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PMID: 1672165 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Few infected CD4+ T cells but a high proportion of replication-competent provirus copies in asymptomatic human immunodeficiency virus type 1 infection.

Journal of virology ·Vol. 65 ·No. 4 ·1991-04-00 ·Pages 2019-23

Brinchmann JE, Albert J, Vartdal F

Abstract

The virus load in CD4+ T cells from six asymptomatic human immunodeficiency virus type 1 (HIV-1)-infected individuals was determined by limiting-dilution analysis with a sensitive virus isolation procedure and the polymerase chain reaction (PCR). Both methods allowed detection of one HIV-1-infected cell among 10(5) uninfected cells. The number of provirus-containing CD4+ T cells was found to be 1 per 4,000 to 150,000 (median, 1 per 29,000), as determined by virus isolation and 1 per 2,500 to 26,000 (median, 1 per 12,000), as determined by PCR. Infected cells contained an average of 1 to 2 provirus copies, and a high proportion of the provirus copies (1 in 1 to 1 in 6; median, 1 in 2) were replication competent. The results suggest that only a few CD4+ T cells are likely to be lost as a direct consequence of the presence of HIV-1 in infected cells in asymptomatic individuals and that additional mechanisms may contribute to the depletion of CD4+ T cells observed in vivo.

MeSH Terms
Acquired Immunodeficiency Syndrome/diagnosis,immunology,microbiology CD4-Positive T-Lymphocytes/microbiology DNA, Viral/analysis HIV-1/genetics,growth & development Humans Leukocyte Count Polymerase Chain Reaction Proviruses/growth & development Sensitivity and Specificity Virus Replication
Chemicals
DNA, Viral
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brinchmann J E
Institute of Transplantation Immunology, National Hospital, Oslo, Norway.
Albert J
Vartdal F
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22 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1991-04-00
Pages
2019-23
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC240046
Subset
IM
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