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Melanoma inhibitor of apoptosis protein (ML-IAP) specific cytotoxic T lymphocytes cross-react with an epitope from the auto-antigen SS56.

作者信息

Baek Sørensen Rikke, Faurschou Mikkel, Troelsen Lone, Schrama David, Jacobsen Søren, Becker Jürgen C, Thor Straten Per, Andersen Mads Hald

机构信息

Center for Cancer Immune Therapy, Department of Haematology, Herlev University Hospital, Herlev, Denmark.

出版信息

J Invest Dermatol. 2009 Aug;129(8):1992-9. doi: 10.1038/jid.2009.10. Epub 2009 Feb 12.

DOI:10.1038/jid.2009.10
PMID:19212346
Abstract

A large proportion of melanoma patients host a spontaneous T-cell response specifically against ML-IAP-derived peptides. In this study, we describe that some ML-IAP-specific cytotoxic T cells isolated from melanoma patients cross react with an epitope from the auto-antigen SS56. SS56 is a recently described target of autoantibody responses in Sjögren's syndrome (SS) as well as systemic lupus erythematosus (SLE). Here, we describe that SS56 is also an auto-antigen for T cells in SS and SLE. Hence, SS56-specific T cells could readily be detected in circulation and among the infiltrating cells of SLE skin lesions. SS56-specific T cells were able to lyse target cells presenting the peptide epitope on the surface. Notably, SS56-specific CD8 T cells isolated from an SS patient cross reacted with the ML-IAP epitope. This early evidence of a target for auto-reactive CTL in SS and SLE patients; it is to our knowledge previously unreported and underscores the important role of CD8 T cells in autoimmune disorders. Furthermore, the cross-reactivity against the auto-antigen SS56 and the tumor-antigen ML-IAP confirms the link between autoimmunity and anti-cancer cellular immune responses.

摘要

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