1. Introduction
Human immunodeficiency virus (HIV) infection as the cause of AIDS has attracted the attention of many researchers from various fields around the world since the 1980s. In particular, the interest of many scientists has been focused on the elaboration and studies of mathematical models which describe the immunological response to infection with HIV. There are different types of such dynamical models that characterize interactions of HIV with
-expressing cells including helper
T cells, macrophages, and natural killer cells. The basic studies in this area are contained in seminal works of [
1,
2,
3,
4,
5]. The mentioned researches were continued in papers [
6,
7,
8,
9,
10,
11,
12,
13,
14] where various dynamical issues related to HIV models are explored, such as positive invariance properties, boundedness of positive half trajectories of this model, stability analysis of equilibrium points, the existence of an orbitally asymptotically stable periodic solution, and bifurcations. These articles did not address the propensity of viral mutations to replicate HIV. Taking HIV mutations into account gives a more realistic picture of the human infectious process. This leads to more complete and complex models. However, as far as the authors know, HIV models with mutant infection have not been sufficiently studied yet [
15,
16,
17,
18,
19,
20,
21,
22].
In [
16], Stengel constructed the seven-order model of HIV mutant infection and discussed the feasibility and effectiveness of the optimal therapies for his model in which virtual therapies for wild-type infections are incorporated:
where the notation
is utilized. The model (
5) has been obtained from 4D equations in [
3] by adding equations describing the dynamics of the mutant HIV strain. The four state variables of the initial model of [
3] represent concentrations of free, wild-type HIV particles (
), uninfected Th cells (
), latently infected Th cells (
), and productively infected Th cells (
) in both the periphery and lymphoid organs. Other state variables of (
1) represent concentrations of the mutant HIV strain (
), proviral Th cells infected by the mutant strain (
), and Th cells productively infected by the new strain (
).
Parameters have the following biological meanings: is the death rate of free virions; is the rate at which CD4 T cells become infected by free virions; is the number of free virions produced by cells; is the death rate of the actively infected CD4 T cell population; is the source term for uninfected CD4 T cells; is the death rate of the uninfected CD4 T cell population; is the growth rate for the CD4 T cell population; is the maximum CD4 T cell population level; is the rate at which cells convert to actively infected cells; is the mutation rate; is the fitness of the mutant strain.
In [
23], it is indicated that the main damage to the immune system occurs in the first weeks of infection, when the diversity of virions is low. The model in [
16] describes the interaction of the HIV-immune system only at an early stage of infection, when wild-type virions and virions of the first mutant strain attack the patient, but new mutant strains have not yet appeared.
Treatment or control parameters
are supposed to be constant,
, and are defined as follows: they are concentrations of protease inhibitor (
), fusion inhibitor (
), Th cell enhancer (
), and reverse transcription inhibitor (
). According to Equation (
1), applied therapy can affect wild HIV particles, but do not possess direct effects on the mutant HIV strain. Stengel raised the question of whether the complex interactions described in the upper three equations of (
1), as well as the presence of the mutant HIV strain variable in the second equation, may have a “good effect” on the patient’s health. Based on clinical practice, according to which “HIV infection is never cured, and requires continuous treatment to maintain a state in remission”, Stengel studied the possibility of optimal therapy for treating HIV infection at certain parameter values. Mathematically, his research is based on the steepest descent algorithm and Pontryagin’s maximum principle.
The purpose of our work is to investigate some qualitative features of the model (
1). Our research provides a positive answer to Stengel’s question for certain ranges of parameter values within the broad framework of the rigorous dynamic analysis (
1) carried out in this article. With this goal, we find equilibrium points and provide local asymptotic stability (LAS) conditions for the infection-free equilibrium point, prove the existence of the attracting set, and calculate ultimate upper bounds for the polytope containing the attracting set. Further, we show that the dynamics of the model (
1) theoretically makes it possible to eradicate the infection by an appropriate choice of treatment parameters if the model parameters satisfy a number of algebraic inequalities. Namely, we find the curious dynamic property of (
1), which is that the LAS conditions of the infection-free equilibrium point imply its global asymptotic stability (GAS) conditions, that is, these GAS conditions cannot be improved. Another interesting issue found here is that these conditions do not depend on controls
and
. Moreover, we describe the case when these conditions do not depend on rest controls
and
as well.
The ranges of parameters at which the cure is achieved in the studied model can be considered as target ranges for real biomedical problems, as well as when choosing parameter control. The biological feasibility issues of numerical values are not the focus of this study.
