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. 2021 Oct 26;2021(1):473. doi: 10.1186/s13662-021-03621-4

Mathematical analysis of a cancer model with time-delay in tumor-immune interaction and stimulation processes

Kaushik Dehingia 1, Hemanta Kumar Sarmah 1, Yamen Alharbi 2, Kamyar Hosseini 3,
PMCID: PMC8546790  PMID: 34721555

Abstract

In this study, we discuss a cancer model considering discrete time-delay in tumor-immune interaction and stimulation processes. This study aims to analyze and observe the dynamics of the model along with variation of vital parameters and the delay effect on anti-tumor immune responses. We obtain sufficient conditions for the existence of equilibrium points and their stability. Existence of Hopf bifurcation at co-axial equilibrium is investigated. The stability of bifurcating periodic solutions is discussed, and the time length for which the solutions preserve the stability is estimated. Furthermore, we have derived the conditions for the direction of bifurcating periodic solutions. Theoretically, it was observed that the system undergoes different states if we vary the system’s parameters. Some numerical simulations are presented to verify the obtained mathematical results.

Keywords: Tumor-immune model, Delay, Stability, Hopf bifurcation, Numerical simulations

Introduction

Cancer can be classified as abnormal growth and uncontrolled division of normal cells. The development of cancer is a complex phenomenon. The research community still does not understand the growth law of cancer and the immune system’s response in a tumor’s presence. However, research has proven that the immune system can eliminate tumor cells once they recognize those as malignant. So, in recent years, research on tumor-immune dynamics has gained more interest for the applied mathematicians, biologists, oncologists, and scientists. Mathematical modeling is an intelligent tool to gain insight into any real-world complex system. For example, COVID-19 disease has been creating havoc throughout the world during the last two years. Rezapour et al. [1] presented an SEIR epidemic model for the transmission of COVID-19 using the Caputo fractional derivative to find some remedial measures. Based on actual data and fitted in the model, the authors predicted the transmission of COVID-19 for the world in general and Iran in particular. In work [2], Rezapour and Mohammadi studied an AH1N1 influenza model by using the Caputo–Fabrizio fractional-order derivative. They calculated the model results for different fractional order and compared those with the results of the integer-order model. Aydogan et al. [3] examined a Caputo–Fabrizio fractional-order mathematical model of Rabies disease with the use of the Laplace Adomian decomposition method. A box model of mumps-induced hearing loss in children using the Caputo–Fabrizio fractional-order derivative that preserves the system’s historical memory was investigated in [4]. The authors also determined the optimal control problem for the proposed model considering treatment as a control parameter to reduce the infected population. By examining the sensitivity of basic reproduction numbers to each of the model parameters, they showed that the basic reproduction number increases with the increase of disease transmission rate and daily birth rate. Also, it reduces with an increase in the recovery rate, normal mortality rate.

The tool of mathematical modeling is widely used by researchers in the field of cancer modeling too. Several significant works [59] through mathematical modeling have been done to understand the response of the immune system with tumor. In [5], the authors analyzed a cancer model by considering the interactions between cancer cells, tumor angiogenesis and endothelial cells. Lopez et al. [6] estimated the decay rate of tumor cells in the presence of immune response and set a threshold value for which the immune system can eradicate the tumor. Dong et al. [7] explored the effect of CD4+T cells in a tumor-immune system incorporated with adoptive cellular immunotherapy (ACI) and suggested that CD4+T cells play a crucial role in the tumor eradication process under ACI therapy. Arlotti et al. [8] proposed a bilinear model of integro-differential equations to describe the dynamics of cellular interaction between tumor and immune cells. By introducing two phases, namely, the Inter-phase and M-phase at which cells are generally divided, Awang et al. [9] newly described the interactions between tumor cells and immune system. Zeng and Ma [10] analyzed a deterministic tumor-immune model under the Allee effect. This Allee effect disturbed the growth and reproduction of tumor-immune cells. They found a range of Allee threshold values for which the system can be stabilized.

The cytotoxic T cells are primarily responsible for tumor suppression and are found in all tissues in the body. Kuznetzov et al. [11] described the response of CTL cells to the growth of an immunogenic tumor. Quinonez et al. [12] examined a mathematical model to show the immune response in the presence of synthetic tumor vaccines to mitigate developing cancer. Li and Li [13] modified the Kuznetsov et al. [11] and Galach model [14] to a stochastic one by perturbing environmental noise. They found that the reduced rate of tumors in their model is faster than in the earlier models. Also, their result reveals that environmental noise is favorable for the extinction of tumor cells under immune surveillance, and noise is ineffective when the immune system’s ability is strong enough. De Pillis et al. [15] explored the role of natural killer (NK) and CD8+T cells in the immune-tumor interaction mechanism and tumor surveillance through a mathematical model. Another mathematical model was developed by Dritschel et al. [16] to investigate the anti-tumor immune response of helper and cytotoxic T cells. They concluded that the tumor growth could be reduced if we use treatments like IL-2 therapy, adoptive T cell therapy which boosts the immune system, and antibody therapy which blocks tumor-induced immuno-suppression. Recently, Pang et al. [17] proposed a modified model of [18, 19] to reflect the clinical phenomena of anti-tumor immune responses and observed that the tumor cells show initial exponential growth to the final stable position at zero depending upon the flow rate of mature immune cells.

