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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1997-2-19
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pubmed:abstractText |
The role of T cells in chronic lymphocytic leukemia (CLL) has not been extensively investigated, since the most prominent cellular abnormality in CLL involves the clonal expansion of B cells. In this study we have undertaken a comprehensive analysis of the CD4+ and CD8+ T cell repertoire in a population of CLL patients (n = 19) and age-matched controls (n = 22). The TCR repertoire analysis was performed using a multiplex PCR assay for CDR3 length, an approach that allows for the detection of underlying oligoclonality in complex T cell populations. We established that oligoclonality was substantially more frequent in both the CD4+ and CD8+ T cell populations of CLL patients than in the age-matched controls (p < 0.001). Using three-color FACS analysis with a panel of TCRV segment-specific mAbs, we also established that oligoclonal expansions are predominantly found in the CD57+ subset of both the CD4+ and CD8+ T cell populations. The frequency of the CD57 marker on CD4+ T cells was increased in the setting of CLL (% CD57 = 14.8 +/- 13.0%) compared with that in normal controls (% CD57 = 3.3 +/- 3.0%; p < 0.001). An elevated frequency of CD4+CD57+ T cells was correlated with more advanced disease. Similarly, the most extreme oligoclonal expansions of CD4+CD57+ T cells occurred in CLL patients who had progressed beyond Rai stage 0. These data document profound alterations in the T cell repertoire of CLL patients and point to a role for clonal T cell populations in the pathogenesis of this disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
158
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1482-9
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9013995-Adult,
pubmed-meshheading:9013995-Aged,
pubmed-meshheading:9013995-Amino Acid Sequence,
pubmed-meshheading:9013995-Antigens, CD57,
pubmed-meshheading:9013995-Base Sequence,
pubmed-meshheading:9013995-CD4-Positive T-Lymphocytes,
pubmed-meshheading:9013995-CD8-Positive T-Lymphocytes,
pubmed-meshheading:9013995-Clone Cells,
pubmed-meshheading:9013995-Female,
pubmed-meshheading:9013995-Humans,
pubmed-meshheading:9013995-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:9013995-Male,
pubmed-meshheading:9013995-Middle Aged,
pubmed-meshheading:9013995-Molecular Sequence Data,
pubmed-meshheading:9013995-RNA, Messenger,
pubmed-meshheading:9013995-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:9013995-T-Lymphocyte Subsets
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pubmed:year |
1997
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pubmed:articleTitle |
Clonal expansion within the CD4+CD57+ and CD8+CD57+ T cell subsets in chronic lymphocytic leukemia.
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pubmed:affiliation |
Department of Medicine, North Shore University Hospital/New York University School of Medicine, Manhasset, NY 11030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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