Determination of simian immunodeficiency virus production by infected activated and resting cells
C Reilly, S Wietgrefe, G Sedgewick, A Haase - Aids, 2007 - journals.lww.com
C Reilly, S Wietgrefe, G Sedgewick, A Haase
Aids, 2007•journals.lww.comObjective: To determine the relative amount of virus produced by activated and resting CD4+
T cells. Design: The total quantity of virus produced by an activated cell relative to a resting
cell in vivo was estimated from 'snap-shots' of virus production by infected cells at one time
point. Methods: Bayesian statistical methods were used to determine a credible interval for
the desired ratio. Results: The posterior mean of the ratio of virus produced by a typical
activated cell to a typical resting cell is 0.82 to 4.28, depending on the half-lives of the resting …
T cells. Design: The total quantity of virus produced by an activated cell relative to a resting
cell in vivo was estimated from 'snap-shots' of virus production by infected cells at one time
point. Methods: Bayesian statistical methods were used to determine a credible interval for
the desired ratio. Results: The posterior mean of the ratio of virus produced by a typical
activated cell to a typical resting cell is 0.82 to 4.28, depending on the half-lives of the resting …
Abstract
Objective:
To determine the relative amount of virus produced by activated and resting CD4+ T cells.
Design:
The total quantity of virus produced by an activated cell relative to a resting cell in vivo was estimated from ‘snap-shots’ of virus production by infected cells at one time point.
Methods:
Bayesian statistical methods were used to determine a credible interval for the desired ratio.
Results:
The posterior mean of the ratio of virus produced by a typical activated cell to a typical resting cell is 0.82 to 4.28, depending on the half-lives of the resting infected cells. Simian immunodeficiency virus-infected resting cells could accordingly be responsible for 70 to 93% of peak virus production in the acute stage of infection.
Conclusions:
Whereas in ‘snap-shots’ the infected resting cells apparently produce much less virus than infected activated CD4+ T cells, the coincidence of peak SIV production with predominant infection of resting cells along with longer half-lives for productively infected resting cells point to a major contribution to virus production in early infection.
Lippincott Williams & Wilkins