In many biological complex systems, time delay plays a vital role. The introduction of time delay forces a system to depend not only on the present state but also on the past state. In cancer modeling, the time delay can describe the required time for cell differentiation, cell proliferation, the response of one cell to other cells, etc. Banerjee and Sarkar [20] studied a delay-induced tumor-immune model to control the growth of malignant cells. They varied parameters, analyzed the model, and observed that Hopf bifurcation occurs for delay term as the bifurcation parameter. Rihan et al. [21] considered a family of differential models to explore the effects of ACI therapy to control tumor burden. In a study of Bi and Xiao [22], they illustrated the bifurcation analysis of a modified version of the Kuznetsov model [11] with the introduction of two-time delays for immune response into the model. Khajanchi [23] and Khajanchi et al. [24] analyzed in detail the influence of time delay on the chaotic dynamics of tumor-immune interaction model [25]. In [23, 24], the authors presented that in the presence of delay, the model shows long-term chaotic behavior with Hopf bifurcations. They also estimated the length of the time delay to preserve stability and direction of Hopf bifurcation. Ghosh et al. [26] described the interaction between tumor cells and micro-environment immune and host cells with the use of two time delays, one for immune interaction with tumor and the other for immune action on the tumor. Dong et al. [27] converted their previously proposed model [7] to a delayed one with the use of two delays, namely the immune activation delay for ECs and immune activation delay for HTCs. Their results showed that the unstable equilibrium goes to a stable position for the activation delay of HTCs. In the work [28], the authors modified the model proposed by Dong et al. [7] with the use of one delay term for the activation of ECs by HTCs. This delay term induced two effects on the model. The first effect is that stability switches to instability, and the second stabilizes tumor-presence equilibrium. Further modification of the model [7] was carried out by Das et al. [29] with the use of distributed and discrete-time delay. They observed that uniform activation of helper T-cells can help in ECs stimulation and tumor control. Considering a reaction-diffusion system, including time delay under the Neumann boundary conditions, Kayan et al. [30] modified the model [11] which described tumor-immune competitions. They studied the Hopf bifurcation analysis and found that the effect of diffusion of tumor-immune interaction can significantly change the dynamics of the model.

In this article, we investigate the model proposed by Pang et al. [17] introducing delay term for anti-tumor immune responses of matured T lymphocytes to destroy tumor cells. In Sect. 2, we formulate our proposed model. A qualitative analysis is done in Sect. 3. In Sect. 4, conditions of Hopf bifurcation of the system are analyzed. Section 5 and Sect. 6 deal with the stability of the limit cycle and direction and stability of Hopf bifurcation. Numerical examples, discussion, and conclusions are carried out in respective Sects. 7 and 8.

The model

Mathematical models can give a better insight into tumor-immune interaction. In the above literature, we have found that each model is proposed to understand the tumor cells’ mechanism and reduce the tumor burden in the body. T lymphocytes are the most important cells in the immune system, capable of killing the tumor cells through kinetic processes. However, it is important to note that the tumor cells can also compete with T lymphocytes and make them functionally inactive. Also, tumor cells secrete cytokines, which are responsible for tumor cells proliferation. As a result, eradicating all tumor cells becomes difficult for T lymphocytes, and a time delay occurs for the deactivation of tumor cells by T lymphocytes. This time delay is regarded as an interaction and stimulation delay of the tumor-immune system. We account for this time delay, the model of Pang et al.[17] is thus modified into a delay system as follows:

dL1(τ)dτ=μλ1L1(τ)+α1T(τΔ)L2(τΔ)η+T(τΔ),dL2(τ))dτ=λ1L1(τ)α3L2(τ),dT(τ)dτ=λ2T(τ)α2T(τΔ)L2(τΔ),} 2.1

where L1(τ), L2(τ), and T(τ) are densities of immature T lymphocytes, mature T lymphocytes, and tumor cells at any time τ respectively.

In the first equation of (2.1), the first term μ describes the fixed production rate of immature T lymphocytes by the body in the absence of tumor cells. The second term λ1L1(τ) is used for describing the transformation rate of immature T lymphocytes to mature T lymphocytes. The third term α1T(τΔ)L2(τΔ)η+T(τΔ) describes the recruitment term of anti-tumor immune response, where α1 is the maximum recruitment rate and η is the half-saturation constant. Here, Δ represents the discrete-time delay factor added for interaction and stimulation delay of the tumor-immune system. The second equation describes the dynamics of mature T lymphocytes where α3 is the inactivation rate of T lymphocytes. The third equation designates the rate of change of tumor cells in which tumor cells can grow exponentially in the absence of immune response, where λ2 is the exponential tumor growth rate. The term α2T(τΔ)L2(τΔ) describes the interaction between tumor and mature T lymphocytes, where α2 is the rate of tumor cells killed by the mature T lymphocytes.

For the sake of discussion of model (2.1), we substitute μ=λ0L0 and use nondimensional variables and parameters as

(x,y,z)=(α2α1(L1λ0λ1L0),α2λ1L2,Tη)with t=λ1τ,

and

(a1,a2,a3,a4)=(α1λ1,α3λ1,α2λ0λ12L0,λ2λ1).

The normalized model of (2.1) is

dxdt=x+y(tΔ)z(tΔ)1+z(tΔ),dydt=a1xa2y+a3,dzdt=a4zy(tΔ)z(tΔ),} 2.2

with initial history:

x(θ)=ϕ1(θ),y(θ)=ϕ2(θ),z(θ)=ϕ3(θ), 2.3

with ϕi0, i=1,2,3 for θ[Δ,0], where ϕi(θ)R+3 are the continuous functions on [Δ,0) that may display jumps at θ=0.

Qualitative analysis

Basic properties

The following proposition establishes the nonnegativity of the solutions of (2.2) with (2.3).

Theorem 3.1

The solution (x(t),y(t),z(t)) of system (2.2) is nonnegative under the nonnegative initial conditions (ϕ(i), i=1,2,3) defined on [0,+).

Proof

System (2.2) can be written as

X˙=(x˙(t)y˙(t)z˙(t))=(x+y(tΔ)z(tΔ)1+z(tΔ)a1xa2y+a3a4zy(tΔ)z(tΔ))=(V1(X)V2(X)V3(X))=V(X), 3.1

where the function V:R+3R3 for VC(R+3) is defined in the nonnegative octant R+3. The R.H.S. of system (3.1) is locally Lipschitz, and hence the derivatives are bounded, satisfy the conditions

Vi(X)|Xi(t),XR+3=Vi(0)0i=1,2,3. 3.2

According to the lemma by Yang et al. [31], every solution of system (2.2) with initial values (2.3), ϕi(t)R+3, say, X(t)=X[t;X(0)], t>0, that is, it remains positive throughout the region R+3, t>0. □

System (2.2) without time delay was discussed in [17]. Since inducing time delay does not affect the existence conditions for equilibria of the system, the system has three equilibria with E0(0,0,0) as a trivial equilibrium, E1(0,a3a2,0) as a tumor-free one, which always exist, and E2(a2a4a3a1,a4,a2a4a3a3+a1a4a2a4) as a co-axial equilibrium, which exists for max{0,(a2a1a4)}<a3<a2a4.

