Matches in SemOpenAlex for { <https://semopenalex.org/work/W1585520472> ?p ?o ?g. }
- W1585520472 abstract "Abstract Background It has been recently demonstrated that CD8+ T-lymphocyte numbers are genetically transmitted in association with the MHC class I region. The present study was designed with the objective of narrowing the region associated with the setting of CD8+ T-lymphocyte numbers in a population of C282Y homozygous hemochromatosis subjects, in whom a high prevalence of abnormally low CD8+ T-lymphocyte counts has been described. Methods The study includes 43 C282Y homozygous subjects fully characterized both phenotypically and genotypically. Clinical characterization includes measurements of iron parameters at diagnosis (transferrin saturation and serum ferritin), total body iron stores and T-cell immunophenotyping determined by flow cytometry. Genetic characterization includes HLA class I alleles (A, B and C) and four additional microsatellite markers (D6S265, D6S2222, D6S105 and D6S2239) spanning 5 Megabases in the 6p21.3 region. Results Eighty-two extended C282Y carrying haplotypes were defined. Single-locus analysis revealed that the HLA-A region was associated with CD8+ T-cell numbers. Multivariate analysis showed that the combinations of the most common HLA-A alleles (HLA-A*03, -A*02 and -A*01) were associated with significantly lower numbers of CD8+ T-lymphocytes (0.30 ± 0.14 × 10 6 /ml), in comparison with subjects carrying only one copy of those alleles (0.46 ± 0.19 × 10 6 /ml) and subjects without any copy of those alleles (0.79 ± 0.15 × 10 6 /ml; p = 0.0001). No differences were observed in CD8+ T-cell counts among control subjects carrying the same combinations of HLA-A alleles (0.47 ± 0.14; 0.45 ± 0.21 and 0.41 ± 0.17 × 10 6 /ml, respectively), therefore not supporting a direct effect of HLA specificity but rather an indirect association with a locus close to HLA-A. Multivariate analysis showed that the combination of the most common HLA-A alleles also have an impact on the clinical expression of HH in terms of iron stores, in males( p = 0.0009). Conclusion The present study provides evidence supporting an inextricable link between extended HLA haplotypes, CD8+ T-lymphocyte numbers and severity of iron overload in hereditary hemochromatosis(HH). It gives additional information to better define a candidate region involved in the regulation of CD8+ T-lymphocyte numbers. A new evolutionary hypothesis concerning the inheritance of the phenotype of low CD8+ T-lymphocyte numbers associated with particular ancestral HLA haplotypes carrying the C282Y mutation and its implication on the clinical heterogeneity of HH is discussed." @default.
- W1585520472 created "2016-06-24" @default.
- W1585520472 creator A5014959441 @default.
- W1585520472 creator A5015978945 @default.
- W1585520472 creator A5019042215 @default.
- W1585520472 creator A5024166650 @default.
- W1585520472 creator A5025477655 @default.
- W1585520472 creator A5039857672 @default.
- W1585520472 creator A5073709432 @default.
- W1585520472 creator A5076312482 @default.
- W1585520472 date "2006-03-01" @default.
- W1585520472 modified "2023-10-15" @default.
- W1585520472 title "A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload" @default.
- W1585520472 cites W113809990 @default.
- W1585520472 cites W1458739045 @default.
- W1585520472 cites W153886182 @default.
- W1585520472 cites W1563111174 @default.
- W1585520472 cites W1606274933 @default.
- W1585520472 cites W1843849758 @default.
- W1585520472 cites W1966778627 @default.
- W1585520472 cites W1971241700 @default.
- W1585520472 cites W1975066221 @default.
- W1585520472 cites W1978969178 @default.
- W1585520472 cites W1990055465 @default.
- W1585520472 cites W1995852762 @default.
- W1585520472 cites W2002605005 @default.
- W1585520472 cites W2005316756 @default.
- W1585520472 cites W2007714718 @default.
- W1585520472 cites W2021722652 @default.
