rdf:type |
|
lifeskim:mentions |
umls-concept:C0029341,
umls-concept:C0034790,
umls-concept:C0086418,
umls-concept:C0205127,
umls-concept:C0871261,
umls-concept:C0936012,
umls-concept:C1515655,
umls-concept:C1527180,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1707391,
umls-concept:C2911692
|
pubmed:issue |
1
|
pubmed:dateCreated |
1997-7-24
|
pubmed:abstractText |
Recent studies have demonstrated biased usage of TCR V beta 17 and a high degree of diversity in J beta usage within the influenza virus matrix epitope (M.58-66)-specific CTL response. In contrast, in the course of a study on the cellular response to influenza A virus, we found preferential usage of V beta 17-J beta 2.2 rearrangement in an individual with an unexpectedly high number of CTL precursors (CTLp). We took advantage of such situation to study the longitudinal repertoire of the CD8+ T cell precursors. By limiting dilution analysis combined with the use of a clonotypic primer corresponding to the CDR3 region of this matrix-specific TCR V beta chain, the influenza-specific CTLp were shown to be stable for a period of 6 years. Overall, our results show that virus-specific CTLp can be directly monitored in vivo by molecular fingerprinting without in vitro restimulation. These findings might be extremely important for evaluation of the specific immune response to a given human pathogen.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/M-protein, influenza virus,
http://linkedlifedata.com/resource/pubmed/chemical/NP protein, Influenza A virus,
http://linkedlifedata.com/resource/pubmed/chemical/Nucleoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Core Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Matrix Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0042-6822
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
23
|
pubmed:volume |
233
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
93-104
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9201219-Animals,
pubmed-meshheading:9201219-Antigens, Viral,
pubmed-meshheading:9201219-Cells, Cultured,
pubmed-meshheading:9201219-Chick Embryo,
pubmed-meshheading:9201219-Cloning, Molecular,
pubmed-meshheading:9201219-Cytotoxicity Tests, Immunologic,
pubmed-meshheading:9201219-Humans,
pubmed-meshheading:9201219-Influenza A virus,
pubmed-meshheading:9201219-Leukocytes, Mononuclear,
pubmed-meshheading:9201219-Longitudinal Studies,
pubmed-meshheading:9201219-Nucleoproteins,
pubmed-meshheading:9201219-Peptides,
pubmed-meshheading:9201219-RNA-Binding Proteins,
pubmed-meshheading:9201219-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:9201219-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:9201219-Viral Core Proteins,
pubmed-meshheading:9201219-Viral Matrix Proteins
|
pubmed:year |
1997
|
pubmed:articleTitle |
In vivo longitudinal analysis of a dominant TCR repertoire selected in human response to influenza virus.
|
pubmed:affiliation |
Institut National de la Santé et de la Recharche Médicale, Unit 445, Paris, France. armelle.prevost_blondel@icgm.cochin.inserm.fr
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|