<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>37(13)</volume><submitter>van Pul L</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Core fucosylation by fucosyltransferase 8 (FUT8) is an important posttranslational modification that impacts components of the immune system. Genetic variations in FUT8 can alter its function and could, therefore, play a role in the antiviral immune response and pathogenesis of HIV-1. This study analysed the effect of a single nucleotide polymorphism (SNP) in FUT8 on the clinical course of HIV-1 infection.&lt;h4>Design/methods&lt;/h4>The effect of SNPs in FUT8 on untreated HIV-1 disease outcome were analysed in a cohort of 304 people with HIV-1 (PWH) using survival analysis. Flow-cytometry was used to determine the effect of SNP on T-cell activation, differentiation and exhaustion/senescence. T-cell function was determined by proliferation assay and by measuring intracellular </pubmed_abstract><journal>AIDS (London, England)</journal><pagination>1959-1969</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10552802</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A genetic variation in fucosyltransferase 8 accelerates HIV-1 disease progression indicating a role for N-glycan fucosylation.</pubmed_title><pmcid>PMC10552802</pmcid><pubmed_authors>Maurer I</pubmed_authors><pubmed_authors>Harskamp AM</pubmed_authors><pubmed_authors>van Dort KA</pubmed_authors><pubmed_authors>Kootstra NA</pubmed_authors><pubmed_authors>van Pul L</pubmed_authors><pubmed_authors>Boeser-Nunnink BDM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A genetic variation in fucosyltransferase 8 accelerates HIV-1 disease progression indicating a role for N-glycan fucosylation.</name><description>&lt;h4>Objectives&lt;/h4>Core fucosylation by fucosyltransferase 8 (FUT8) is an important posttranslational modification that impacts components of the immune system. Genetic variations in FUT8 can alter its function and could, therefore, play a role in the antiviral immune response and pathogenesis of HIV-1. This study analysed the effect of a single nucleotide polymorphism (SNP) in FUT8 on the clinical course of HIV-1 infection.&lt;h4>Design/methods&lt;/h4>The effect of SNPs in FUT8 on untreated HIV-1 disease outcome were analysed in a cohort of 304 people with HIV-1 (PWH) using survival analysis. Flow-cytometry was used to determine the effect of SNP on T-cell activation, differentiation and exhaustion/senescence. T-cell function was determined by proliferation assay and by measuring intracellular </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2026-05-28T11:09:22.213Z</modification><creation>2025-04-04T12:48:48.496Z</creation></dates><accession>S-EPMC10552802</accession><cross_references><pubmed>37598360</pubmed><doi>10.1097/QAD.0000000000003689</doi></cross_references></HashMap>