Interleukin-15 Activates Human Natural Killer Cells to Clear the Intestinal Protozoan Cryptosporidium

Intracellular protozoans of the genus Cryptosporidium are a major cause of diarrheal illness worldwide, but little is known about the mechanisms that control intestinal infection. We have previously demonstrated interleukin (IL)–15 expression in the intestinal mucosa of seronegative symptomatic volu...

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Veröffentlicht in:The Journal of infectious diseases 2005-10, Vol.192 (7), p.1294-1302
Hauptverfasser: Dann, Sara M., Wang, Heuy-Ching, Gambarin, Kimberly J., Actor, Jeffrey K., Robinson, Prema, Lewis, Dorothy E., Caillat-Zucman, Sophie, White, A. Clinton
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Sprache:eng
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Zusammenfassung:Intracellular protozoans of the genus Cryptosporidium are a major cause of diarrheal illness worldwide, but little is known about the mechanisms that control intestinal infection. We have previously demonstrated interleukin (IL)–15 expression in the intestinal mucosa of seronegative symptomatic volunteers after oral challenge with C. parvum which suggests a role for IL-15 in the control of acute infection. We hypothesize that IL-15 activates an innate cytolytic cell response that contributes to the clearance of initial C. parvum infection. We report here that IL-15 activates peripheral blood mononuclear cells to lyse Cryptosporidium-infected epithelial cells in a dose-dependent manner. Lysis was due to CD3−CD16+CD56+ cells (i.e., natural killer [NK] cells). Furthermore, flow cytometry revealed that IL-15 increased expression of the activation receptor NKG2D on NK cells, particularly among the CD16Hi cytolytically active cells. Major histocompatibility complex class I–related molecules A and B (MICA and MICB), ligands for NKG2D, were increased after infection of epithelial cell lines and human ileal tissue. These data suggest that IL-15 has an important role in activating an NK cell–mediated pathway that leads to the elimination of intracellular protozoans from the intestines, which is a previously unrecognized feature of NK cell function
ISSN:0022-1899
1537-6613
DOI:10.1086/444393