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The journal of immunology : official journal of the American Association of Immunologists v.198 no.3, 2017년, pp.1320 - 1333   SCI SCIE
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IL-15 Enables Septic Shock by Maintaining NK Cell Integrity and Function

Guo, Yin ; Luan, Liming ; Patil, Naeem K. ; Wang, Jingbin ; Bohannon, Julia K. ; Rabacal, Whitney ; Fensterheim, Benjamin A. ; Hernandez, Antonio ; Sherwood, Edward R. ;
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    Interleukin 15 is essential for the development and differentiation of NK and memory CD8 + (mCD8 + ) T cells. Our laboratory previously showed that NK and CD8 + T lymphocytes facilitate the pathobiology of septic shock. However, factors that regulate NK and CD8 + T lymphocyte functions during sepsis are not well characterized. We hypothesized that IL-15 promotes the pathogenesis of sepsis by maintaining NK and mCD8 + T cell integrity. To test our hypothesis, the pathogenesis of sepsis was assessed in IL-15–deficient (IL-15 knockout, KO) mice. IL-15 KO mice showed improved survival, attenuated hypothermia, and less proinflammatory cytokine production during septic shock caused by cecal ligation and puncture or endotoxin-induced shock. Treatment with IL-15 superagonist (IL-15 SA, IL-15/IL-15Rα complex) regenerated NK and mCD8 + T cells and re-established mortality of IL-15 KO mice during septic shock. Preventing NK cell regeneration attenuated the restoration of mortality caused by IL-15 SA. If given immediately prior to septic challenge, IL-15–neutralizing IgG M96 failed to protect against septic shock. However, M96 caused NK cell depletion if given 4 d prior to septic challenge and conferred protection. IL-15 SA treatment amplified endotoxin shock, which was prevented by NK cell or IFN-γ depletion. IL-15 SA treatment also exacerbated septic shock caused by cecal ligation and puncture when given after the onset of sepsis. In conclusion, endogenous IL-15 does not directly augment the pathogenesis of sepsis but enables the development of septic shock by maintaining NK cell numbers and integrity. Exogenous IL-15 exacerbates the severity of sepsis by activating NK cells and facilitating IFN-γ production.


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