Source:http://linkedlifedata.com/resource/pubmed/id/11167801
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0023418,
umls-concept:C0024264,
umls-concept:C0025260,
umls-concept:C0032659,
umls-concept:C0034790,
umls-concept:C0085358,
umls-concept:C0427526,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1511695,
umls-concept:C1522642,
umls-concept:C1704387,
umls-concept:C1706438,
umls-concept:C1880022,
umls-concept:C2698600
|
pubmed:issue |
1
|
pubmed:dateCreated |
2001-2-22
|
pubmed:abstractText |
Large granular lymphocyte (LGL) leukaemia is a disease with increased numbers of circulating granular lymphocytes and an increased percentage of clonally rearranged CD8(+)CD57(+) cells. To determine whether LGL cells are also found in other lymphocyte subsets, CD8(+) cells from 10 LGL patients were sorted into CD57(+) and CD57(-) fractions and analysed for clonality using a T-cell receptor gamma (TCR gamma) polymerase chain reaction (PCR). In nine patients, a clonal TCR rearrangement was identified in the CD8(+)CD57(+) cells, and in one patient, the TCR rearrangement was oligoclonal in the CD8(+)CD57(+) fraction. In eight out of nine of the clonally rearranged patients, the same band was also present in the CD8(+)CD57(-) fraction. To define the relationship between CD57(-) and CD57(+) LGL populations, CD8(+)CD57(-) and CD8(+)CD57(+) cells were sorted from five patients and cultured in the presence of anti-CD3 plus CD28 antibodies. The CD57(+) cells died of apoptosis before d 7, while the CD57(-) cells proliferated and differentiated into CD57(+) cells. Clonal analysis identified the same band in both cultured subpopulations and in the uncultured CD8(+) cells. Immunophenotypical analysis showed that CD8(+)CD57(-) cells expressed memory cell markers, while the CD8(+)CD57(+) cells exhibited effector characteristics. These results suggest that LGL disease originates in a CD57(-) memory T-cell compartment that continually generates CD57(+) (effector cell) progeny.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0007-1048
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
112
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
189-94
|
pubmed:dateRevised |
2005-11-17
|
pubmed:meshHeading |
pubmed-meshheading:11167801-Adult,
pubmed-meshheading:11167801-Aged,
pubmed-meshheading:11167801-Antigens, CD57,
pubmed-meshheading:11167801-Cell Differentiation,
pubmed-meshheading:11167801-Cells, Cultured,
pubmed-meshheading:11167801-Clone Cells,
pubmed-meshheading:11167801-Female,
pubmed-meshheading:11167801-Flow Cytometry,
pubmed-meshheading:11167801-Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor,
pubmed-meshheading:11167801-Humans,
pubmed-meshheading:11167801-Immunologic Memory,
pubmed-meshheading:11167801-Immunophenotyping,
pubmed-meshheading:11167801-Leukemia, T-Cell,
pubmed-meshheading:11167801-Male,
pubmed-meshheading:11167801-Middle Aged,
pubmed-meshheading:11167801-Polymerase Chain Reaction,
pubmed-meshheading:11167801-T-Lymphocytes, Regulatory
|
pubmed:year |
2001
|
pubmed:articleTitle |
Large granular lymphocyte leukaemia is characterized by a clonal T-cell receptor rearrangement in both memory and effector CD8(+) lymphocyte populations.
|
pubmed:affiliation |
Bone Marrow transplant Unit, Hematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. melenhoj@nih.gov
|
pubmed:publicationType |
Journal Article
|