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J. Virol., 10 1996, 7004-7012, Vol 70, No. 10
MC Monaco, WJ Atwood, M Gravell, CS Tornatore and EO Major
The human polyomavirus JC virus (JCV) infects myelin-producing cells in the
central nervous system, resulting in the fatal demyelinating disease
progressive multifocal leukoencephalopathy (PML). JCV-induced PML occurs
most frequently in immunosuppressed individuals, with the highest incidence
in human immunodeficiency type 1-infected patients, ranging between 4 and
6% of all AIDS cases. Although JCV targets a highly specialized cell in the
central nervous system, infection is widespread, with more than 80% of the
human population worldwide demonstrating serum antibodies. A number of
clinical and laboratory studies have now linked the pathogenesis of PML
with JCV infection in lymphoid cells. For example, JCV-infected lymphocytes
have been suggested as possible carriers of virus to the brain following
reactivation of a latent infection in lymphoid tissues. To further define
the cellular tropism associated with JCV, we have attempted to infect
immune system cells, including CD34+ hematopoietic progenitor cells derived
from human fetal liver, primary human B lymphocytes, and human tonsillar
stromal cells. Our results demonstrate that these cell types as well as a
CD34+ human cell line, KG-1a, are susceptible to JCV infection. JCV cannot,
however, infect KG-1, a CD34+ cell line which differentiates into a
macrophage-like cell when treated with phorbol esters. In addition,
peripheral blood B lymphocytes isolated by flow cytometry from a PML
patient demonstrate JCV infection. These results provide direct evidence
that JCV is not strictly neurotropic but can infect CD34+ hematopoietic
progenitor cells and those cells which have differentiated into a
lymphocytic, but not monocytic, lineage.
Copyright © 1996, American Society for Microbiology
JC virus infection of hematopoietic progenitor cells, primary B lymphocytes, and tonsillar stromal cells: implications for viral latency
Laboratory of Molecular Medicine and Neuroscience, National Institute of Neurological Disorders and Stroke, Bethesda, Maryland 20892, USA.
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