  • For a3>a2a4, the tumor-free equilibrium E1(0,a3a2,0) exists.

  • There exists only one equilibrium E1 for a2>a1 and 0<a3<(a2a1)a4.

  • For a2<a1 and 0<a3<a2a4, two equilibria E1 and E2 exist.

  • For a2>a1 and (a2a1)a4<a3<a2a4, two equilibria E1 and E2 exist.

Local stability

In order to check the local stability at each of the equilibrium points, we calculate the following Jacobian matrix for the system (2.2):

JE=(1z1+zeλΔy(1+z)2eλΔa1a200zeλΔa4yeλΔ). 3.3
  • I.

    The “no living cell” fixed point E0(0,0,0) is stable if a4<0. As corresponding to E0, the eigenvalues of the matrix (3.3) are λ0,1=1 (<0), λ0,2=a2 (<0), and λ0,3=a4.

  • II.

    The eigenvalues of the matrix (3.3) are λ1,1=1, λ1,2=a2, and λ1,3=a3a2a4a2 corresponding to the tumor-free fixed point E1(0,a3a2,0). So, E1 is stable if a3>a2a4, otherwise unstable. For the case of a2>a1 and 0<a3<(a2a1)a4, the fixed point E1 is a saddle-focus point with two negative eigenvalues and one positive eigenvalue.

  • III.
    Now, we will investigate the dynamical behavior of the system (2.2) around the co-axial fixed point E2(xˆ=a2a4a3a1,yˆ=a4,zˆ=a2a4a3a3+a1a4a2a4) under the influence of discrete time lag Δ for both the cases of existence of E2. In this case, the eigenvalues of matrix (3.3) can be found from the following equation:
    λ3+(1+a2a4+yˆeλΔ)λ2+{a2a4a2a4+(a2yˆ+yˆa1zˆ1+zˆ)eλΔ}λ+{a2a4+(a1a4zˆ1+zˆ+a2yˆ)eλΔ}=0. 3.4
    For the case of no time lag (Δ=0), equation (3.4) becomes
    λ3+(1+a2a4+yˆ)λ2+(a2a4a2a4+a2yˆ+yˆa1zˆ1+zˆ)λ+(a2a4+a1a4zˆ1+zˆ+a2yˆ)=0. 3.5
    By the use of Routh–Hurwitz criterion to (3.5), E2 is asymptotically stable if the following conditions are satisfied:
    1+a2a4+yˆ>01+a2>0,(a2a4+a1a4zˆ1+zˆ+a2yˆ)>0a1a4>0,(1+a2a4+yˆ)(a2a4a2a4+a2yˆ+yˆa1zˆ1+zˆ)a1a4zˆ1+zˆ>0(1+a2)(a2a1zˆ1+zˆ)a1a4zˆ1+zˆ>0(1+a2)(a2a1zˆ1+zˆ)>a1a4zˆ1+zˆ.} 3.6
    Now, we shall analyze the dynamical behavior of the system (2.2) with time lag Δ0. For this, we assume that there exists a purely imaginary root for (3.4). Hence, we substitute λ=im(m>0) into (3.4) and, separating the real and imaginary parts, we have
    (1+a2a4)m2(a2a4)=(a1a4zˆ1+zˆ+a2yˆyˆm2)cos(mΔ)(1+a2a4)m2(a2a4)=+(a2yˆ+yˆa1zˆ1+zˆ)msin(mΔ),andm3(a2a2a4a4)m=(a2yˆ+yˆa1zˆ1+zˆ)mcos(mΔ)m3(a2a2a4a4)m=(a1a4zˆ1+zˆ+a2yˆyˆm2)sin(mΔ).} 3.7
    Using the method of cross-multiplication, we solve both the equations of (3.7) and get
    tan(mΔ)=cde+f, 3.8
    where
    c=(a2yˆ+yˆa1zˆ1+zˆ)m{(1+a2a4)m2(a2a4)},d={m3(a2a2a4a4)m}{a1a4zˆ1+zˆ+a2yˆyˆm2},e={(1+a2a4)m2(a2a4)}{a1a4zˆ1+zˆ+a2yˆyˆm2},f=(a2yˆ+yˆa1zˆ1+zˆ)m{m3(a2a2a4a4)m}.
    By squaring and adding both sides of both the equations of (3.7), we get
    m6+p0m4+p1m2+p2=0, 3.9
    where
    p0=(1+a2a4)22(a2a2a4a4)yˆ2,p1=(a2a2a4a4)22(1+a2a4)(a2a4)p1=+2yˆ(a1a4zˆ1+zˆ+a2yˆ)(a2yˆ+yˆa1zˆ1+zˆ)2,p2=a22a42{a1a4zˆ1+zˆ+a2yˆ}2.} 3.10
    The equation (3.9) will have a positive root if
    p0=(1+a2a4)22(a2a2a4a4)yˆ2>0,
    and
    p2=a22a42{a1a4zˆ1+zˆ+a2yˆ}2<0.
    Suppose that m0 is a unique non-negative root of the equation (3.9) such that (3.4) has a pair of purely imaginary roots of the form ±im0. Then from the equation (3.8) the time lag Δk corresponding to m0 is
    Δk=1m0arctan[c0d0e0+f0]+2kπm0,k=0,1,2,3,, 3.11
    where
    c0=(a2yˆ+yˆa1zˆ1+zˆ)m0{(1+a2a4)m02(a2a4)},d0={m03(a2a2a4a4)m0}{a1a4zˆ1+zˆ+a2yˆyˆm02},e0={(1+a2a4)m02(a2a4)}{a1a4zˆ1+zˆ+a2yˆyˆm02},f0=(a2yˆ+yˆa1zˆ1+zˆ)m0{m03(a2a2a4a4)m0}.
    Therefore, the co-axial equilibrium E2 is locally asymptotically stable under the conditions (3.6) for Δk=0. So, this point will also remain stable for Δk<Δ0, where Δk=Δ at k=0 by Butler’s lemma [24]. This suggest that for Δk>Δ0 the co-axial equilibrium E2 is unstable. This implies that the tumor cells can proliferate faster if the interaction time delay crosses a given critical value and the system loses its stability at E2.

