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Concordance of CCR5 genotypes that influence cell-mediated immunity and HIV-1 disease progression rates
dc.creator | Catano G. | spa |
dc.creator | Chykarenko Z.A. | spa |
dc.creator | Mangano A. | spa |
dc.creator | Anaya, Juan-Manuel | spa |
dc.creator | He W. | spa |
dc.creator | Smith A. | spa |
dc.creator | Bologna R. | spa |
dc.creator | Sen L. | spa |
dc.creator | Clark R.A. | spa |
dc.creator | Lloyd A. | spa |
dc.creator | Shostakovich-Koretskaya L. | spa |
dc.creator | Ahuja S.K. | spa |
dc.date.accessioned | 2020-05-25T23:56:15Z | |
dc.date.available | 2020-05-25T23:56:15Z | |
dc.date.created | 2011 | spa |
dc.description.abstract | We used cutaneous delayed-type hypersensitivity responses, a powerful in vivo measure of cell-mediated immunity, to evaluate the relationships among cell-mediated immunity, AIDS, and polymorphisms in CCR5, the HIV-1 coreceptor. There was high concordance between CCR5 polymorphisms and haplotype pairs that influenced delayed-type hypersensitivity responses in healthy persons and HIV disease progression. In the cohorts examined, CCR5 genotypes containing -2459G/G (HHA/HHA, HHA/HHC, HHC/HHC) or -2459A/A (HHE/HHE) associated with salutary or detrimental delayed-type hypersensitivity and AIDS phenotypes, respectively. Accordingly, the CCR5-D32 allele, when paired with non-?32-bearing haplotypes that correlate with low (HHA, HHC) versus high (HHE) CCR5 transcriptional activity, associates with disease retardation or acceleration, respectively. Thus, the associations of CCR5-?32 heterozygosity partly reflect the effect of the non-?32 haplotype in a background of CCR5 haploinsufficiency. The correlations of increased delayed-type hypersensitivity with -2459G/G-containing CCR5 genotypes, reduced CCR5 expression, decreased viral replication, and disease retardation suggest that CCR5 may influence HIV infection and AIDS, at least in part, through effects on cell-mediated immunity. © The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. | eng |
dc.format.mimetype | application/pdf | |
dc.identifier.doi | https://doi.org/10.1093/infdis/jiq023 | |
dc.identifier.issn | 00221899 | |
dc.identifier.issn | 15376613 | |
dc.identifier.uri | https://repository.urosario.edu.co/handle/10336/22375 | |
dc.language.iso | eng | spa |
dc.relation.citationEndPage | 272 | |
dc.relation.citationIssue | No. 2 | |
dc.relation.citationStartPage | 263 | |
dc.relation.citationTitle | Journal of Infectious Diseases | |
dc.relation.citationVolume | Vol. 203 | |
dc.relation.ispartof | Journal of Infectious Diseases, ISSN:00221899, 15376613, Vol.203, No.2 (2011); pp. 263-272 | spa |
dc.relation.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-79851475866&doi=10.1093%2finfdis%2fjiq023&partnerID=40&md5=43c0b3b7971702d3bf33fc34343f1805 | spa |
dc.rights.accesRights | info:eu-repo/semantics/openAccess | |
dc.rights.acceso | Abierto (Texto Completo) | spa |
dc.source.instname | instname:Universidad del Rosario | spa |
dc.source.reponame | reponame:Repositorio Institucional EdocUR | spa |
dc.subject.keyword | Chemokine receptor CCR5 | spa |
dc.subject.keyword | Genetic | eng |
dc.subject.keyword | Delayed | eng |
dc.subject.keyword | Cellular | eng |
dc.subject.keyword | CCR5 | eng |
dc.subject.keyword | Virus receptor | spa |
dc.subject.keyword | Acquired immune deficiency syndrome | spa |
dc.subject.keyword | Adult | spa |
dc.subject.keyword | AIDS patient | spa |
dc.subject.keyword | Allele | spa |
dc.subject.keyword | Article | spa |
dc.subject.keyword | Cellular immunity | spa |
dc.subject.keyword | Cohort analysis | spa |
dc.subject.keyword | Controlled study | spa |
dc.subject.keyword | Delayed hypersensitivity | spa |
dc.subject.keyword | Disease course | spa |
dc.subject.keyword | Female | spa |
dc.subject.keyword | Gene expression | spa |
dc.subject.keyword | Genetic association | spa |
dc.subject.keyword | Genetic transcription | spa |
dc.subject.keyword | Genotype | spa |
dc.subject.keyword | Haplotype | spa |
dc.subject.keyword | Heterozygosity | spa |
dc.subject.keyword | Human | spa |
dc.subject.keyword | Human immunodeficiency virus 1 | spa |
dc.subject.keyword | Human immunodeficiency virus 1 infection | spa |
dc.subject.keyword | Human immunodeficiency virus infected patient | spa |
dc.subject.keyword | Immunoregulation | spa |
dc.subject.keyword | In vivo study | spa |
dc.subject.keyword | Major clinical study | spa |
dc.subject.keyword | Male | spa |
dc.subject.keyword | Nucleotide sequence | spa |
dc.subject.keyword | Phenotype | spa |
dc.subject.keyword | Priority journal | spa |
dc.subject.keyword | Single nucleotide polymorphism | spa |
dc.subject.keyword | Virus immunity | spa |
dc.subject.keyword | Virus pathogenesis | spa |
dc.subject.keyword | Virus replication | spa |
dc.subject.keyword | Adult | spa |
dc.subject.keyword | Disease Progression | spa |
dc.subject.keyword | Female | spa |
dc.subject.keyword | Genotype | spa |
dc.subject.keyword | Haplotypes | spa |
dc.subject.keyword | HIV Infections | spa |
dc.subject.keyword | HIV-1 | spa |
dc.subject.keyword | Humans | spa |
dc.subject.keyword | Hypersensitivity | eng |
dc.subject.keyword | Immunity | eng |
dc.subject.keyword | Male | spa |
dc.subject.keyword | Polymorphism | eng |
dc.subject.keyword | Receptors | eng |
dc.title | Concordance of CCR5 genotypes that influence cell-mediated immunity and HIV-1 disease progression rates | spa |
dc.type | article | eng |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | |
dc.type.spa | Artículo | spa |
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