TY - JOUR
T1 - Interleukin-15 activates human natural killer cells to clear the intestinal protozoan Cryptosporidium
AU - Dann, Sara M.
AU - Wang, Heuy Ching
AU - Gambarin, Kimberly J.
AU - Actor, Jeffrey K.
AU - Robinson, Prema
AU - Lewis, Dorothy E.
AU - Caillat-Zucman, Sophie
AU - White, A. Clinton
N1 - Funding Information:
Received 1 February 2005; accepted 28 April 2005; electronically published 23 August 2005. Presented in part: Experimental Biology 2004 meeting: “Translating the Genome,” Washington, DC, 17–21 April 2004; 42nd Annual Meeting of the Infectious Diseases Society of America, Boston, September 30–October 3, 2004. Potential conflicts of interest: none reported. Financial support: National Institutes of Health (grant RO1 AI4173); Baylor Center for AIDS Research (grant AI36211). a These authors contributed equally to this study. Reprints or correspondence: Dr. A. Clinton White, Jr., Dept. of Medicine–Infectious Diseases, Baylor College of Medicine, One Baylor Plaza, 535EA, Houston, TX 77030 ([email protected]).
PY - 2005/9/1
Y1 - 2005/9/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=25444486729&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=25444486729&partnerID=8YFLogxK
U2 - 10.1086/444393
DO - 10.1086/444393
M3 - Article
C2 - 16136475
AN - SCOPUS:25444486729
SN - 0022-1899
VL - 192
SP - 1294
EP - 1302
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 7
ER -