Quantitative Image Analysis of HIV-1 Infection in Lymphoid Tissue

Ashley T. Haase(University of Minnesota Medical Center), Keith Henry(University of Minnesota Medical Center), Mary Zupancic(University of Minnesota Medical Center), Gerald Sedgewick(University of Minnesota Medical Center), Russell A. Faust(University of Minnesota Medical Center), Holly Melroe(University of Minnesota Medical Center), Winston Cavert(University of Minnesota Medical Center), Kristin Gebhard(University of Minnesota Medical Center), Katherine Staskus(University of Minnesota Medical Center), Zhi‐Qiang Zhang(University of Minnesota Medical Center), Peter J. Dailey(Omron (Japan)), Henry H. Balfour(University of Minnesota Medical Center), Alejo Erice(University of Minnesota Medical Center), Alan S. Perelson(Los Alamos National Laboratory)
Science
November 8, 1996
Cited by 606

Abstract

Tracking human immunodeficiency virus-type 1 (HIV-1) infection at the cellular level in tissue reservoirs provides opportunities to better understand the pathogenesis of infection and to rationally design and monitor therapy. A quantitative technique was developed to determine viral burden in two important cellular compartments in lymphoid tissues. Image analysis and in situ hybridization were combined to show that in the presymptomatic stages of infection there is a large, relatively stable pool of virions on the surfaces of follicular dendritic cells and a smaller pool of productively infected cells. Despite evidence of constraints on HIV-1 replication in the infected cell population in lymphoid tissues, estimates of the numbers of these cells and the virus they could produce are consistent with the quantities of virus that have been detected in the bloodstream. The cellular sources of virus production and storage in lymphoid tissues can now be studied with this approach over the course of infection and treatment.


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