The rest of the work which is discussed in Sect. 4, Sect. 5, and Sect. 6 is inspired and followed by the previous works [20, 23, 24, 32, 33].

Analysis of Hopf bifurcation

As the equation (3.4) has a complex roots of the form λ=im0, it implies that the system (2.2) may undergo a Hopf bifurcation at Δ=Δk and around the equilibrium E2. Here, we establish a condition for which the system (2.2) undergoes a Hopf bifurcation by using Lemma 1 [17]. For this, first we need to verify the transversality condition d(Reλ)dΔ|Δ=Δk>0.

Differentiating (3.4) with respect to Δ gives

[{3λ2+2λ(1+a2a4)+(a2a2a4a2)}+eλΔk{2λyˆ+a2yˆ+yˆa1zˆ1+zˆ}ΔeλΔk{yˆλ2+(a2yˆ+yˆa1zˆ1+zˆ)λ+a1a4zˆ1+zˆ+a2yˆ}]dλdΔk=λeλΔk{yˆλ2+(a2yˆ+yˆa1zˆ1+zˆ)λ+a1a4zˆ1+zˆ+a2yˆ}. 4.1

Simplifying equation (4.1), we have

(dλdΔk)1=2λ3+(1+a2a4)λ2+a2a4λ2{λ3+(1+a2a4)λ2+(a2a2a4a4)λa2a4}+yˆλ2(a1a4zˆ1+zˆ+a2yˆ)λ2{yˆλ2+(a2yˆ+yˆa1zˆ1+zˆ)λ+a1a4zˆ1+zˆ+a2yˆ}Δkλ. 4.2

Therefore, with the increase of the value of Δk the direction of motion of λ is given by

Π=sign{Re(dλdΔk)1}λ=im0=sign[Re(2λ3+(1+a2a4)λ2+a2a4λ2{λ3+(1+a2a4)λ2+(a2a2a4a4)λa2a4}+yˆλ2(a1a4zˆ1+zˆ+a2yˆ)λ2{yˆλ2+(a2yˆ+yˆa1zˆ1+zˆ)λ+a1a4zˆ1+zˆ+a2yˆ}Δkλ)]λ=im0,Π=1m02Π=×sign[2m06+m04{(1+a2a4)22(a2a2a4a2)yˆ2}+{(a1a4zˆ1+zˆ+a2yˆ)2a22a42}(a2yˆ+yˆa1zˆ1+zˆ)2m02+(a1a4zˆ1+zˆ+a2yˆyˆm02)2]. 4.3

For d(Reλ)dΔ|Δ=Δk>0, from the equation (4.3) we must have

{(1+a2a4)22(a2a2a4a2)yˆ2}>0,and{(a1a4zˆ1+zˆ+a2yˆ)2a22a42}>0.} 4.4

Theorem 4.1

The co-axial equilibrium E2 is

  • (i)

    asymptotically stable if Δ ∈ [0,Δk),

  • (ii)

    unstable if Δ>Δk,

  • (iii)

    Hopf bifurcation occurs around E2 if Δ=Δk.

Stability of limit cycle: length of time lag estimation

In this section, we investigate the stability of bifurcating periodic solutions and estimate the length of time lag preserving the stability of period-1 limit cycle. Consider model (2.2) and the space of all continuous real-valued functions defined on [Δ,+), which satisfies the initial history (2.3) on the interval [Δ,0). First, we linearize model (2.2) around the co-axial equilibrium point E2(xˆ=a2a4a3a1,yˆ=a4,zˆ=a2a4a3a3+a1a4a2a4), which gives us

x˙=x+zˆ1+zˆy(tΔ)+yˆ(1+zˆ)2z(tΔ),y˙=a1xa2y,z˙=zˆy(tΔ)+a4zyˆz(tΔ).} 5.1

Using Laplace transformation into (5.1), we have

(ω+1)Lx(ω)=zˆ1+zˆeωΔLy(ω)+zˆ1+zˆeωΔUy(ω)(ω+1)Lx(ω)=+yˆ1+zˆeωΔLz(ω)+yˆ1+zˆeωΔUz(ω)+x¯(0),(ω+a2)Ly(ω)=a1Lx(ω)+y¯(0),(ωa4+yˆeωΔ)Lz(ω)=zˆeωΔLy(ω)zˆeωΔUy(ω)(ωa4+yˆeωΔ)Lz(ω)=yˆeωΔKz(ω)+z¯(0),} 5.2

where Uy(ω)=Δ0eωΔy(t)dt, Uz(ω)=Δ0eωΔz(t)dt and Lx(ω), Ly(ω), and Lz(ω) are the Laplace transformations of x(t), y(t), and z(t) respectively.

Now, by using the theory provided by Freedman et al. [34] and the classical Nyquist criteria, the equilibrium point E2 is asymptotically stable if, for the equation

P(ω)=ω3+(1+a2a4+yˆeωΔ)ω2+{a2a4a2a4+(a2yˆ+yˆa1zˆ1+zˆ)eωΔ}ω+{a2a4+(a1a4zˆ1+zˆ+a2yˆ)eωΔ}, 5.3

the following conditions hold:

ReP(iζ0)=0, 5.4
ImP(iζ0)=0, 5.5

where ζ0 is the minimal nonnegative root of (5.4) and (5.5).

From (5.4),

(1+a2a4)ζ02=a2a4+(a1a4zˆ1+zˆ+a2yˆ)cos(ζ0Δ)yˆζ02cos(ζ0Δ)+(a2yˆ+yˆa1zˆ1+zˆ)ζ0sin(ζ0Δ). 5.6

Using the inequalities |cos(ζ0Δ)|1 and |sin(ζ0Δ)|1, we get

|(1+a2a4)|ζ02|a2a4|+|(a1a4zˆ1+zˆ+a2yˆ)|+|yˆ|ζ02+|(a2yˆ+yˆa1zˆ1+zˆ)|ζ0. 5.7

From (5.7) we have

ζ+|(a2yˆ+yˆa1zˆ1+zˆ)|+(a2yˆ+yˆa1zˆ1+zˆ)2+4{|(1+a2a4)||yˆ|}{|a2a4|+|(a1a4zˆ1+zˆ+a2yˆ)|}2{|(1+a2a4)||yˆ|}. 5.8

Hence, ζ0ζ+.

