Human eosinophils exert TNF-α and granzyme A-mediated tumoricidal activity toward colon carcinoma cells

J Immunol. 2010 Dec 15;185(12):7443-51. doi: 10.4049/jimmunol.1000446. Epub 2010 Nov 10.

Abstract

Peripheral blood and tissue eosinophilia is a prominent feature in allergic diseases and helminth infections. In cancer patients, tumor-associated tissue eosinophilia is frequently observed. Tumor-associated tissue eosinophilia can be associated with a favorable prognosis, notably in colorectal carcinoma. However, underlying mechanisms of eosinophil contribution to antitumor responses are poorly understood. We have in this study investigated the direct interactions of human eosinophils with Colo-205, a colorectal carcinoma cell line, and show that eosinophils induce apoptosis and directly kill tumor cells. Using blocking Abs, we found that CD11a/CD18 complex is involved in the tumoricidal activity. Coculture of eosinophils with Colo-205 led to the release of eosinophil cationic protein and eosinophil-derived neurotoxin as well as TNF-α secretion. Moreover, eosinophils expressed granzyme A, which was released upon interaction with Colo-205, whereas cytotoxicity was partially inhibited by FUT-175, an inhibitor of trypsin-like enzymatic activity. Our data present the first demonstration, to our knowledge, that granzyme A is a cytotoxic mediator of the eosinophil protein arsenal, exerting eosinophil tumoricidal activity toward Colo-205, and provide mechanistic evidence for innate responses of eosinophil against tumor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / immunology
  • Antibodies / pharmacology
  • Apoptosis / immunology*
  • Benzamidines
  • CD11a Antigen / immunology
  • CD11a Antigen / metabolism
  • CD18 Antigens / immunology
  • CD18 Antigens / metabolism
  • Cell Line, Tumor
  • Coculture Techniques
  • Colonic Neoplasms / immunology*
  • Colonic Neoplasms / metabolism
  • Eosinophilia / immunology
  • Eosinophilia / metabolism
  • Eosinophils / enzymology*
  • Eosinophils / metabolism
  • Granzymes / immunology*
  • Granzymes / metabolism
  • Guanidines / pharmacology
  • Humans
  • Immunity, Innate*
  • Trypsin Inhibitors / pharmacology
  • Tumor Necrosis Factor-alpha / immunology*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antibodies
  • Benzamidines
  • CD11a Antigen
  • CD18 Antigens
  • Guanidines
  • Trypsin Inhibitors
  • Tumor Necrosis Factor-alpha
  • Granzymes
  • nafamostat