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Table 1 Definitions of the parameters used in the model

From: Personalized life expectancy and treatment benefit index of antiretroviral therapy

Variables

Definitions

Initial

Reference

T

Uninfected CD 4+ cell population size

1200 μ l −1

 

T

Infected CD 4+ helper cell population size

0

 

V I

HIV population size

100 μ l −1

 

τ

Prolonged LE

interim variable

 

Parameters

 

baseline values [ranges]

 

s

Rate of supply of CD 4+ T cell from precursors

15 μ l −1 day −1

[21]

d

Death rate of uninfected CD 4+ T cells

0.02 day −1

[21]

\(k(\bar {k})\)

Infection rate per virion

2.1818×10−7 μ l −1 day −1(lk)

[21]

δ

Death rate of infected CD 4+ T cells

0.35 day −1[0.2 0.6]

[21]

\(\lambda (\bar {\lambda })\)

Number of free virus produced by lysing a CD 4+ T cell

3928.6 μ l −1 day −1(l λ)

[21]

c

Death or clearance rate of free virus

2.4 day −1 [1.5 3.5]

[21]

\(\beta _{k}(\bar {\beta }_{k})\)

Scale parameter of Weibull function

1500(225) [50-2000]

see text

\(\beta _{\lambda }(\bar {\beta }_{\lambda })\)

Scale parameter of Weibull function

200(200) [10-500]

see text

\(\alpha _{k}(\bar {\alpha }_{k})\)

Shape parameter of Weibull function

1.1(1.1) [0.2-2]

see text

\(\alpha _{\lambda }(\bar {\alpha }_{\lambda })\)

Shape parameter of Weibull function

0.04(0.04) [0.005-0.2]

see text

T m

LE since infection without therapy

11 [5,16] ×365 days

[34]

\(\eta (\bar {\eta })\)

Drug efficacy of combination therapy

0.95 [0.5 1] (q η)

[21]

\(\tau _{50}(\bar {\tau }_{50})\)

Drug sensitivity of combination therapy

30 [20, 100] ×365 days (p τ 50)

see text

τ m

Maximum LE after infection

(T d T s )days

T d

Time of natural death

74 ×365 days

[37]

T s

Time to initiate treatment after infection

Determined by B CD4

T r

Time of emergence of drug resistant virus

Random variable in [T s ,T e ]

T e

LE after infection with treatment

In [T m ,T d ]

T 1000

Time to virological failure

Determined by viral loads

B CD4

Baseline CD4 counts to initiate the treatment

350 [100-450]cells/ μ l

d a

Drug adherence rate

90% [50-100%]

  1. where l,p,q are modification factors related to corresponding parameters with l=0.935,p=3,q=1 as baseline values. And \(\bar {k}=lk, \bar {\lambda }=l\lambda \), \(\bar {\tau }_{50}=p\tau _{50}\), \(\bar {\eta }=q\eta \). Note that over bar represents the same parameter but with values corresponding to with ART and/or drug resistance