Dendritic cell apoptosis in the maintenance of immune tolerance

Min Chen, Yui-Hsi Wang, Yihong Wang, Li Huang, Hector Sandoval, Yong-Jun Liu, Jin Wang

    Research output: Contribution to journalArticlepeer-review

    291 Scopus citations

    Abstract

    Apoptosis in the immune system is critical for maintaining self-tolerance and preventing autoimmunity. Nevertheless, inhibiting apoptosis in lymphocytes is not alone sufficient to break self-tolerance, suggesting the involvement of other cell types. We investigated whether apoptosis in dendritic cells (DCs) helps regulate self-tolerance by generating transgenic mice expressing the baculoviral caspase inhibitor, p35, in DCs (DC-p35). DC-p35 mice displayed defective DC apoptosis, resulting in their accumulation and, in turn, chronic lymphocyte activation and systemic autoimmune manifestations. The observation that a defect in DC apoptosis can independently lead to autoimmunity is consistent with a central role for these cells in maintaining immune self-tolerance.

    Original languageEnglish (US)
    Pages (from-to)1160-4
    Number of pages5
    JournalScience (New York, N.Y.)
    Volume311
    Issue number5764
    DOIs
    StatePublished - Feb 24 2006

    Keywords

    • Adoptive Transfer
    • Aging
    • Animals
    • Antibodies, Antinuclear
    • Apoptosis
    • Autoimmunity
    • B-Lymphocytes
    • Caspase Inhibitors
    • Cell Survival
    • Dendritic Cells
    • Kidney
    • Lung
    • Lymphocyte Activation
    • Mice
    • Mice, Inbred BALB C
    • Mice, Inbred C57BL
    • Mice, Transgenic
    • Self Tolerance
    • Spleen
    • T-Lymphocytes
    • Viral Proteins
    • Journal Article
    • Research Support, N.I.H., Extramural
    • Research Support, Non-U.S. Gov't

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