+LV2+LV3+LV4+LV5≤M((d+12σ12)(1−λea(a+12σ22)2(d+12σ12))+ey+λep(a+12σ22)2z)−c1ex+c1a+c1pz+12σ22−1zz′+12σ32=−cwz+b+12σ32−1ww′=−σyw+b+σ+B−dθxθ+1−a2θyθ+1−(a4c)θ+1bθzθ+1−aθ+12θ+3σθwθ+1, (16)

and we define

f1(x)=c1a+b+σ+12(σ22+σ32)−c1ex−dθxθ+1,
f2(y)=M((d+12σ12)(1−λea(a+12σ22)2(d+12σ12))+ey)−a2θyθ+1,
f3(z)=Mλep(a+12σ22)2z+c1pz−cwz−(a4c)θ+1bθzθ+1,
f3(w)=B−σyw−aθ+12θ+3σθwθ+1.

We can divide R+4\Dε into the following eight domains:

D1={(x,y,z,w)∈R+4:0<x<ε};D2={(x,y,z,w)∈R+4:0<y<ε};
D3={(x,y,z,w)∈R+4:0<z<ε,ε<w<1ε};D4={(x,y,z,w)∈R+4:ε<z<1ε,0<w<ε};
D5={(x,y,z,w)∈R+4:x>1ε};D6={(x,y,z,w)∈R+4:y>1ε};
D7={(x,y,z,w)∈R+4:z>1ε};D8={(x,y,z,w)∈R+4:w>1ε}.

Clearly, Dε=⋃j=18Dj. In the following text, we will show that LV(x,y,z,w)≤−1 on R+4\Dε, which is equivalent to prove it on the above eight domains.

Case 1. If (x,y,z,w)∈D1, one can choose

c1≤−2+b+σ+12(σ22+σ32)a,

and

LV(x,y,z,w)≤c1a+b+σ+12(σ22+σ32)−c1ex−dθxθ+1≤−2;

Case 2. If (x,y,z,w)∈D2, one can choose R0*>1 and

0<M≤−2(d+12σ12)(1−R0*),
LV(x,y,z,w)≤M((d+12σ12)(1−R0*)+ey)−a2θyθ+1≤−2;

Case 3. If (x,y,z,w)∈D3,

LV(x,y,z,w)≤Mλep(a+12σ22)2z+c1pz−cwz−(a4c)θ+1bθzθ+1≤−cwz≤−2;

Case 4. If (x,y,z,w)∈D4,

LV(x,y,z,w)≤B−σyw−aθ+12θ+3σθwθ+1≤−σyw≤−2;

Case 5. If (x,y,z,w)∈D5,

LV(x,y,z,w)≤c1a+b+σ+12(σ22+σ32)−c1ex−dθxθ+1≤−c1ex−dθxθ+1≤−2;

Case 6. If (x,y,z,w)∈D6,

LV(x,y,z,w)≤M((d+12σ12)(1−R0*)+ey)−a2θyθ+1≤M((d+12σ12)(1−R0*)+ey)−a2θ(1ε)θ+1≤−2; (17)

Case 7. If (x,y,z,w)∈D7, because Mλep(a+12σ22)2+c1p−(a4c)θ+1bθ(1ε)θ<0, we determine that

LV(x,y,z,w)≤Mλep(a+12σ22)2z+c1pz−cwz−(a4c)θ+1bθzθ+1≤z(Mλep(a+12σ22)2+c1p)−cwε−(a4c)θ+1bθzθ+1≤z(Mλep(a+12σ22)2+c1p−(a4c)θ+1bθ(1ε)θ)≤−1ε≤−2; (18)

Case 8. If (x,y,z,w)∈D8, because B<0, we determine that

LV(x,y,z,w)≤B−σyw−aθ+12θ+3σθwθ+1≤B−aθ+12θ+3σθ(1ε)θ+1≤−2.

Therefore, for all (x,y,z,w)∈R+4\Dε, V(x,y,z,w)≤−1, which indicates that assumption (A.2) holds.

We can know that the system (3) is ergodic and has a unique stationary distribution. This completes the proof. □

5. Extinction of the System 3

For the dynamical behavior of epidemic viral models, the main concern is finding the condition in which the virus will be eradicated in a long time when R0*>1. In this section, we shall consider the extinction of the system (3).

According to the results in [9], we can obtain the following lemma.

Lemma 2.

For any initial value, the solution of the stochastic model satisfies

limt→∞lnx(t)t≤0,limt→∞lny(t)t≤0,limt→∞lnz(t)t≤0,limt→∞lnw(t)t≤0a.s. (19)
limt→∞x(t)+y(t)+z(t)+w(t)t=0,a.s.. (20)

Moreover,

limt→01t∫0tx(m)dB1(m)=0,limt→01t∫0ty(m)dB2(m)=0,limt→01t∫0tz(m)dB3(m)=0a.s.. (21)

Theorem 3.

Let (x,y,z,w) be the solution of system (3) with any initial value (x(0),y(0),z(0),w(0))∈R+4. If R0*<1, then the solution (x,y,z,w) of system (3) satisfies

lim supt→∞lny(t)t≤(a+12σ22)(R0*−1)<0a.s..

Namely, the disease will be eradicated in the long term.

Proof. 

