[1] 孙奇. IL-22-炎症性疾病关键因子. 免疫学杂志,2011,9(2):221-223. [2] 晁康,龚晓蓉,陈旻湖,等. Th17细胞在肝脏疾病中的免疫病理作用. 实用肝脏病杂志,2010,6(3):465-468. [3] Guabiraba R,Besnard A G,Marques R E,et al. IL-22 modulates IL-17A production and controls inflammation and tissue damage in experimental dengue infection. Eur J Immunol,2013,43(6):1529-1544. [4] Zenewicz L A,Flavell R A. Recent advances in IL-22 biology. Int Immunol,2011,23(3):159-163. [5] Ogata H,Chinen T,Yoshida T,et al. Loss of SOCS3 in the liver promotes fibrosis by enhancing STAT3-mediated TGF-beta1 production. Oncogene,2006,25(17):2520-2530. [6] Alexander WS,Hilton DJ. The role of suppressors of cytokine signaling(SOCS) proteins in regulation of the immune response. Annu Rev Immunol,2004,22:503-529. [7] Jo D, Liu D,Yao S,et al.Intracellular protein therapy with SOCS3 inhibits inflammation and apoptosis. Nat Med,2005,11(8): 892-898. [8] Koeberlein B,zur Hausen A,Bektas N,et al. Hepatitis B virus overexpresses suppressor of cytokine signaling-3(SOCS3) thereby contributing to severity of inflammation in the liver. Virus Res,2010,148(1-2):51-59. [9] Ogata H,Kobayashi T,Chinen T,et al. Deletion of the SOCS3 gene in liver parenchymal cells promotes hepatitis-induced hepatocarcinogenesis. Gastroenterology,2006,131(1):179-193. [10] Okada S,Nakamura M,Katoh H,et al. Conditional ablation of Stat3 or Socs3 discloses a dual role for reactive astrocytes after spinal cord injury. Nat Med,2006,12(7):829-834. [11] Wolk K,Sabat R. Interleukin-22: a novel T- and NK-cell derived cytokine that regulates the biology of tissue cells. Cytokine Growth Factor Rev,2006,17(5):367-380. [12] Feng D. Interleukin-22,liver progenitor cells,and liver cancer. Hepatology,2013,accepted Article(Accepted,unedited articles published online and citable. The final edited and typeset version of record will appear in future.) [13] Cobleigh M A,Robek M D. Protective and pathological properties of IL-22 in liver disease:implications for viral hepatitis. Am J Pathol,2013,182(1):21-28. [14] Radaeva S,Sun R,Pan HN,et al. Interleukin 22(IL-22) plays a protective role in T cell-mediated murine hepatitis:IL-22 is a survival factor for hepatocytes via STAT3 activation. Hepatology,2004,39(5):1332-1342. [15] Xiang X,Gui H,King N J,et al. IL-22 and non-ELR-CXC chemokine expression in chronic hepatitis B virus-infected liver. Immunol Cell Biol,2012,90(6):611-619. [16] Hoegl S,Bachmann M,Scheiermann P,et al. Protective properties of inhaled IL-22 in a model of ventilator-induced lung injury. Am J Respir Cell Mol Biol,2011,44(3):369-376. [17] Pickert G,Neufert C,Leppkes M,et al. STAT3 links IL-22 signaling in intestinal epithelial cells to mucosal wound healing. J Exp Med,2009,206(7):1465-1472. [18] Croker B A,Krebs D L,Zhang J G,et al. SOCS3 negatively regulates IL-6 signaling in vivo. Nat Immunol,2003,4(6):540-545. [19] Fischer P,Lehmann U,Sobota R M,et al. The role of the inhibitors of interleukin-6 signal transduction SHP2 and SOCS3 for desensitization of interleukin-6 signalling. Biochem J,2004,378(Pt 2):449-460. [20] Yoshimura A,Ohishi H M M,Aki D,et al. Regulation of TLR signaling and inflammation by SOCS family proteins. J Leukoc Biol,2004,75(3): 422-427. [21] Nagalakshmi M L,Rascle A,Zurawski S,et al. Interleukin-22 activates STAT3 and induces IL-10 by colon epithelial cells. Int Immunopharmacol,2004,4(5):679-691. [22] Zhang W,Dang E,Shi X,et al. The pro-inflammatory cytokine IL-22 up-regulates keratin 17 expression in keratinocytes via STAT3 and ERK1/2. PloS one,2012,7(7):e40797. [23] Brand S,Dambacher J,Beigel F,et al. IL-22-mediated liver cell regeneration is abrogated by SOCS-1/3 overexpression in vitro. Am J Physiol Gastrointest Liver Physiol,2007,292(4):G1019-1028. [24] Liang S C,Tan X Y,Luxenberg D P,et al. Interleukin (IL)-22 and IL-17 are coexpressed by Th17 cells and cooperatively enhance expression of antimicrobial peptides. J Exp Med,2006,203(10):2271-2279. [25] Nakaya M,Hamano S,Kawasumi M,et al.Aberrant IL-4 production by SOCS3-over-expressing T cells during infection with Leishmania major exacerbates disease manifestations. Int Immunol,2011,23(3):195-202. [26] Nakaya M,Hashimoto M,Nakagawa R,et al. SOCS3 in T and NKT cells negatively regulates cytokine production and ameliorates ConA-induced hepatitis. J Immunol,2009,183(11):7047-7053. |