Home > Publications database > Peptides Derived From Insulin Granule Proteins Are Targeted by CD8+ T Cells Across MHC Class I Restrictions in Humans and NOD Mice. > print |
001 | 167227 | ||
005 | 20240229123235.0 | ||
024 | 7 | _ | |2 doi |a 10.2337/db20-0013 |
024 | 7 | _ | |2 pmid |a pmid:32928873 |
024 | 7 | _ | |2 ISSN |a 0012-1797 |
024 | 7 | _ | |2 ISSN |a 1939-327X |
024 | 7 | _ | |a altmetric:90329746 |2 altmetric |
037 | _ | _ | |a DKFZ-2021-00212 |
041 | _ | _ | |a eng |
082 | _ | _ | |a 610 |
100 | 1 | _ | |a Azoury, Marie Eliane |b 0 |
245 | _ | _ | |a Peptides Derived From Insulin Granule Proteins Are Targeted by CD8+ T Cells Across MHC Class I Restrictions in Humans and NOD Mice. |
260 | _ | _ | |a Alexandria, Va |b Assoc. |c 2020 |
336 | 7 | _ | |2 DRIVER |a article |
336 | 7 | _ | |2 DataCite |a Output Types/Journal article |
336 | 7 | _ | |0 PUB:(DE-HGF)16 |2 PUB:(DE-HGF) |a Journal Article |b journal |m journal |s 1612168957_12223 |
336 | 7 | _ | |2 BibTeX |a ARTICLE |
336 | 7 | _ | |2 ORCID |a JOURNAL_ARTICLE |
336 | 7 | _ | |0 0 |2 EndNote |a Journal Article |
500 | _ | _ | |a Division of Developmental Immunology |
520 | _ | _ | |a The antigenic peptides processed by β-cells and presented through surface HLA class I molecules are poorly characterized. Each HLA variant (e.g., the most common being HLA-A2 and HLA-A3) carries some peptide-binding specificity. Hence, features that, despite these specificities, remain shared across variants may reveal factors favoring β-cell immunogenicity. Building on our previous description of the HLA-A2/A3 peptidome of β-cells, we analyzed the HLA-A3-restricted peptides targeted by circulating CD8+ T cells. Several peptides were recognized by CD8+ T cells within a narrow frequency (1-50/106), which was similar in donors with and without type 1 diabetes and harbored variable effector/memory fractions. These epitopes could be classified as conventional peptides or neoepitopes, generated either via peptide cis-splicing or mRNA splicing (e.g., secretogranin-5 [SCG5]-009). As reported for HLA-A2-restricted peptides, several epitopes originated from β-cell granule proteins (e.g., SCG3, SCG5, and urocortin-3). Similarly, H-2Kd-restricted CD8+ T cells recognizing the murine orthologs of SCG5, urocortin-3, and proconvertase-2 infiltrated the islets of NOD mice and transferred diabetes into NOD/scid recipients. The finding of granule proteins targeted in both humans and NOD mice supports their disease relevance and identifies the insulin granule as a rich source of epitopes, possibly reflecting its impaired processing in type 1 diabetes. |
536 | _ | _ | |0 G:(DE-HGF)POF3-314 |a 314 - Tumor immunology (POF3-314) |c POF3-314 |f POF III |x 0 |
588 | _ | _ | |a Dataset connected to CrossRef, PubMed, |