Biologically, the global asymptotic eradication of infection (GAS) property means that after a sufficiently long observation period, concentrations of wild and mutant HIV particles and infected cells are maintained at a fairly low level. Thus, the results of our study may be applicable in subsequent studies in the case of early initiation of therapy for the patient, when the time period after infection is short.
Our research is based on the localization method of compact invariant sets (LMCIS) [
24], and the LaSalle theorem. It should be noted that earlier, the LMCIS was effectively used in the study of many models taken from chaos theory, see, for example [
25], cosmology [
26], mathematical oncology [
27,
28], mathematical inclusions [
29], and others.
The structure of this paper is the following. In
Section 2 we describe the LMCIS which is utilized in combination with the LaSalle theorem for obtaining conditions for the locations of
-limit sets in coordinate planes.
Section 3 contains preliminary remarks. In
Section 4, formulas for equilibrium points and LAS conditions for the infection-free equilibrium point
are provided. In
Section 5 we derive ultimate upper bounds for all state variables; these bounds define the localization polytope containing the attracting set.
Section 6 contains main results of this paper: we present the GAS conditions, and, besides, we concern two other issues of ultimate dynamics of (
1). Finally, concluding remarks are given in
Section 7.
4. Equilibrium Points
Firstly, in order to find equilibrium points, we eliminate variables
,
,
,
using equations
. As a result, we get the system:
with
Then we come to two cases: (1)
; (2)
. In the first case, we obtain the system
It follows from the second equation that either
or
. If
, then
and we obtain the equilibrium point
with
If
then
and we get the equation respecting
:
Its maximal root is given by
where
We notice that
, provided
.
As a result, we come to the equilibrium point
given by the formula
if
and
.
In the second case
, we derive that
In that way, we come to the system of equations
with respect to
,
Eliminating
we obtain the first equation in the form
where
We come to the equation
This equation has the unique positive root of the form
This solution gives us the equilibrium point
The equilibrium point
if conditions
are fulfilled.
Example 1. Let us select the following set of parameters:Then the system (6) has three equilibrium points: Now we find the stability condition of
. The Jacobian matrix taken at
has the following form:
where by * we denote non-essential elements of
.
The spectrum of the matrix
contains one evident eigenvalue
and eigenvalues of the matrix
which has the block-triangular form:
Therefore, the spectrum of
is the union of spectra of matrices
Both matrices
and
are matrices of the following special type
where all
and
are positive. The characteristic polynomial (with an opposite sign) of the matrix
A has the form
One can show (for instance, using the Hurwitz criterion) that roots of
are negative if, and only if
Hence, the condition (
8) is the stability condition of the matrix
A.
Coming back to matrices
,
we write the stability condition of
in the form:
or in notations (
7) we obtain the condition
In particular,
is LAS with
,
, which means that
,
are contained in the half-space
.
5. Ultimate Upper Bounds
In this section, we derive upper bounds for the dynamics of the system (
4) in nonnegative orthant. Upper bounds give us ultimate maximal values for all cell populations involved into the model. We construct a polytope containing all compact invariant sets in
. This polytope is a positively invariant set and, therefore, limits biologically significant bounded dynamics. Moreover, the polytope turns out to be globally attractive, so all semi-trajectories are bounded as
, and their
-limit sets are contained in the polytope.
Now we demonstrate that this polytope can be constructed by using linear localizing functions.
1. Firstly, we apply the function
. Then
(we recall that
is the Lie derivative of
h with respect to
f) and the set
is defined by
The last formula can be rewritten as
where
The Equation (
10) is quadratic, respecting
, and its larger root increases while
decreases and the left summand increases. Thus,
The value of is reached at the maximum values of the variables , , , , , . We see that . Thus, we get the localizing set .
2. Let us take the next function
. Then
Applying the change
in the equation
, describing the set
, we get that
Solving this linear equation respecting
, we obtain that
with
It follows from (
12) that
and
The fractional linear function (
13) is monotonic within
and we derive that
This estimate can be improved if we use the value
in (
13) instead of
.
Thus, we get the localization set
. Therefore, we come to the estimate
3. Let us apply the localization function
. In this case, the set
is given by
that entails
Hence, we obtain the localization set defined by
4. Let us employ the localization function
. The set
is defined by
Thus, we obtain the localization set defined by
5. Next, let us utilize the localization function
. Then
The set
is defined by
where
Consequently, we have on
that
As a result, we derive that
Therefore, we have the localization set
which provides the bound for
:
6. Now we take the localization function
. Then the set
is given by
Taking into account the bound for
, we get that
7. Now we take the localization function
. The set
is defined by the equation
Using bounds
;
, we get the localizing set
Remark 1. The formula provides the best upper bound for the concentration of uninfected Th cells. Indeed, it was established that and, at the same time, is the coordinate of an equilibrium point. We see that the bound is not refinable.
