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 atypical 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. (c) 2007 Lippincott Williams & Wilkins.
机构:Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
Kreisberg, JF
;
Yonemoto, W
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机构:Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
Yonemoto, W
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Greene, WC
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Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USAUniv Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
机构:Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
Kreisberg, JF
;
Yonemoto, W
论文数: 0引用数: 0
h-index: 0
机构:Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
Yonemoto, W
;
Greene, WC
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h-index: 0
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Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USAUniv Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA