CpG-activated Thy1.2+ dendritic cells protect against lethal Listeria monocytogenes infection

被引:22
|
作者
Ishii, KJ
Ito, S
Tamura, T
Hemmi, H
Conover, J
Ozato, K
Akira, S
Klinman, DM
机构
[1] US FDA, Sect Retroviral Immunol, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
[2] NICHHD, Lab Mol Growth Regulat, NIH, Bethesda, MD 20892 USA
[3] Osaka Univ, ERATO, Japan Sci & Technol Agcy, Akira Innate Immun Project, Osaka, Japan
[4] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Osaka, Japan
关键词
CpG DNA; innate immunity; host protection; Listeria; TLR9;
D O I
10.1002/eji.200425795
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic oligodeoxynucleotides containing CpG motifs (CpG ODN) activate the innate immune system by interacting with Toll-like receptor 9. The resultant immune response increases host resistance to infection by a variety of pathogenic microorganisms, including Listeria monocytogenes. There is a considerable interest in harnessing the immunoprotective properties of CpG ODN, yet little is known of the cell phenotype(s) responsible for mediating this protection. This work demonstrates that treatment of mice with CpG ODN increases the number of Thy1.2(+), CD11c(+) dendritic cells (Thy1.2(+) DC) in the spleen, which are both necessary and sufficient for transferring resistance to infection from CpG-treated donors to naive recipients. These CpG-activated Thy1.2(+) DC are distinct from conventional (CD11c(hi), Thy1.2(-)) or plasmacytoid DC (mPDCA(+)), and secrete IFN-gamma that contributes to protection. These findings suggest that a novel Thy1.2(+) DC subset plays a critical role in mediating the immunoprotective activity of CpG DNA.
引用
收藏
页码:2397 / 2405
页数:9
相关论文
共 50 条
  • [1] Dendritic Cells in Listeria monocytogenes Infection
    Edelson, Brian T.
    IMMUNITY TO LISTERIA MONOCYTOGENES, 2012, 113 : 33 - 49
  • [2] Alternative processing for MHC class I presentation by immature and CpG-activated dendritic cells
    Chen, LY
    Jondal, M
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (04) : 952 - 960
  • [3] CYLD-deficiency protects against lethal infection with Listeria monocytogenes
    Krishna, N. Gopala
    Wex, K.
    Massoumi, R.
    Borucki, K.
    Schweitzer, K.
    Naumann, N.
    Schlueter, D.
    IMMUNOLOGY, 2012, 137 : 247 - 247
  • [4] NK dendritic cells are innate immune responders to Listeria monocytogenes infection
    Plitas, George
    Chaudhry, Umer I.
    Kingham, T. Peter
    Raab, Jesse R.
    DeMatteo, Ronald P.
    JOURNAL OF IMMUNOLOGY, 2007, 178 (07): : 4411 - 4416
  • [5] Activated mouse eosinophils protect against lethal respiratory virus infection
    Percopo, Caroline M.
    Dyer, Kimberly D.
    Ochkur, Sergei I.
    Luo, Janice L.
    Fischer, Elizabeth R.
    Lee, James J.
    Lee, Nancy A.
    Domachowske, Joseph B.
    Rosenberg, Helene F.
    BLOOD, 2014, 123 (05) : 743 - 752
  • [6] The protective role of Kupffer cells against a primary infection with Listeria monocytogenes
    Ebe, Y
    Umezu, H
    Hasegawa, G
    Arakawa, M
    Mitsuyama, M
    Naito, M
    CELLS OF THE HEPATIC SINUSOID, VOL 7, 1999, : 230 - 231
  • [7] Natural killer dendritic cells produce IFN-γ in response to Listeria monocytogenes infection
    Plitas, George
    Chaudhry, Umer I.
    Kingham, T. Peter
    Stableford, Jennifer A.
    Raab, Jesse
    DeMatteo, Ronald P.
    JOURNAL OF IMMUNOLOGY, 2006, 176 : S109 - S109
  • [8] Colony-stimulating factor 1-dependent cells protect against systemic infection with Listeria monocytogenes but facilitate neuroinvasion
    Jin, YX
    Dons, L
    Kristensson, K
    Rottenberg, ME
    INFECTION AND IMMUNITY, 2002, 70 (08) : 4682 - 4686
  • [9] Liver-resident CD44hiCD27- γδT Cells Help to Protect Against Listeria monocytogenes Infection
    Wang, Yanan
    Hu, Yuan
    Liu, Yuxia
    Shi, Chongdeng
    Yu, Linyan
    Lu, Nan
    Zhang, Cai
    CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2023, 16 (06): : 923 - 941
  • [10] Cells of myeloid origin are required for type IIFN production and the enhancement of lethal Listeria monocytogenes infection
    Kastner, R.
    Kernbauer, E.
    Stockinger, S.
    Westermayer, S.
    Pilz, A.
    Reutterer, B.
    Kalinke, U.
    Mueller, M.
    Decker, T.
    WIENER KLINISCHE WOCHENSCHRIFT, 2008, 120 : 149 - 150