To summarize all these results, we arrive at:
Theorem 1. All compact invariant sets of the system (4) located in are contained in the polytopeas well. Here, Remark 2. Based on this theorem, we obtain the lower bound for :with 6. On the Location of -Limit Sets
It follows from Theorem 1 that all
-limit sets are located in
. Generally speaking, this polytope is not a positive invariant domain. Let us take a smaller polytope
defined by
We recall that this polytope is the localization set obtained as a result of applying the iterative procedure using localizing functions
, …,
. Herewith, we note that
, with
x taken from the domain
and other inequalities are satisfied. Indeed,
in this domain keeps its sign, and one can verify that for large values of
, the Lie derivative
is negative. This conclusion means that the vector field
f is directed inward
on the boundary of
, and this polytope is positively invariant.
Actually, one can prove a stronger assertion. Arguing as above, we conclude that for any
, the polytope
defined by inequalities
is positively invariant. It follows from this fact that a trajectory exiting a point
, remains in the polytope
for sufficiently large
C. However,
is a compact set. Therefore, the
-limit set of the trajectory is a compact set belonging to
. We conclude that
is a globally attracting set.
Theorem 2. If conditions (9) hold for the system (4), then the equilibrium point attracts all trajectories in . Proof. Let us take the function
with positive parameters
,
. Then we compute that
The condition
holds if the system of inequalities
holds in this polytope, that is, under the condition
.
Excluding parameters
,
, we come to the system
Next, we exclude
:
Finally, we come to the inequalities
which are equivalent to inequalities (
9).
Thus, if inequalities (
9) hold, then the system (
14) has a solution
,
. Taking these values, we have
in polytope
and
if
that is, on the axis
. The unique compact invariant contained in the half axis
is the equilibrium point
. Now our assertion is followed from the LaSalle theorem. □
Remark 3. - 1.
Conditions of Theorem 2 do not depend on controls and .
- 2.
If the condition holds, then Theorem 2 is true. Indeed, taking into account (3), we get that this condition implies the condition and, consequently, conditions (9). Note that the condition does not depend on controls, that is, it is satisfied with zero values of controls.
Theorem 3. Suppose thatThen all ω-limit sets in are located in the invariant plane . Proof. We take
. Then
We obtain
in
if the following conditions hold:
These inequalities have a solution with respect to
,
if the following condition holds:
Since the last inequality is satisfied in virtue of (
17), then for the corresponding choice of parameters
,
, we have that
in
and
if
. Similarly, arguing as in the previous result, we get the desirable conclusion. □
Proof. Let us suppose that
and take the localizing function
with some positive parameters
,
. We calculate that
and estimate this expression within the positively invariant set
. In order to have
in
, we should claim that
Conditions (
20) are met with the appropriate choice of
if the condition (
19) is true. Therefore, choosing the proper parameters
, we have that
within
and
if
therein. Next, all trajectories eventually go into
and remain there. Utilizing the LaSalle theorem with respect to the domain
, we get that all
-limit sets of the system trajectories lie in the plane
.
However, there is only one compact invariant set in the plane
—the equilibrium point
. We conclude that this point is GAS. However, this condition contradicts the condition (
9) of LAS of
. This means that the assumption (
19) is not true, and we have the condition (
18). □
7. Concluding Remarks
In this work, we carry out an analysis of ultimate dynamics of the seven-order Stengel model as mentioned below:
Calculate equilibrium points;
Present local stability conditions;
Find ultimate upper bounds for all variables of this model that define the polytope containing all -limit sets.
Our principal contribution is the exploration of wild-type and the possibility of mutant HIV particle eradication, as well as infected cells in the model (
1) at the early stage of HIV infection provided the treatment affects only wild-type HIV viruses.
In particular, we establish that the LAS condition to the infection-free equilibrium point implies the GAS condition to . These conditions do not depend on control parameters , and under the additional assumption that , the GAS conditions to do not depend on controls , , thus, they can be chosen as equal to zero.
To summarize, the system (
4) may possess complex behaviour only when conditions (
9) are violated. In this case, the location of the attracting set is described in Theorem 1. However, analysis of other features of ultimate dynamics of (
4) remains a very difficult task.