From equation (5.5)

ζ02<(a2a2a4a4)+(a2yˆ+yˆa1zˆ1+zˆ)cos(ζ0Δ)(a1a4zˆ1+zˆ+a2yˆ)sin(ζ0Δ)ζ0+yˆζ0sin(ζ0Δ).} 5.9

Using (5.6), equation (5.9) becomes

{(a1a4zˆ1+zˆ+a2yˆ)yˆζ02(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)}[cos(ζ0Δ)1]+[{a2yˆ+yˆa1zˆ1+zˆ(1+a2a4)yˆ}ζ0+(1+a2a4)(a1a4zˆ1+zˆ+a2yˆ)ζ0]sin(ζ0Δ)<(1+a2a4)(a2a2a4a4)(a2a4)+(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)(a1a4zˆ1+zˆ+a2yˆ)+yˆζ02.} 5.10

Using the inequality ζ02<(a2a2a4a4+a2yˆ+yˆa1zˆ1+zˆ) for Δ=0, the above equation has the form

{(a1a4zˆ1+zˆ+a2yˆ)yˆζ02(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)}[cos(ζ0Δ)1]+[{a2yˆ+yˆa1zˆ1+zˆ(1+a2a4)yˆ}ζ0+(1+a2a4)(a1a4zˆ1+zˆ+a2yˆ)ζ0]sin(ζ0Δ)<(1+a2a4+yˆ)(a2a2a4a4+a2yˆ+yˆa1zˆ1+zˆ){a2a4+a1a4zˆ1+zˆ+a2yˆ}.} 5.11

Now the first term and the second term of the L.H.S. of (5.11) can be written respectively as

{(a1a4zˆ1+zˆ+a2yˆ)yˆζ02(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)}[cos(ζ0Δ)1]=2[yˆζ02+(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)(a1a4zˆ1+zˆ+a2yˆ)]sin2(ζ0Δ2)12ζ+2|{yˆζ02+(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)(a1a4zˆ1+zˆ+a2yˆ)}|Δ2,}

and

[{a2yˆ+yˆa1zˆ1+zˆ(1+a2a4)yˆ}ζ0+(1+a2a4)(a1a4zˆ1+zˆ+a2yˆ)ζ0]sin(ζ0Δ)[|{a2yˆ+yˆa1zˆ1+zˆ(1+a2a4)yˆ}|ζ+2+|(1+a2a4)||(a1a4zˆ1+zˆ+a2yˆ)|]ΔM.}

Therefore from (5.11)

χ1Δ2+χ2Δχ3, 5.12

where

χ1=12ζ+2|{yˆζ02+(1+a2a4)(a2yˆ+yˆa1zˆ1+zˆ)(a1a4zˆ1+zˆ+a2yˆ)}|,χ2=[|{a2yˆ+yˆa1zˆ1+zˆ(1+a2a4)yˆ}|ζ+2+|(1+a2a4)||(a1a4zˆ1+zˆ+a2yˆ)|],χ3=(1+a2a4+yˆ)(a2a2a4a4+a2yˆ+yˆa1zˆ1+zˆ){a2a4+a1a4zˆ1+zˆ+a2yˆ}.}

Now, equation (5.12) gives

Δ+=12χ1[χ2+χ22+4χ1χ3]for 0ΔΔ+. 5.13

Therefore, the system (2.2) preserves the stability around the equilibrium E2 for the maximum length of the time lag Δ+ with period-1 limit cycle.

Direction and stability of Hopf bifurcation

In the previous sections, we have discussed the conditions for which the periodic solutions of the system (2.2) bifurcate from co-axial equilibrium E2 at the critical values of Δk via the Hopf bifurcation. In this section, we will analyze the direction, stability, and periods of the periodic solutions of the system (2.2) using normal theory and the center manifold theorem developed by Hassard et al. [35].

Let u1(t)=x(t)x¯, u2(t)=y(t)y¯, u3(t)=z(t)z¯, x(t)=u1(Δt), y(t)=u2(Δt), z(t)=u3(Δt), and Δ=Δ0+μ, where Δ0 is defined by (3.11), and μR. The system (2.2) can be written as a functional differential equation in C=C([1,0],R3) as

X=Lμ(Xt)+f(μ,Xt), 6.1

where X(t)=(x(t),y(t),z(t))TR3, and Lμ:CR3, f:R×CR3 are given, respectively, as follows: for Φ(t)=(Φ1(t),Φ2(t),Φ3(t))TC([Δ,0],R3), we define

Lμ(Φ)=D1Φ(0)+D2Φ(1), 6.2

and

f(μ,Φ)=(Δ0+μ)M, 6.3

where

D1=(Δ0+μ)(100a1a2000a4),D2=(Δ0+μ)(0z¯1+z¯y¯(1+z¯)20000z¯y¯), 6.4
M=(Φ2(1)Φ3(1)Φ2(1)Φ32(1)+HOT0Φ2(1)Φ3(1)), 6.5

HOT → higher order terms.

By the Riesz representation theorem, there exists a matrix function η(θ,μ) of bounded variation for θ[1,0] such that

Lμ(Φ)=10dη(θ,μ)Φ(θ)for ΦC. 6.6

For the Dirac delta function δ, choose

η(θ,μ)=D1δ(θ)+D2δ(θ+1), 6.7

and for ΦC1([1,0],R3), define

A(μ)Φ(θ)={dΦ(θ)dθ,θ[1,0),10dη(s,μ)Φ(s),θ=0, 6.8

and

R(μ)Φ(θ)={0,θ[1,0),f(μ,θ),θ=0. 6.9

Hence, system (6.1) is equivalent to the operator equation

X=A(μ)Xt+R(μ)Xt, 6.10

where Xt(θ)=X(t+θ) for θ[1,0).

