Source:http://linkedlifedata.com/resource/pubmed/id/12974795
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rdf:type | |
lifeskim:mentions |
umls-concept:C0019733,
umls-concept:C0032659,
umls-concept:C0085358,
umls-concept:C0152035,
umls-concept:C0205245,
umls-concept:C0205263,
umls-concept:C0449450,
umls-concept:C0796514,
umls-concept:C0871261,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1704632,
umls-concept:C1706438,
umls-concept:C1706817,
umls-concept:C1709269,
umls-concept:C2698600,
umls-concept:C2911692
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pubmed:issue |
4
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pubmed:dateCreated |
2003-9-16
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pubmed:abstractText |
The functional supertype of HLA-A2 was investigated in the presentation of the A*0201-restricted Flu matrix p58-66 peptide to activate recall CD8+ T-cell response. In healthy Northern Chinese, the HLA-A2 supertype was mainly composed of the six alleles, A*0201 (26.4%), A*0206 (12.7%), A*0203 (8.2%), A*0207 (7.3%), A*0210 (1.8%) and A*0205 (0.9%), as analyzed by PCR using sequence specific primer (PCR-SSP) and sequence based typing (SBT). The IFN-gamma release Elispot assay was employed to assess effector CD8+ T cells. In A*0201-bearing individuals, the CD8+ T-cell response was potent when stimulated with autologous CD8- PBMCs. The frequency of the effector CD8+ T cells was 96.6% with the magnitude of effector CD8+ T cells of 225 SFC/5 x 104 CD8+ T cells and the RI of 25.7. In non-A*0201 individuals, the effector CD8+ T cells were minimally detectable while the peptide was presented by the autologous CD8- PBMCs. However, the induction of the response of CD8+ T cells obtained from non-A*0201 individuals was remarkably improved when the peptide was presented by autologous dendritic cells instead of CD8- PBMCs. The HLA-A2 alleles possessing cross-reactivity in the peptide presentation were mainly of A*0206 and non-A*0201 heterozygotes of A*0206 and A*0210. Moreover, A*0206 as the HLA-A2 functional supertype was further confirmed by tetramer assay. In two A*0206+ donors with CD8+ T-cell response to the peptide, the CD8+ T-cell frequency assessed by specific binding of peptide HLA-A*0201 tetramer was 4.62% and 1.66%, respectively. Thus, our results have substantiated the immunological relevance of the HLA-A2 supertype, which may benefit the design of peptide vaccines with the potential to be applicable in broader populations.
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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, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-A2 Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Matrix Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/influenza matrix peptide (58-66)
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0001-2815
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
285-95
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:12974795-Alleles,
pubmed-meshheading:12974795-Antigen Presentation,
pubmed-meshheading:12974795-Antigen-Presenting Cells,
pubmed-meshheading:12974795-Antigens, Viral,
pubmed-meshheading:12974795-Bone Marrow Cells,
pubmed-meshheading:12974795-CD8-Positive T-Lymphocytes,
pubmed-meshheading:12974795-China,
pubmed-meshheading:12974795-Dendritic Cells,
pubmed-meshheading:12974795-HLA-A2 Antigen,
pubmed-meshheading:12974795-Histocompatibility Testing,
pubmed-meshheading:12974795-Humans,
pubmed-meshheading:12974795-Influenza, Human,
pubmed-meshheading:12974795-Influenza A virus,
pubmed-meshheading:12974795-Interferon-gamma,
pubmed-meshheading:12974795-Lymphocyte Activation,
pubmed-meshheading:12974795-Peptide Fragments,
pubmed-meshheading:12974795-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:12974795-Viral Matrix Proteins
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pubmed:year |
2003
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pubmed:articleTitle |
Functional supertype of HLA-A2 in the presentation of Flu matrix p58-66 to induce CD8+ T-cell response in a Northern Chinese population.
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pubmed:affiliation |
Department of Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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