Source:http://linkedlifedata.com/resource/pubmed/id/15889252
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rdf:type | |
lifeskim:mentions |
umls-concept:C0021034,
umls-concept:C0030956,
umls-concept:C0039195,
umls-concept:C0205263,
umls-concept:C0439828,
umls-concept:C0871261,
umls-concept:C1441547,
umls-concept:C1514562,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221,
umls-concept:C2911692
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pubmed:issue |
11
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pubmed:dateCreated |
2005-9-28
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pubmed:abstractText |
The variable domain of immunoglobulin heavy chain (Ig HV) is well-characterized tumor associated antigen expressed in B-cell malignancies, which may function as a T-cell target. However, T-cell epitopes derived from shared framework regions (FRs) of each IgHV subfamily capable of inducing cytotoxic T lymphocytes (CTLs) against the B-cell malignancy, have not been identified. Using the specific PCR primers of seven IgHV gene subfamilies, we amplified the IgHV gene rearrangement for 108 cases of B-cell acute lymphoblastic leukemia (B-ALL) patients. The IgHV gene rearrangement fragments of B-ALL patients were directly sequenced then classified into seven different subfamilies. The T-cell epitopes encoded by the IgHV gene in the B-ALL patients were predicted by SYFPEITHI and BIMAS programs and compared with those from 56 representative germline IgHV sequences in the genebank. For the HLA-A*0201 locus, we found 1 or 2 top score shared epitopes from each subfamily and got 12 epitopes altogether. Results showed that ten of them were in the FRs. Using an antigen-specific T-cell expansion system, we generated the peptide-special CTLs in vitro, which were capable of killing B lymphoma cell lines that belonged to the same IgHV subfamily in a peptide-specific and HLA-restricted manner. Furthermore, we proved that the cytotoxicity of CTLs was IgHV subfamily-specific. These data indicate possible immunotherapy approaches for B-cell malignances patients based on IgHV gene subfamilies.
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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/Epitopes, T-Lymphocyte,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-A Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Heavy Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Variable Region,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0340-7004
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1106-14
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15889252-Burkitt Lymphoma,
pubmed-meshheading:15889252-Cell Line, Tumor,
pubmed-meshheading:15889252-Cytotoxicity, Immunologic,
pubmed-meshheading:15889252-Epitopes, T-Lymphocyte,
pubmed-meshheading:15889252-Gene Rearrangement,
pubmed-meshheading:15889252-Genes, T-Cell Receptor beta,
pubmed-meshheading:15889252-HLA-A Antigens,
pubmed-meshheading:15889252-Humans,
pubmed-meshheading:15889252-Immunoglobulin Heavy Chains,
pubmed-meshheading:15889252-Immunoglobulin Variable Region,
pubmed-meshheading:15889252-Peptide Fragments,
pubmed-meshheading:15889252-T-Lymphocytes, Cytotoxic
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pubmed:year |
2005
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pubmed:articleTitle |
Induction of anti B-cell malignance CTL response by subfamily-shared peptides derived from variable domain of immunoglobulin heavy chain.
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pubmed:affiliation |
Department of Hematology, Peking University First Hospital, No. 8, Xishiku Street, West District, Beijing 100034, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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