Source:http://linkedlifedata.com/resource/pubmed/id/18245493
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2008-2-4
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pubmed:abstractText |
EBV-encoded latent membrane protein 1 (LMP1) has oncogenic potential and is expressed in many EBV-associated malignancies. Although LMP1 is regarded as a potential tumor-associated antigen for immunotherapy and several LMP1-specific MHC class I-restricted CTL epitopes have been reported, little is known regarding MHC class II-restricted CD4 helper T-lymphocyte (HTL) epitopes for LMP1. The goal of the present studies was to determine whether MHC class II-restricted CD4 T-cell responses could be induced against the LMP1 antigen and to evaluate the antitumor effect of these responses. We have combined the use of a predictive MHC class II binding peptide algorithm with in vitro vaccination of CD4 T cells using candidate peptides to identify naturally processed epitopes derived from LMP1 that elicit immune responses against EBV-expressing tumor cells. Peptide LMP1(159-175) was effective in inducing HTL responses that were restricted by HLA-DR9, HLA-DR53, or HLA-DR15, indicating that this peptide behaves as a promiscuous T-cell epitope. Moreover, LMP1(159-175)-reactive HTL clones directly recognized EBV lymphoblastoid B cells, EBV-infected natural killer (NK)/T-lymphoma cells and naturally processed antigen in the form of LMP1+ tumor cell lysates presented by autologous dendritic cells. Because the newly identified epitope LMP1(159-175) overlaps with an HLA-A2-restricted CTL epitope (LMP1(159-167)), this peptide might have the ability to induce simultaneous CTL and HTL responses against LMP1. Overall, our data should be relevant for the design and optimization of T-cell epitope-based immunotherapy against various EBV-associated malignancies, including NK/T cell lymphomas.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/EBV-associated membrane antigen...,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes, T-Lymphocyte,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-DR Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Matrix Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1538-7445
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
901-8
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pubmed:meshHeading |
pubmed-meshheading:18245493-Amino Acid Sequence,
pubmed-meshheading:18245493-Antigen Presentation,
pubmed-meshheading:18245493-Burkitt Lymphoma,
pubmed-meshheading:18245493-Cell Line, Tumor,
pubmed-meshheading:18245493-Cell Transformation, Viral,
pubmed-meshheading:18245493-Epitopes, T-Lymphocyte,
pubmed-meshheading:18245493-HLA-DR Antigens,
pubmed-meshheading:18245493-Humans,
pubmed-meshheading:18245493-Jurkat Cells,
pubmed-meshheading:18245493-Killer Cells, Natural,
pubmed-meshheading:18245493-Lymphocyte Activation,
pubmed-meshheading:18245493-Lymphoma, T-Cell,
pubmed-meshheading:18245493-Molecular Sequence Data,
pubmed-meshheading:18245493-Peptide Fragments,
pubmed-meshheading:18245493-T-Lymphocytes,
pubmed-meshheading:18245493-Viral Matrix Proteins
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pubmed:year |
2008
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pubmed:articleTitle |
Induction of EBV-latent membrane protein 1-specific MHC class II-restricted T-cell responses against natural killer lymphoma cells.
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pubmed:affiliation |
Department of Pathology, Asahikawa Medical College, Asahikawa, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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