Applying Itô’s formula to lny(t), we obtain

dlny(t)=(ex−a−pz−12σ22)dt+σ2dB2(t)≤[ex−(a+12σ22)]dt+σ2dB2(t). (22)

Integrating the above formula from 0 to t on both sides, then

lny(t)−lny(0)≤∫0t[ex−(a+12σ22)]ds+∫0tσ2dB2(s).

According to the strong law of large numbers [29], we have

limt→01t∫0tdB2(s)=0a.s..

For,

dlnx(t)=1x(λ−dx(t)−ex(t)y(t)−xσ12)dt+σ1dB1(t)≤[λx−(d+12σ12)]dt+σ1dB1(t). (23)

From (23), we can obtain

dlnx(t)≥−(d+12σ12)dt,

and

1dlnx(t)≤−1(d+12σ12)dt. (24)

Meanwhile,

λx≥dlnx(t)+(d+12σ12)+σ1dB1(t),

which indicates that

x≤λdlnx(t)+(d+12σ12)+σ1dB1(t)≤λd+12σ12+λdlnx(t)+σ1dB1(t). (25)

There exists a small number σ2, such that

∫0tx(s)ds≤λd+12σ12t+∫0tλdlnx(s)+σ1dB1(s)ds≤λd+12σ12t+λ∫0t1dlnx(s)ds≤λd+12σ12t−λ∫0t1(d+12σ12)ds≤λd+12σ12t≤λa(d+12σ12)(a+12σ22)t. (26)

Taking the superior limit and using the stochastic comparison theorem, combining (26), we obtain

lim supt→∞lny(t)t=lim supt→∞e1t∫0tx(s)ds−(a+12σ22)≤eλa(d+12σ12)(a+12σ22)−(a+12σ22)=(a+12σ22)(λea(a+12σ22)2(d+12σ12)−1)=(a+12σ22)(R0*−1)<0a.s.. (27)

Therefore, this indicates that

limt→∞y(t)=0a.s..

Consequently, this means that the virus will be eradicated in a long time. This completes the proof. □

6. Examples and Numerical Simulations

In this section, we will introduce some examples and numerical simulations to demonstrate the above theoretical results. Using the Milstein higher-order method developed in [23], we obtain the discretization equation of the system (3).

x(k+1)=x(k)+[λ−dx(k)−ex(k)y(k)]▵t+σ1x(k)▵tξk+σ12x(k)2▵t(ξk2−1),y(k+1)=y(k)+[ex(k)y(k)−ay(k)−py(k)z(k)]▵t+σ2y(k)▵tηk+σ22y(k)2▵t(ηk2−1),z(k+1)=z(k)+[cw(k)−bz(k)]▵t+σ3z(k)▵tζk+σ32z(k)2▵t(ζk2−1),w(k+1)=w(k)+σ[y(k)−w(k)]▵t. (28)

where the time increment ▵t is positive, and ξk,ηk,ζk are the Gaussian random variables which follow the distribution N(0,1),k=1,2,3.

In system (3), according to [27]:

Example 1.

In order to check the existence of an ergodic stationary distribution, we choose the values of the system parameters as follows: (σ1,σ2,σ3)=(0.1,0.1,0.1), λ=1000,d=0.1,e=0.002,a=5,p=0.2,c=0.2,b=0.3,σ=0.2, then R0*=3.208>1, where R0* is defined before Theorem 2 and choosing c1=−15,M=7. In other words, the conditions of Theorem 2 hold, and there is an ergodic stationary distribution μ(·) of system (3), which will persist for a long time. Figure 1 confirms this.

Figure 1.

Figure 1

The red curve represents the result of the stochastic model, whereas the green curve represents the result of the deterministic model. The right column shows the density function of the stochastic model (3). Choosing (σ1,σ2,σ3)=(0.1,0.1,0.1), when R0*=3.208>1, the disease will persist for a long time.

Example 2.

In order to check the extinction of the system (3), we choose the values of the system parameters as follows: (σ1,σ2,σ3)=(0.1,0.1,0.1), λ=250,d=0.1,e=0.002,a=5,p=0.2,c=0.2,b=0.3,σ=0.2; then, R0*=0.849<1, where R0* is defined before Theorem 3 and choosing c1=−20,M=5. In other words, the conditions of Theorem 3 hold, which will be extinct in a long time. Figure 2 confirms this.

Figure 2.

Figure 2

The red curve represents the result of the stochastic model, whereas the green curve represents the result of the deterministic model. The right column shows the density function of the stochastic model (3). Choosing (σ1,σ2,σ3)=(0.1,0.1,0.1), when R0*=0.849<1, the disease will be extinct in a long time.

7. Discussion

This paper considers the parameters d, a, and b disturbed by the white noise and assumes the dynamics of the corresponding stochastic system (3) with the time delay and CTL responsiveness. The reason for choosing the three disturbed parameters is that these three parameters are important in controlling the viral disease. Of course, in the following research, we will focus on the general situation to investigate the influence of white noise.

Acknowledgments

This work is supported by the National Natural Science Foundation of China (No.11871473) and Shandong Provincial Natural Science Foundation (No.ZR2019MA010).

Author Contributions

Conceptualization, J.S., M.G., and D.J.; methodology, J.S.; software, J.S.; validation, J.S., M.G., and D.J.; formal analysis, D.J.; resources, J.S.; data curation, M.G. and D.J.; writing—original draft preparation, J.S.; writing—review and editing, J.S., M.G., and D.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

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