Literature DB >> 18358785

Identification of novel IGRP epitopes targeted in type 1 diabetes patients.

Irene Jarchum1, Lynn Nichol, Massimo Trucco, Pere Santamaria, Teresa P DiLorenzo.   

Abstract

CD8(+) T cells play an important role in the development of type 1 diabetes (T1D) in NOD mice and humans. IGRP (islet-specific glucose-6-phosphatase catalytic subunit-related protein) has emerged in recent years as a major antigen in NOD mice. Therefore, we aimed to determine if IGRP is an antigen in T1D patients and to identify the HLA-A2-restricted IGRP epitopes targeted. Using IFN-gamma ELISPOT assay, we tested PBMC from recent-onset pediatric T1D patients and healthy controls for reactivity to four IGRP peptides directly ex vivo. Importantly, 65% of patients and 0% of controls were positive for at least one IGRP peptide. Two of these have not been reported previously. These data provide evidence that IGRP is a CD8(+) T cell antigen in humans, contributing to the understanding of the underlying disease process as well as to future directions for diagnosis and monitoring disease progression in T1D patients.

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Year:  2008        PMID: 18358785      PMCID: PMC2430381          DOI: 10.1016/j.clim.2008.01.015

Source DB:  PubMed          Journal:  Clin Immunol        ISSN: 1521-6616            Impact factor:   3.969


  48 in total

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7.  Efficient culture of CD8(+) T cells from the islets of NOD mice and their use for the study of autoreactive specificities.

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9.  Predominant occupation of the class I MHC molecule H-2Kwm7 with a single self-peptide suggests a mechanism for its diabetes-protective effect.

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