Cooperative Stimulation of Dendritic Cells by Cryptococcus neoformans Mannoproteins and CpG Oligodeoxynucleotides

被引:49
作者
Dan, Jennifer M. [1 ,2 ]
Wang, Jennifer P. [2 ]
Lee, Chrono K. [2 ]
Levitz, Stuart M. [1 ,2 ]
机构
[1] Boston Univ, Sch Med, Dept Microbiol, Immunol Training Program, Boston, MA 02118 USA
[2] Univ Massachusetts, Med Sch, Dept Med, Div Infect Dis, Worcester, MA USA
来源
PLOS ONE | 2008年 / 3卷 / 04期
基金
美国国家卫生研究院;
关键词
D O I
10.1371/journal.pone.0002046
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While mannosylation targets antigens to mannose receptors on dendritic cells (DC), the resultant immune response is suboptimal. We hypothesized that the addition of toll-like receptor (TLR) ligands would enhance the DC response to mannosylated antigens. Cryptococcus neoformans mannoproteins (MP) synergized with CpG-containing oligodeoxynucleotides to stimulate enhanced production of proinflammatory cytokines and chemokines from murine conventional and plasmacytoid DC. Synergistic stimulation required the interaction of mannose residues on MP with the macrophage mannose receptor (MR), CD206. Moreover, synergy with MP was observed with other TLR ligands, including tripalmitoylated lipopeptide (Pam3CSK4), polyinosine-polycytidylic acid (pI: C), and imiquimod. Finally, CpG enhanced MP-specific MHC II-restricted CD4(+) T-cell responses by a mechanism dependent upon DC expression of CD206 and TLR9. These data suggest a rationale for vaccination strategies that combine mannosylated antigens with TLR ligands and imply that immune responses to naturally mannosylated antigens on pathogens may be greatly augmented if TLR and MR are cooperatively stimulated.
引用
收藏
页数:8
相关论文
共 40 条
[1]   Cryptococcal meningitis [J].
Bicanic, T ;
Harrison, TS .
BRITISH MEDICAL BULLETIN, 2005, 72 (01) :99-118
[2]   On regulation of phagosome maturation and antigen presentation [J].
Blander, J. Magarian ;
Medzhitov, Ruslan .
NATURE IMMUNOLOGY, 2006, 7 (10) :1029-1035
[3]   Toll-dependent selection of microbial antigens for presentation by dendritic cells [J].
Blander, JM ;
Medzhitov, R .
NATURE, 2006, 440 (7085) :808-812
[4]   Dual function of C-type lectin-like receptors in the immune system [J].
Cambi, A ;
Figdor, CG .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (05) :539-546
[5]   Cross-linking of the mannose receptor on monocyte-derived dendritic cells activates an anti-inflammatory immunosuppressive program [J].
Chieppa, M ;
Bianchi, G ;
Doni, A ;
Del Prete, A ;
Sironi, M ;
Laskarin, G ;
Monti, P ;
Piemonti, L ;
Biondi, A ;
Mantovani, A ;
Introna, M ;
Allavena, P .
JOURNAL OF IMMUNOLOGY, 2003, 171 (09) :4552-4560
[6]   Stimulation via Toll-like receptor 9 reduces Cryptococcus neoformans-induced pulmonary inflammation in an IL-12-dependent manner [J].
Edwards, L ;
Williams, AE ;
Krieg, AM ;
Rae, AJ ;
Snelgrove, RJ ;
Hussell, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (01) :273-281
[7]   Collaborative induction of inflammatory responses by dectin-1 and toll-like receptor 2 [J].
Gantner, BN ;
Simmons, RM ;
Canavera, SJ ;
Akira, S ;
Underhill, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (09) :1107-1117
[8]  
Guy B, 2007, NAT REV MICROBIOL, V5, P505, DOI 10.1038/nrmicro1681
[9]   Immune cell activation by bacterial CpG-DNA through myeloid differentiation marker 88 and tumor necrosis factor receptor-associated factor (TRAF)6 [J].
Häcker, H ;
Vabulas, RM ;
Takeuchi, O ;
Hoshino, K ;
Akira, S ;
Wagner, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (04) :595-600
[10]   Role of phosphoinositide 3-kinase in innate immunity [J].
Hazeki, Kaoru ;
Nigorikawa, Kiyomi ;
Hazeki, Osamu .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2007, 30 (09) :1617-1623