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Journal of Virology, November 2001, p. 10520-10522, Vol. 75, No. 21
Laboratory of Cellular and Molecular
Biophysics, National Institute of Child Health and Human
Development,1 and Laboratory of
Immunoregulation, National Institute of Allergy and Infectious
Diseases,2 National Institutes of Health,
Bethesda, Maryland 20892
Received 22 November 2000/Accepted 1 August 2001
We sought to determine the relationship between virus-mediated
CD4+ T-lymphocyte cytopathicity and viral coreceptor
preference among various human immunodeficiency virus type 1 (HIV-1)
subtypes in an ex vivo-infected human lymphoid tissue model. Our data
show that all R5 HIV-1 infections resulted in mild depletion of
CD4+ T lymphocytes, whereas all X4 HIV-1 infections caused
severe depletion of CD4+ T lymphocytes regardless of their
subtype origin. Thus, at least for the viruses within subtypes A, B, C,
and E that were tested, coreceptor specificity is a critical factor
that determines the ability of HIV-1 to deplete CD4+ T
cells in human lymphoid tissue infected ex vivo.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.21.10520-10522.2001
Human Immunodeficiency Virus Type 1 (HIV-1) Non-B Subtypes
Are Similar to HIV-1 Subtype B in that Coreceptor Specificity Is a
Determinant of Cytopathicity in Human Lymphoid Tissue Infected
Ex Vivo
*
Corresponding author. Mailing address: Bldg. 10, Rm.
6A11, National Institute of Allergy and Infectious Diseases, NIH,
Bethesda, MD 20892-1576. Phone: (301) 402-9015. Fax: (301) 435-3339. E-mail: cwomack{at}niaid.nih.gov.
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