650 | _ | 7 | |2 NLM Chemicals |a Chromogranins |
650 | _ | 7 | |2 NLM Chemicals |a Epitopes |
650 | _ | 7 | |2 NLM Chemicals |a HLA-A3 Antigen |
650 | _ | 7 | |2 NLM Chemicals |a Insulin |
650 | _ | 7 | |2 NLM Chemicals |a Neuroendocrine Secretory Protein 7B2 |
650 | _ | 7 | |2 NLM Chemicals |a RNA, Messenger |
650 | _ | 7 | |2 NLM Chemicals |a Ucn3 protein, mouse |
650 | _ | 7 | |2 NLM Chemicals |a Urocortins |
650 | _ | 2 | |2 MeSH |a Adult |
650 | _ | 2 | |2 MeSH |a Alternative Splicing |
650 | _ | 2 | |2 MeSH |a Animals |
650 | _ | 2 | |2 MeSH |a CD8-Positive T-Lymphocytes |
650 | _ | 2 | |2 MeSH |a Case-Control Studies |
650 | _ | 2 | |2 MeSH |a Chromogranins: genetics |
650 | _ | 2 | |2 MeSH |a Chromogranins: metabolism |
650 | _ | 2 | |2 MeSH |a Computer Simulation |
650 | _ | 2 | |2 MeSH |a Data Mining |
650 | _ | 2 | |2 MeSH |a Diabetes Mellitus, Type 1: genetics |
650 | _ | 2 | |2 MeSH |a Diabetes Mellitus, Type 1: metabolism |
650 | _ | 2 | |2 MeSH |a Epitopes |
650 | _ | 2 | |2 MeSH |a Female |
650 | _ | 2 | |2 MeSH |a Gene Expression Regulation |
650 | _ | 2 | |2 MeSH |a HLA-A3 Antigen |
650 | _ | 2 | |2 MeSH |a Humans |
650 | _ | 2 | |2 MeSH |a Insulin |
650 | _ | 2 | |2 MeSH |a Male |
650 | _ | 2 | |2 MeSH |a Mice |
650 | _ | 2 | |2 MeSH |a Mice, Inbred NOD |
650 | _ | 2 | |2 MeSH |a Neuroendocrine Secretory Protein 7B2: genetics |
650 | _ | 2 | |2 MeSH |a Neuroendocrine Secretory Protein 7B2: metabolism |
650 | _ | 2 | |2 MeSH |a Protein Binding |
650 | _ | 2 | |2 MeSH |a RNA, Messenger: genetics |
650 | _ | 2 | |2 MeSH |a Urocortins: genetics |
650 | _ | 2 | |2 MeSH |a Urocortins: metabolism |
650 | _ | 2 | |2 MeSH |a Young Adult |
700 | 1 | _ | |a Tarayrah, Mahmoud |b 1 |
700 | 1 | _ | |a Afonso, Georgia |b 2 |
700 | 1 | _ | |a Pais, Aurore |b 3 |
700 | 1 | _ | |a Colli, Maikel L |b 4 |
700 | 1 | _ | |a Maillard, Claire |b 5 |
700 | 1 | _ | |a Lavaud, Cassandra |b 6 |
700 | 1 | _ | |0 0000-0002-4549-699X |a Alexandre-Heymann, Laure |b 7 |
700 | 1 | _ | |a Gonzalez-Duque, Sergio |b 8 |
700 | 1 | _ | |a Verdier, Yann |b 9 |
700 | 1 | _ | |a Vinh, Joelle |b 10 |
700 | 1 | _ | |0 P:(DE-He78)d2f9dbffa7b9a979f9bc4d81e769497e |a Pinto, Sheena |b 11 |
700 | 1 | _ | |a Buus, Soren |b 12 |
700 | 1 | _ | |0 0000-0003-3287-6309 |a Dubois-Laforgue, Danièle |b 13 |
700 | 1 | _ | |0 0000-0002-1017-1845 |a Larger, Etienne |b 14 |
700 | 1 | _ | |a Beressi, Jean-Paul |b 15 |
700 | 1 | _ | |a Bruno, Graziella |b 16 |
700 | 1 | _ | |0 0000-0003-2453-5889 |a Eizirik, Decio L |b 17 |
700 | 1 | _ | |a You, Sylvaine |b 18 |
700 | 1 | _ | |0 0000-0002-9846-8861 |a Mallone, Roberto |b 19 |
773 | _ | _ | |0 PERI:(DE-600)1501252-9 |a 10.2337/db20-0013 |g Vol. 69, no. 12, p. 2678 - 2690 |n 12 |p 2678 - 2690 |t Diabetes |v 69 |x 1939-327X |y 2020 |
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