Source:http://linkedlifedata.com/resource/pubmed/id/10086799
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0021758,
umls-concept:C0023434,
umls-concept:C0033268,
umls-concept:C0054950,
umls-concept:C0080202,
umls-concept:C0085358,
umls-concept:C0185117,
umls-concept:C0205217,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1456796,
umls-concept:C1705984,
umls-concept:C1706438,
umls-concept:C1710548,
umls-concept:C2698600,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
1999-4-15
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pubmed:abstractText |
Phenotypic and functional abnormalities within the residual non-B-cell compartment of B-cell chronic lymphocytic leukaemia (CLL) suggest an interaction between tumour cells and host immune effectors. To explore the possibility of a polarized Th1/Th2 response we have studied CD30 antigen expression and the pattern of cytokine production by purified CLL T cells. Activated T cells from CLL patients showed a significant increase in the expression of CD30 compared to normal controls. Accordingly, high levels of soluble CD30 were detected in supernatants from activated T-cell cultures, as well as in CLL serum samples. Messenger RNA for IL4 was found in both resting and, to a greater extent, in activated CLL T lymphocytes. The latter cells were also capable of releasing IL4. Three-colour immunofluorescence analyses revealed a strong CD30 expression in the CD3+/CD8+/CD28- large granular lymphocyte subset, which is considerably expanded in CLL. Production of IL4, as well as expression and release of CD30 by these T cells, was conclusively demonstrated at the clonal level. These findings document an expansion of a peculiar subset of 'Th2-like' cells in CLL, with an increased IL4 production and CD30 expression and release, that are likely to contribute to both the B-cell accumulation and immune-defects characteristic of this disease.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD30,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0007-1048
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
589-99
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:10086799-Aged,
pubmed-meshheading:10086799-Antigens, CD30,
pubmed-meshheading:10086799-CD8-Positive T-Lymphocytes,
pubmed-meshheading:10086799-Clone Cells,
pubmed-meshheading:10086799-Flow Cytometry,
pubmed-meshheading:10086799-Humans,
pubmed-meshheading:10086799-Interferon-alpha,
pubmed-meshheading:10086799-Interleukin-2,
pubmed-meshheading:10086799-Interleukin-4,
pubmed-meshheading:10086799-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:10086799-Phenotype,
pubmed-meshheading:10086799-RNA, Messenger
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pubmed:year |
1999
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pubmed:articleTitle |
IL4 production and increased CD30 expression by a unique CD8+ T-cell subset in B-cell chronic lymphocytic leukaemia.
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pubmed:affiliation |
Immunopharmacology Division, Advanced Biotechnology Centre, National Institute for Cancer Research, Genoa, Italy. gobbi@unige.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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