| Literature DB >> 25577193 |
Naoko Okiyama1, Hisanori Hasegawa2, Takatoku Oida3, Shinya Hirata2, Hiroo Yokozeki4, Manabu Fujimoto5, Nobuyuki Miyasaka6, Hitoshi Kohsaka7.
Abstract
It is suggested that polymyositis, an autoimmune inflammatory myopathy, is mediated by autoaggressive CD8 T cells. Skeletal muscle C protein is a self-antigen that induces C protein-induced myositis, a murine model of polymyositis. To establish a new murine model of myositis inducible with a single CD8 T-cell epitope peptide that derives from the C protein, three internet-based prediction systems were employed to identify 24 candidate peptides of the immunogenic fragment of the C protein and bind theoretically to major histocompatibility complex class I molecules of C57BL/6 (B6) mice. RMA-S cell assay revealed that a HILIYSDV peptide, amino acid position 399-406 of the C protein, had the highest affinity to the H2-K(b) molecules. Transfer of mature bone marrow-derived dendritic cells pulsed with HILIYSDV induced myositis in naive B6 mice. This myositis was suppressed by anti-CD8-depleting antibodies but not by anti-CD4-depleting antibodies. Because this myositis model is mediated by CD8 T cells independently of CD4 T cells, it should be a useful tool to investigate pathology of polymyositis and develop therapies targeting CD8 T cells. © The Japanese Society for Immunology. 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: CD4 T cell; RMA-S cell; bone marrow-derived dendritic cell
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Year: 2015 PMID: 25577193 DOI: 10.1093/intimm/dxv001
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823