Source:http://linkedlifedata.com/resource/pubmed/id/20350610
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2010-8-10
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pubmed:abstractText |
Clinical studies have indicated that HLA-DPB1 functions as a classical transplantation antigen in allogeneic stem cell transplantation. Mismatching for HLA-DPB1 was associated with an increased risk of graft-versus-host disease (GVHD), but also a decreased risk of disease relapse. However, specific HLA-DPB1 mismatches were associated with poor clinical outcome. It was suggested that this unfavorable effect was caused by a difference in immunogenicity between HLA-DPB1 alleles. To analyze whether immunogenicity of HLA-DPB1 mismatches could be predicted based on the presence or absence of specific amino acid sequences we developed a model to generate allo-HLA-DPB1 responses in vitro. We tested in total 48 different stimulator/responder combinations by stimulating CD4(+) T cells from 5 HLA-DPB1 homozygous individuals with the same antigen-presenting cells transduced with different allo-HLA-DPB1 molecules. HLA-DPB1 molecules used for stimulation comprised 76% to 99% of HLA-DPB1 molecules present in different ethnic populations. We show that all HLA-DPB1 mismatches as defined by allele typing resulted in high-frequency immune responses. Furthermore, we show that crossrecognition of different HLA-DPB1 molecules is a broadly observed phenomenon. We confirm previously described patterns in crossrecognition, and demonstrate that a high degree in similarity between HLA-DPB1 molecules is predictive for crossrecognition, but not for immunogenicity.
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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 Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-DP Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-DP beta-Chains,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-DPB1 antigen
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1523-6536
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pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2010 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1282-92
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:20350610-Alleles,
pubmed-meshheading:20350610-CD4-Positive T-Lymphocytes,
pubmed-meshheading:20350610-Cross Reactions,
pubmed-meshheading:20350610-Epitopes, T-Lymphocyte,
pubmed-meshheading:20350610-HLA Antigens,
pubmed-meshheading:20350610-HLA-DP Antigens,
pubmed-meshheading:20350610-HLA-DP beta-Chains,
pubmed-meshheading:20350610-HeLa Cells,
pubmed-meshheading:20350610-Humans,
pubmed-meshheading:20350610-Stem Cell Transplantation,
pubmed-meshheading:20350610-Transduction, Genetic,
pubmed-meshheading:20350610-Treatment Outcome
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pubmed:year |
2010
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pubmed:articleTitle |
HLA-DPB1 mismatching results in the generation of a full repertoire of HLA-DPB1-specific CD4+ T cell responses showing immunogenicity of all HLA-DPB1 alleles.
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pubmed:affiliation |
Department of Hematology, Leiden University Medical Center, Leiden, The Netherlands. c.e.rutten@lumc.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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