English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/59459
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

DC FieldValueLanguage
dc.contributor.authorRodríguez-Caballero, Arancha-
dc.contributor.authorGarcía-Montero, Andrés-
dc.contributor.authorAlmeida, Julia-
dc.contributor.authorOrfao, Alberto-
dc.date.accessioned2012-11-05T11:39:55Z-
dc.date.available2012-11-05T11:39:55Z-
dc.date.issued2007-
dc.identifierdoi: 10.1002/cyto.b.20187-
dc.identifierissn: 1552-4949-
dc.identifiere-issn: 1552-4957-
dc.identifier.citationCytometry Part B - Clinical Cytometry 72B(5): 371-379 (2007)-
dc.identifier.urihttp://hdl.handle.net/10261/59459-
dc.description.abstract[Background]: Despite the key role of memory T-cells specific for human cytomegalovirus (hCMV) in protecting against hCMV-reinfection early after immunodeficiency episodes, the precise characterization and definition of the essential components of a protective CD4 T-cell response still remain to be established. [Methods]: We analyzed by flow cytometry hCMV-specific immune responses driven by peripheral blood antigen-presenting cells (APC) and CD4 memory T-cells at both the cellular and soluble levels, and their cooperation in priming and sustaining the effector function of specific CD8 T cells in adult healthy individuals using a hCMV whole viral lysate stimulatory model. [Results]: Overall, activated T-cells showed a heterogeneous phenotype, with a marked predominance of CD45RA-/CCR7+/- memory CD4+ T-cells. Despite this, cytoplasmic expression of granzyme B was found in both the CD45RA+/effector and CD45RA-/memory T-cell compartments of the two major CD4+ and CD8+ activated T-cell subpopulations, further confirming the presence of circulating antigen experienced cytotoxic CD4+ T cells in hCMV-seropositive individuals. Moreover, we observed that both CD4+ and CD8+ hCMV-specific T-cells included relatively restricted numbers of TCR-Vβ family members. Interestingly, we found a significant association between some HLA Class II and Class I haplotypes and the presence of specifically expanded TCR-Vβ clones of anti-hCMV T cells. [Conclusions]: These results indicate that hCMV-specific memory T-cells are phenotypically heterogeneous, their TCR-Vβ repertoire shaped through the interaction between hCMV epitopes and the HLA haplotype. © 2007 Clinical Cytometry Society.-
dc.description.sponsorshipMinisterio de Ciencia y Tecnología, Spain; Grant number: SAF2002-03096; Ministerio de Sanidad y Consumo, Spain; Grant numbers: FIS 02/1244, FIS 05/0399, CP03/00035 and RETICS RD06/0020/0035; Consejería de Educación y Cultura, Junta de Castilla y León, Spain; Grant number: SA 103/03.-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.rightsclosedAccess-
dc.titleAssociation between the HLA haplotype and the TCR-Vβ repertoire of anti-hCMV specific memory T-cells in immunocompetent healthy adults-
dc.typeartículo-
dc.identifier.doi10.1002/cyto.b.20187-
dc.date.updated2012-11-05T11:39:55Z-
dc.description.versionPeer Reviewed-
Appears in Collections:(IBMCC) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
View/Open
Show simple item record
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.