For ΨC1([1,0),(R3)), define

AΨ(s)={dΨ(s)ds,s(0,1],10dηT(t,0)Ψ(t),s=0, 6.11

and the bilinear inner product

Ψ(s),Φ(θ)=Ψ¯(0)Φ(0)θ=10ξ=0θΨ¯(ξθ)dη(θ)Φ(ξ)dξ, 6.12

where η(θ)=η(θ,0). Then A(0) and A are adjoint operators. We already assume that ±ιω0Δk are the eigenvalues of A(0). Hence, the eigenvalues of A are ιω0Δk. We need to compute the eigenvectors of A(0) and A corresponding to the eigenvalues ιω0Δk and ιω0Δk respectively.

Suppose that v(θ)=(1,v1,v2)Teιω0Δkθ is the eigenvector of A(0) corresponding to ιω0Δk. Then A(0)v(0)=ιω0Δkv(0). It follows from the definition of A(0) and (6.3), (6.6) and (6.7) that

Δk(100a1a2000a4)v(0)+Δk(0z¯1+z¯y¯(1+z¯)20000z¯y¯)v(1)=ιω0Δkv(0).

Then, for v(1)=v(0)eιω0Δk, we obtain

v1=a1a2+ιω0;v2=a1z¯eιω0Δk(a2+ιω0)(ιω0+y¯eιω0Δk).

In a similar manner, we can obtain the eigenvector v(s)=D(1,v1,v2)Teιω0Δks of A corresponding to ιω0Δk, where

v1=1ιω0a1;v2=y¯(1+y¯)2(ιω0y¯eιω0Δk)eιω0Δk.

In order to guarantee v(s),v(θ)=1, we need to determine the expression of D

v(s),v(θ)=D¯(1,v1¯,v2¯)(1,v1,v2)Tθ=10ξ=0θD¯(1,v1¯,v2¯)eιω0Δk(ξθ)dη(θ)(1,v1,v2)Teιω0Δkξdξ=D¯{(1+v1¯v1+v2¯v2)θ=10(1,v1¯,v2¯)θeιω0Δkθdη(θ)(1,v1,v2)T}=D¯{(1+v1¯v1+v2¯v2)+{z¯1+z¯v1+y¯(1+z¯)2v2z¯v2¯v1y¯v2¯v2}Δkeιω0Δk}.

Therefore we can choose D as

D¯=[1(1+v1¯v1+v2¯v2)+{z¯1+z¯v1+y¯(1+z¯)2v2z¯v2¯v1y¯v2¯v2}Δkeιω0Δk].

On the other hand, due to adjoint property, we can write Ψ,AΦ=AΨ,Φ.

We have

ιω0Δkv,v¯=v,Av¯=Av,v¯=ιω0Δkv,v¯=ιω0Δkv,v¯.

Therefore, v,v¯=0.

Now, we will compute the coordinates describing the center manifold C0 at μ=0. Let Xt be the solution of (6.10) when μ=0. We define

Z(t)=v,Xt,W(t,θ)=Xtz(t)v(θ)z¯(t)v¯(θ)=Xt(θ)2Re{z(t)v(θ)}. 6.13

On the center manifold C0 we have W(t,θ)=W(z(t),z¯(t),θ), where

W(z,z¯,θ)=W20(θ)z22+W11(θ)zz¯+W02(θ)z¯22+W30(θ)z36+, 6.14

where z and are the local coordinates for the center manifold C0 in the direction of v¯ and v. Note that W is real if xt is real. Here, we are only interested in real solutions. From (6.13), we have

v,W=v,Xtzvz¯v¯=v,Xtzv,vzv,v¯=zz=0.

For the solution xtC0 in (6.10), since μ=0, hence

z˙(t)=v,X˙t=v,A(0)Xt+R(0)Xt=A(0)v,Xt+v¯(0)f(0,Xt)=ιω0Δkv,Xt+v¯(0)f0(z,z¯)=ιω0Δkz+v¯(0)f0(z,z¯)=ιω0Δkz(t)+g(z,z¯),

where

g(z,z¯)=v¯(0)f0(z,z¯)=g20z22+g11zz¯+g02z¯22+g21z2z¯2+. 6.15

From (6.13) and (6.14), it follows that

Xt=W(z,z¯,θ)+zv+z¯v¯.

Thus,

Xt=[X1t(θ)X2t(θ)X3t(θ)]=[W(1)(z,z¯,θ)W(2)(z,z¯,θ)W(3)(z,z¯,θ)]+z[1v1v2]eιω0Δkθ+z¯[1v¯1v¯2]eιω0Δkθ,

where

X1t(θ)=zeιω0Δkθ+z¯eιω0Δkθ+W201(θ)z22+W111(θ)zz¯+W021(θ)z¯22+,X2t(θ)=v1zeιω0Δkθ+v1¯z¯eιω0Δkθ+W202(θ)z22+W112(θ)zz¯+W022(θ)z¯22+,X3t(θ)=v2zeιω0Δkθ+v2¯z¯eιω0Δkθ+W203(θ)z22+W113(θ)zz¯+W023(θ)z¯22+.}

Using these values and from (6.3) it follows that

g(z,z¯)=v¯(0)f0(z,z¯)=v¯(0)f0(z,Xt)=ΔkD¯[1,v1¯,v2¯][X2t(1)X3t(1)X2t(1)X3t2(1)0X2t(1)X3t(1)]=ΔkD¯[X2t(1)X3t(1)X2t(1)X3t2(1)X2t(1)X3t(1)v2¯].} 6.16

