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PMID: 11358432 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cytotoxic T cells to an epitope in the islet autoantigen IA-2 are not disease-specific.

Clinical immunology (Orlando, Fla.) ·Vol. 99 ·No. 3 ·2001-06-00 ·Pages 360-4

Takahashi K, Honeyman MC, Harrison LC

Abstract

Cytotoxic CD8 T lymphocytes (CTL) are effectors of pancreatic islet beta-cell destruction in type 1 diabetes but, with the exception of a single report, CTL to islet antigen peptides have not been identified. We used autologous blood monocyte-derived dendritic cells to elicit HLA-A2-restricted CTL to a peptide, MVWESGCTV (aa 797-805), that is contiguous with a dominant CD4 T-cell epitope in the islet antigen tyrosine phosphatase IA-2. IA-2 peptide-specific CTL activity measured as 51Cr release from autologous lymphoblasts was detected in 2/6 islet antibody-positive relatives at high risk for type 1 diabetes but also in 2/6 closely HLA-matched controls. All subjects had CTL activity to an HLA-A2-restricted Epstein-Barr virus peptide. CTL to the IA-2 self-peptide were therefore not disease-specific, consistent with other evidence that autoreactive T cells are present in healthy individuals.

MeSH Terms
Adolescent Adult Autoantibodies/immunology Child Dendritic Cells/physiology Diabetes Mellitus, Type 1/immunology Epitopes Female HLA-A2 Antigen/metabolism Humans Male Middle Aged T-Lymphocytes, Cytotoxic/immunology
Chemicals
Autoantibodies Epitopes HLA-A2 Antigen ICA512 autoantibody
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Takahashi K
Autoimmunity and Transplantation Division, Royal Melbourne Hospital, Parkville, 3050, Australia.
Honeyman M C
Harrison L C
Article Info
Journal
Clinical immunology (Orlando, Fla.)
Abbr.
Clin Immunol
ISSN
1521-6616
Published
2001-06-00
Pages
360-4
Language
English
Region
United States
NLM ID
100883537
Subset
IM
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