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Essential Role of NK Cells in IgG Therapy for Experimental Autoimmune Encephalomyelitis

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Journal PLoS One
Date 2013 Apr 12
PMID 23577171
Citations 6
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Abstract

Intravenous immunoglobulin has long been used in treating autoimmune diseases, although mechanisms remain uncertain. Activating Fcγ receptors are receptors of IgG and reported to be essential in intravenous immunoglobulin (IVIG) therapy. Therefore, we hypothesized natural killer (NK) cells, which express abundant activating Fcγ receptors, are the potential cellular target. In experimental autoimmune encephalomyelitis (EAE), we demonstrated that IgG suppressed disease development in intact, but not in NK cell depleted mice. Adoptive transfer of IgG-treated NK cell could protect mice against EAE, and suppressed interferon γ and interleukin 17 production. The percentage of CD4(+)Foxp3(+) regulatory T cells was significantly increased. The increase of regulatory T cells was also observed in IgG-treated EAE mice but not in NK cell depleted mice. In vitro experiments confirmed that IgG-treated NK cells enhanced regulatory T cell induction from naïve CD4(+) T cells. Interestingly, cells from draining lymph nodes produced more interleukin 2 after the adoptive transfer of IgG-treated NK cells. We neutralized interleukin 2 and the induction of CD4(+)Foxp3(+) T cells by IgG-treated NK cells was significantly reduced. To our knowledge, we identified for the first time the critical role of NK cells in the mechanism of IgG-induced induction of Treg cells in treatment of autoimmunity.

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References
1.
Jacobi C, Claus M, Wildemann B, Wingert S, Korporal M, Romisch J . Exposure of NK cells to intravenous immunoglobulin induces IFN gamma release and degranulation but inhibits their cytotoxic activity. Clin Immunol. 2009; 133(3):393-401. DOI: 10.1016/j.clim.2009.09.006. View

2.
Siragam V, Crow A, Brinc D, Song S, Freedman J, Lazarus A . Intravenous immunoglobulin ameliorates ITP via activating Fc gamma receptors on dendritic cells. Nat Med. 2006; 12(6):688-92. DOI: 10.1038/nm1416. View

3.
Hao J, Liu R, Piao W, Zhou Q, Vollmer T, Campagnolo D . Central nervous system (CNS)-resident natural killer cells suppress Th17 responses and CNS autoimmune pathology. J Exp Med. 2010; 207(9):1907-21. PMC: 2931174. DOI: 10.1084/jem.20092749. View

4.
Setoguchi R, Hori S, Takahashi T, Sakaguchi S . Homeostatic maintenance of natural Foxp3(+) CD25(+) CD4(+) regulatory T cells by interleukin (IL)-2 and induction of autoimmune disease by IL-2 neutralization. J Exp Med. 2005; 201(5):723-35. PMC: 2212841. DOI: 10.1084/jem.20041982. View

5.
Xu W, Fazekas G, Hara H, Tabira T . Mechanism of natural killer (NK) cell regulatory role in experimental autoimmune encephalomyelitis. J Neuroimmunol. 2005; 163(1-2):24-30. DOI: 10.1016/j.jneuroim.2005.02.011. View