Putting the values of X2t(1), X3t(1), and X3t2(1), computing the above expressions (6.16), and comparing the coefficients of z2, zz̄, z¯2, and z2z¯ with (6.15), we have

g20=2ΔkD¯(v1v2e2ιω0Δkv1v2v¯2e2ιω0Δk),g11=ΔkD¯(v1v¯2+v¯1v2v1v¯2v¯2v¯1v2v¯2),g02=2ΔkD¯(v¯1v¯2e2ιω0Δkv¯1v¯2v¯2e2ιω0Δk),g21=2ΔkD¯[v1eιω0ΔkW113(1)+v¯22eιω0ΔkW202(1)+v2eιω0ΔkW112(1)g21=+v¯12eιω0ΔkW203(1)2v1|v2|2eιω0Δkv¯1v22eιω0Δkg21=v¯2{v1eιω0ΔkW113(1)+v¯22eιω0ΔkW202(1)+v2eιω0ΔkW112(1)g21=+v¯12eιω0ΔkW203(1)}],} 6.17

and

W20(θ)=ιg20ω0Δkq(0)eιω0Δkθ+ιg¯023ω0Δkq¯(0)eιω0Δkθ+E1e2ιω0Δkθ,W11(θ)=ιg11ω0Δkq(0)eιω0Δkθ+ιg¯11ω0Δkq¯(0)eιω0Δkθ+E2,} 6.18

where E1=(E1(1),E1(2),E1(3)) and E2=(E2(1),E2(2),E2(3)) are a constant vector in R3 satisfying the following equations:

(1ιω0z¯1+z¯eιω0Δky¯(1+z¯)2eιω0Δka1a2ιω000z¯eιω0Δka4ιω0y¯eιω0Δk)(E1(1)E1(2)E1(3))=2(Γ11Γ21Γ31), 6.19
(1z¯1+z¯y¯(1+z¯)2a1a200z¯a4y¯)(E2(1)E2(2)E2(3))=2(Γ12Γ22Γ32), 6.20
Γ11=v1v2e2ιω0Δk,Γ12=v1v¯2+v¯1v2,Γ21=0,Γ22=0,Γ31=v1v2e2ιω0Δk,Γ32=v1v¯2v¯1v2.} 6.21

Furthermore, we can compute g21 with respect to parameters and delay. Hence, from the above analysis we can conclude that in order to find each gij we have to use the parameters and delay in system (2.2). Thus we can compute the following values:

c1(0)=ι2Δkω0(g11g202|g11|2|g02|23)+g212,μ2=Re{c1(0)}Re{λ(Δk)},β2=2Re{c1(0)},T2=Im{c1(0)}+μ2Imλ(Δk)Δkω0.} 6.22

Based on our analysis, by the result of Hassard et al. [35], we have the following result.

Theorem 6.1

The sign of μ2, β2, and T2 determines the directions of Hopf bifurcations, stability of the bifurcating periodic solutions, and the period of bifurcating periodic solutions respectively for Δ=Δk. In view of (6.22), the following results hold for system (2.2):

  1. If μ2<0 (μ2>0), the Hopf bifurcation is subcritical (supercritical).

  2. If β2>0 (β2<0), the bifurcation periodic solutions are unstable (stable).

  3. If T2<0 (T2>0), the period of the bifurcated periodic solution decreases (increases).

Numerical simulations

Through our above analysis, we have gained an analytical understanding of the possible dynamics of our proposed nonlinear delay differential equation model (2.2). In this section, bifurcation analysis and parameter sensitivity will be discussed. The delay model (2.2) showed that the system exhibited oscillations. Here, we shall discuss the effects of varying the parameter a1 on generating the oscillatory behavior. In Fig. 1, X is written as a function of a1. The curves (equilibrium branch) having red and black colors represent the stable and unstable steady state branches, respectively. Further, the green curve denotes the maximum and minimum of the limit cycle. The equilibrium branch loses its stability due to the appearance of a Hopf bifurcation point. In the unstable branch, the system (2.2) exhibits oscillations, and from the figure, it can be observed that the amplitude of these oscillations decreases as a1 increases.

Figure 1.

Figure 1

A bifurcation diagram showing X as a function of a1. Parameter values are a1=0.3, a2=0.6, a3=4, a4=10, and Δ=0.05

Similar effects of a2 on the steady states of X are discussed in Fig. 2. The red, black curves represent the stable and unstable steady state branches, whereas the green circle denotes the stable limit cycles. For low and high values of a2, the system (2.2) has a stable equilibrium point. The system (2.2), however, does not converge to a steady-state when a1=0 or a2=0. These are shown by arrows in Figs. 1 and 2. The reason for this is because the equilibrium expression E1 is divided by a2 and E2 is divided by a1. Hence, E1,E2.

Figure 2.

Figure 2

A bifurcation diagram showing X as a function of a2. Parameter values are a1=0.3, a2=0.6, a3=4, a4=10, and Δ=0.05

After discussing the effects of a1 and a2 on generating limit cycle oscillations, we need to investigate how the interplay between the two parameters a1 and a2 can alter these oscillations. To address this question, we shall track the two parameters on a two-parameter plot.

Figure 3 shows a two-parameter plot. Within the cusp, the system (2.2) exhibits oscillations. Outside the cusp, the model (2.2) only has a single stable steady-state. In the absence of a1 or a2, the system cannot generate limit cycle oscillations. For the model (2.2) to generate an oscillatory response, it must have a “well” balance between a1 and a2. If this balance is biased, the oscillatory response cannot be achieved.

Figure 3.

Figure 3

A two-parameter plot a1 vs a2 showing the effects of these two parameters on the oscillations. Parameter values are similar to Fig. 1

When selecting values of a1 and a2 from the region of oscillations of the figure, the model (2.2) shows oscillation. We shall focus on the effects of a3 on these oscillations. In other words, how does it alter this response? Figure 4 shows a two-parameter bifurcation diagram, and it shows that if either of these two parameters increases beyond a critical level, the oscillations will be destroyed. Additionally, in the absence of a3, the model (2.2) can generate an oscillatory behavior.

Figure 4.

Figure 4

A two-parameter plot a2 vs a3 showing the effects of these two parameters on the oscillations. Parameter values are similar to Fig. 1

Here, we shall focus numerically on the effects of the delay term on the limit cycle oscillations. Figure 5 illustrates the relationship between a1 and Δ on generating limit cycle oscillations. In this Figure, in the absence of the delay term, the system (2.2) can generate oscillations if a1 is increased beyond the blue vertical line (the Hopf locus).

Figure 5.

Figure 5

The interplay between a1 and Δ in order to generate oscillations. Parameter values are similar to Fig. 1

We shall consider the role of a2 and the delay term on generating oscillations and this can observe in Fig. 6. The system (2.2) can generate an oscillatory behavior even without the delay term as shown in Pang et al. model [17]. Figure 5 and Fig. 6 suggests that the system (2.2) requires greater a2 value than a1 value in order to be able to generate oscillations.

