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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1988-9-26
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pubmed:abstractText |
The in vitro proliferation capacity of peripheral blood committed T-cell precursors (T-CFC) from LAS patients was studied in order to define whether this parameter could be associated with transition to AIDS. In all patients a significantly (P less than 0.0001) decreased plating efficiency was detected. However, the lowest T-cell colony growth (less than 50 colonies/5 x 10(4) cells) was observed in the 23 patients who subsequently developed the full-blown disease within 150-570 days. Conversely, only one patient (n = 107) whose T-CFC generated greater than 50 colonies/5 x 10(4) cells developed AIDS after a mean follow-up of 867 days (range 120-1260 days). T-CFC from these patients displayed an impaired in vitro differentiation and self-renewal capacity which was independent of the clinical evolution of the disease. In 5 out of 12 AIDS patients, adherent cell-depletion of peripheral blood mononuclear cells (PBMC) enhanced the plating efficiency. Moreover, patients' but not normal adherent cells could inhibit normal T-cell colony growth in a dose-dependent manner. Media conditioned by patients' unstimulated adherent cells (LCM-A+p) also inhibited normal T-cell colony formation. In addition, LCM-A+p were capable of inhibiting interleukin 2-receptor (IL 2-R) expression and interleukin 2 (IL 2) production by normal mitogen-stimulated T-cells. These findings suggest that adherent cell-derived inhibitory activity(ies) could be responsible for the low T-cell colony formation observed in some AIDS patients.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0753-3322
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
21-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3136810-AIDS-Related Complex,
pubmed-meshheading:3136810-Acquired Immunodeficiency Syndrome,
pubmed-meshheading:3136810-Bone Marrow,
pubmed-meshheading:3136810-Hematopoietic Stem Cells,
pubmed-meshheading:3136810-Humans,
pubmed-meshheading:3136810-Interleukin-2,
pubmed-meshheading:3136810-Leukocyte Count,
pubmed-meshheading:3136810-Leukocytes, Mononuclear,
pubmed-meshheading:3136810-Male,
pubmed-meshheading:3136810-Phenotype,
pubmed-meshheading:3136810-Prognosis,
pubmed-meshheading:3136810-Receptors, Immunologic,
pubmed-meshheading:3136810-Receptors, Interleukin-2,
pubmed-meshheading:3136810-T-Lymphocytes,
pubmed-meshheading:3136810-Time Factors
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pubmed:year |
1988
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pubmed:articleTitle |
Prognostic value of blood and bone marrow T-colony-forming cells (T-CFC) in patients with lymphadenopathy syndrome (LAS).
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pubmed:affiliation |
Unité d'Oncogénèse Appliquée (INSERM U 268), Villejuif, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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