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http://purl.uniprot.org/citations/37686141http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37686141http://www.w3.org/2000/01/rdf-schema#comment"The human leukocyte antigen (HLA)-B*27 family of alleles is strongly associated with ankylosing spondylitis (AS), a chronic inflammatory disorder affecting the axial and peripheral joints, yet some HLA-B*27 variants not associated with AS have been shown. Since no major differences in the ligandome of associated compared to not-associated alleles have emerged, a plausible hypothesis is that the quantity rather than the quality of the presented epitopes makes the difference. In addition, the Endoplasmic Reticulum AminoPeptidases (ERAPs) 1 and 2, playing a crucial role in shaping the HLA class I epitopes, act as strong AS susceptibility factors, suggesting that an altered peptidome might be responsible for the activation of pathogenic CD8+ T cells. In this context, we have previously singled out a B*27:05-restricted CD8+ T cell response against pEBNA3A (RPPIFIRRL), an EBV peptide lacking the B*27 classic binding motif. Here, we show that a specific ERAP1/2 haplotype negatively correlates with such response in B*27:05 subjects. Moreover, we prove that the B*27:05 allele successfully presents peptides with the same suboptimal N-terminal RP motif, including the self-peptide, pDYNEIN (RPPIFGDFL). Overall, this study underscores the cooperation between the HLA-B*27 and ERAP1/2 allelic variants in defining CD8+ T cell reactivity to suboptimal viral and self-B*27 peptides and prompts further investigation of the B*27:05 peptidome composition."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.org/dc/terms/identifier"doi:10.3390/ijms241713335"xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Molteni E."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Fiorillo M.T."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Sorrentino R."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Congia M."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"D'Abramo M."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Paladini F."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Alba J."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Tuosto L."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Di Franco M."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Cauli A."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Paroli M."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Scrivo R."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Tedeschi V."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Caccavale R."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/author"Paldino G."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/name"Int J Mol Sci"xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/pages"13335"xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/title"ERAP1 and ERAP2 Haplotypes Influence Suboptimal HLA-B*27:05-Restricted Anti-Viral CD8+ T Cell Responses Cross-Reactive to Self-Epitopes."xsd:string
http://purl.uniprot.org/citations/37686141http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/37686141http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/37686141
http://purl.uniprot.org/citations/37686141http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/37686141