Figure 6.

Figure 6

A two-parameter plot showing the role of a2 and Δ on generating limit cycle oscillations. Parameter values are similar to Fig. 1

Figure 7 highlights the contribution of the parameters a3 and Δ on destabilizing the stable steady state branch. For the model (2.2) to generate oscillations, it requires greater a3 values than a1 and a2. Thus, the system (2.2) can cross the Hopf locus and generate an oscillatory behavior.

Figure 7.

Figure 7

A two-parameter plot showing the role of a3 and Δ on generating limit cycle oscillations. Parameter values are similar to Fig. 1

Figure 8 shows that the model (2.2) requires greater a4 values in order to exhibit oscillations that a1, a2, and a3.

Figure 8.

Figure 8

A two-parameter plot showing the role of a4 and Δ on generating limit cycle oscillations. Parameter values are similar to those in Fig. 1

However, suitable parameter values often give a meaningful biological scenario of the system (2.2). Therefore, we perform some simulation works for a better understanding of our analytical treatment. We consider different values of the parameters and the delay factor (Δ) to observe biologically plausible different dynamical scenarios of the model (2.2), enough to merit the mathematical study.

Choosing a1=0.3, a2=0.6, a3=4.0, a4=10.0, then a2>a1 and (a2a1)a4<a3<a2a4, which implies the existence of equilibria E1 and E2. Using the conditions of local stability, we get that both the equilibria E1 and E2 are unstable. Also, there occurs a periodic solution at E2. Figures 9 and 10 show the oscillating behavior as well as the periodic solutions for the system (2.2). Existence of periodic solutions is relevant in cancer models. It implies that the tumor levels may oscillate around a fixed point even in absence of any treatment. Such a phenomenon, which is known as Jeff’s phenomenon, has been observed clinically. We observe that Δ is beneficial for tumor cells. We observe no stability switch in the system (2.2) as the delay factor Δ increases.

Figure 9.

Figure 9

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=4.0, a4=10.0, Δ=0.01

Figure 10.

Figure 10

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=4.0, a4=10.0, Δ=0.05

Choosing a1=0.4, a2=0.6, a3=3.5, a4=7.0, then a2>a1 and (a2a1)a4<a3<a2a4, which implies the existence of equilibria E1 and E2. Using the conditions of local stability, we get tumor-free equilibrium E1 as unstable and co-axial equilibrium E2 as stable in nature. From Figs. 11 and 12, we observe a stability switch in the system (2.2) as the delay factor Δ crosses a threshold.

Figure 11.

Figure 11

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.4, a2=0.6, a3=3.5, a4=7.0, Δ=0.01

Figure 12.

Figure 12

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.4, a2=0.6, a3=3.5, a4=7.0, Δ=0.05

Choosing a1=0.4, a2=0.6, a3=3.5, a4=7.0, then a2>a1 and 0<a3<(a2a1)a4, which indicates the existence of tumor-free equilibrium E1. At this equilibrium the system (2.2) shows unstable behavior. Figures 13 and 14 indicate that the number of tumor cells increases without restriction, which is in accordance with the immune escape phenomena of tumor which is observed clinically.

Figure 13.

Figure 13

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=1.0, a4=5.0, Δ=0.01

Figure 14.

Figure 14

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=1.0, a4=5.0, Δ=0.05

Choosing a1=0.3, a2=0.6, a3=0.5, a4=0.7, then a3>a2a4, which suggests the existence of the stable tumor-free equilibrium E1. Figures 15 and 16 clarify that the tumor-free equilibrium is asymptotically stable, which is in accordance with the spontaneous tumor regression phenomena observed clinically.

Figure 15.

Figure 15

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=0.5, a4=0.7, Δ=0.01

Figure 16.

Figure 16

Time evaluation curve and three-dimensional phase portrait of the system for the parameter values a1=0.3, a2=0.6, a3=0.5, a4=0.7, Δ=0.05

Conclusion

In this paper, we aimed to investigate the dynamical behavior of the modified Pang et al. model [17]. In their model [17], it was shown that with the increase of normal flow rate of mature immune cells, the system exhibits different states such as tumor dormant, periodic tumor oscillation, immune escape of tumor, and so on. However, the effects of the delay term on the oscillatory behavior were not considered in their model. Therefore, a delay term was included in our model, and we investigated the system behavior with varying system parameters. As a result, the modified model showed that the system (2.2) could generate an oscillatory response even with a delay term. Moreover, it illustrated that these oscillations were persistent and could not be destroyed by the additional delay term. Our bifurcation analysis and numerical simulations revealed that a “careful” selection of the model’s parameters must be obtained so that the stable steady-state loses its stability. We showed that the delay term was not necessary to generate oscillations because our model can generate these oscillations even without the delay term. From the bifurcation analysis, in addition to Figs. 9 and 10, it can be shown that Δ neither affects generating of oscillations nor the amplitude of these oscillations. However, varying other parameters such as but not limited to a1, a2 leads to the stabilization of the unstable equilibrium point. A set of realistic parameter values gives us a better insight into the model, which we leave as our future work.

In our entire discussion, the major goal was to have a dynamical analysis of the considered model with the incorporation of a delay term. The numerical results were obtained by applying standard MATLAB software. The aspects of numerical stability, CPU time, minimum error, etc. of the adopted numerical techniques were not investigated. The interested readers and researchers are referred to [36, 37] for such kinds of investigations.

Acknowledgements

The authors of this paper thank both the anonymous reviewers on the basis of whose reports and suggestions the improvement of the paper was possible.

Authors’ contributions

All authors jointly worked on the results, and they read and approved the final manuscript.

Funding

There is no funding for this work.

Availability of data and materials

Not applicable.

Declarations

Competing interests

The authors declare that they have no competing interests.

Contributor Information

Kaushik Dehingia, Email: kaushikdehingia17@gmail.com.

Hemanta Kumar Sarmah, Email: nsarmah@hotmail.com.

Yamen Alharbi, Email: ysoalharbe@kau.edu.sa.

Kamyar Hosseini, Email: kamyar_hosseini@yahoo.com.

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