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Cutting Edge: IL-15-Independent NK Cell Response to Mouse Cytomegalovirus Infection
Author(s) -
Joseph C. Sun,
Averil Ma,
Lewis L. Lanier
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0901872
Subject(s) - biology , immunology , cytolysis , interleukin 12 , interleukin 21 , cytokine , secretion , cytomegalovirus , virology , virus , t cell , immune system , cytotoxicity , cytotoxic t cell , endocrinology , herpesviridae , in vitro , viral disease , biochemistry
NK cells respond rapidly during viral infection. The development, function, and survival of NK cells are thought to be dependent on IL-15. In mice lacking IL-15, NK cells are found in severely decreased numbers. Surprisingly, following infection of IL-15- and IL-15Ralpha-deficient mice with mouse CMV, we measured a robust proliferation of Ly49H-bearing NK cells in lymphoid and nonlymphoid organs capable of cytokine secretion and cytolytic function. Remarkably, even in Rag2(-/-) x Il2rg(-/-) mice, a widely used model of NK cell deficiency, we detected a significant number of NK cells 1 wk after mouse CMV infection. In these mice we measured a >300-fold expansion of NK cells, which was dependent on recognition of the m157 viral glycoprotein ligand and IL-12. Together, these findings demonstrate a previously unrecognized independence of NK cells on IL-15 or other common gamma signaling cytokines during their response against viral infection.

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