4.6 Review

Inherited defects in lymphocyte cytotoxic activity

Journal

IMMUNOLOGICAL REVIEWS
Volume 235, Issue -, Pages 10-23

Publisher

WILEY
DOI: 10.1111/j.0105-2896.2010.00890.x

Keywords

cytotoxicity; hemophagocytic lymphohistiocytic syndrome; IFN-gamma; immunodeficiency disorders; natural mutants; granule exocytosis

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Funding

  1. French National Institute for Health and Medical Research (INSERM)
  2. French National Research Agency
  3. Fondation pour la Recherche Medicale (FRM)
  4. Ministere de l'Education Nationale de la Recherche et de la Technologie and l'Association de Recherche contre le cancer

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The granule-dependent cytotoxic activity of lymphocytes plays a critical role in the defense against virally infected cells and tumor cells. The importance of this cytotoxic pathway in immune regulation is evidenced by the severe and often fatal condition, known as hemophagocytic lymphohistiocytic syndrome (HLH) that occurs in mice and humans with genetically determined impaired lymphocyte cytotoxic function. HLH manifests as the occurrence of uncontrolled activation of T lymphocytes and macrophages infiltrating multiple organs. In this review, we focus on recent advances in the characterization of effectors regulating the release of cytotoxic granules, and on the role of this cytotoxic pathway in lymphocyte homeostasis and immune surveillance. Analysis of the mechanisms leading to the occurrence of hemophagocytic syndrome designates gamma-interferon as an attractive therapeutic target to downregulate uncontrolled macrophage activation, which sustains clinical and biological features of HLH.

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