- W1585520472 cites W2033633198 @default.
- W1585520472 cites W2035790484 @default.
- W1585520472 cites W2043364533 @default.
- W1585520472 cites W2046629565 @default.
- W1585520472 cites W2049901623 @default.
- W1585520472 cites W2052060629 @default.
- W1585520472 cites W2058935272 @default.
- W1585520472 cites W2061138314 @default.
- W1585520472 cites W2094142043 @default.
- W1585520472 cites W2098087474 @default.
- W1585520472 cites W2101521630 @default.
- W1585520472 cites W2101920534 @default.
- W1585520472 cites W2103621645 @default.
- W1585520472 cites W2106246130 @default.
- W1585520472 cites W2130000123 @default.
- W1585520472 cites W2133292468 @default.
- W1585520472 cites W2142802999 @default.
- W1585520472 cites W2145799771 @default.
- W1585520472 cites W2160400039 @default.
- W1585520472 cites W2164017889 @default.
- W1585520472 cites W2164698647 @default.
- W1585520472 cites W2320221849 @default.
- W1585520472 cites W2410907837 @default.
- W1585520472 cites W2412922216 @default.
- W1585520472 cites W4240622224 @default.
- W1585520472 doi "https://doi.org/10.1186/1471-2350-7-16" @default.
- W1585520472 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1413516" @default.
- W1585520472 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16509978" @default.
- W1585520472 hasPublicationYear "2006" @default.
- W1585520472 type Work @default.
- W1585520472 sameAs 1585520472 @default.
- W1585520472 citedByCount "34" @default.
- W1585520472 countsByYear W15855204722012 @default.
- W1585520472 countsByYear W15855204722013 @default.
- W1585520472 countsByYear W15855204722014 @default.
- W1585520472 countsByYear W15855204722015 @default.
- W1585520472 countsByYear W15855204722017 @default.
- W1585520472 countsByYear W15855204722019 @default.
- W1585520472 countsByYear W15855204722021 @default.
- W1585520472 crossrefType "journal-article" @default.
- W1585520472 hasAuthorship W1585520472A5014959441 @default.
- W1585520472 hasAuthorship W1585520472A5015978945 @default.
- W1585520472 hasAuthorship W1585520472A5019042215 @default.
- W1585520472 hasAuthorship W1585520472A5024166650 @default.
- W1585520472 hasAuthorship W1585520472A5025477655 @default.
- W1585520472 hasAuthorship W1585520472A5039857672 @default.
- W1585520472 hasAuthorship W1585520472A5073709432 @default.
- W1585520472 hasAuthorship W1585520472A5076312482 @default.
- W1585520472 hasBestOaLocation W15855204721 @default.
- W1585520472 hasConcept C104317684 @default.
- W1585520472 hasConcept C147483822 @default.
- W1585520472 hasConcept C167672396 @default.
- W1585520472 hasConcept C180754005 @default.
- W1585520472 hasConcept C188280979 @default.
- W1585520472 hasConcept C196166836 @default.
- W1585520472 hasConcept C197754878 @default.
- W1585520472 hasConcept C203014093 @default.
- W1585520472 hasConcept C2776590208 @default.
- W1585520472 hasConcept C2908647359 @default.
- W1585520472 hasConcept C3018783601 @default.
- W1585520472 hasConcept C54355233 @default.
- W1585520472 hasConcept C71924100 @default.
- W1585520472 hasConcept C84597430 @default.
- W1585520472 hasConcept C86803240 @default.
- W1585520472 hasConcept C99454951 @default.
- W1585520472 hasConceptScore W1585520472C104317684 @default.
- W1585520472 hasConceptScore W1585520472C147483822 @default.
- W1585520472 hasConceptScore W1585520472C167672396 @default.
- W1585520472 hasConceptScore W1585520472C180754005 @default.
- W1585520472 hasConceptScore W1585520472C188280979 @default.
- W1585520472 hasConceptScore W1585520472C196166836 @default.