NK markers are expressed on a high percentage of virus-specific CD8+ and CD4+ T cells

Mark K. Slifka, Robb R. Pagarigan, J. Lindsay Whitton

    Research output: Contribution to journalArticle

    216 Scopus citations


    NK cells have been phenotypically defined by the expression of specific markers such as NK1.1, DX5, and asialo-GM1 (ASGM1). In addition to NK cells, a small population of CD3+ T cells has been shown to express these markers, and a unique subpopulation of NK1.1+ CD3+ T cells that expresses an invariant TCR has been named 'NKT cells.' Here, we describe NK marker expression on a broad spectrum of MHC class I- and MHC class II-restricted T cells that are induced after acute viral infection. From 5 to > 500 days post lymphocytic choriomeningitis virus (LCMV) infection, more than 90% of virus- specific CD8+ and CD4+ T cells coexpress one or more of these three prototypical NK markers. Furthermore, in vivo depletion of NK cells with anti-ASGM1 Ab resulted in the removal of 90% of virus-specific CD8+ T cells and 50-80% of virus-specific CD4+ T cells. This indicates that studies using in vivo depletion to determine the role of NK cells in immune defense could potentially be misinterpreted because of the unintended depletion of Ag- specific T cells. These results demonstrate that NK Ags are widely expressed on the majority of virus-specific T cells and indicate that the NK and T cell lineages may not be as distinct as previously believed. Moreover, the current nomenclature defining NKT cells will require comprehensive modification to include Ag-specific CD8+ and CD4+ T cells that express prototypical NK Ags.

    Original languageEnglish (US)
    Pages (from-to)2009-2015
    Number of pages7
    JournalJournal of Immunology
    Issue number4
    StatePublished - Feb 15 2000

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology

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