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1 December 2004

Volume 190, Number 11
The Journal of Infectious Diseases 2004;190:1989–1997
0022-1899/2004/19011-0015$15.00
DOI: 10.1086/425423
MAJOR ARTICLE

A Model System of Oral HIV Exposure, Using Human Palatine Tonsil, Reveals Extensive Binding of HIV Infectivity, with Limited Progression to Primary Infection

Diane Maher,1

Xiaoyun Wu,3

Timothy Schacker,2

Matthew Larson,2 and

Peter Southern1

Departments of 1Microbiology and 2Medicine, University of Minnesota, Minneapolis; 3Department of Medicine, University of Alabama at Birmingham, Birmingham

Oral exposure to human immunodeficiency virus (HIV) type 1 results in systemic infection, but many details surrounding virus transmission remain unresolved. We developed a mucosal model, using human palatine tonsil with intact external epithelium, to study events after oral exposure to HIV. When applied to the external epithelium, semen from an HIV‐seropositive patient and cell‐free virus both established HIV infection in individual tonsillar cells. However, clusters of infected tonsillar cells were detected where the epithelial surface was damaged. Investigation of the initial events in HIV transmission revealed extensive and stable binding of HIV virions and seminal cells to tonsil epithelium. In experiments modeling physiologically relevant events, the addition of seminal plasma resulted in enhanced virion binding to epithelial cells. These results indicate that, although extensive binding of HIV virions and seminal cells can be demonstrated at an exposed mucosal surface, there is only limited progression from binding to primary infection.

Received 23 March 2004; accepted 17 May 2004; electronically published 3 November 2004.

Reprints or correspondence: Dr. Peter J. Southern, MMC 196, 1460 Mayo, 420 Delaware St., SE, Minneapolis, MN 55455 ().

Cited by

Laurie Gray, Susan Fiscus, Diane Shugars. (2007) HIV-1 Variants from a Perinatal Transmission Pair Demonstrate Similar Genetic and Replicative Properties in Tonsillar Tissues and Peripheral Blood Mononuclear Cells. AIDS Research and Human Retroviruses 23:9, 1095-1104
Online publication date: 1-Oct-2007.
CrossRef
  • Presented in part: Keystone Symposium, HIV‐1 Protection and Control by Vaccination, Keystone, CO, 5–11 April 2002 (abstract 308).

    Financial support: National Institute of Dental and Craniofacial Research (grants DE 12934 and DE 15090); Great Lakes Regional Center for AIDS Research; Microbiology, Immunology, and Cancer Biology Graduate Program, University of Minnesota.

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