Introduction of zwitterionic motifs into bacterial polysaccharides generates TLR2 agonists able to activate APCs

被引:40
作者
Gallorini, Simona [1 ]
Berti, Francesco [1 ]
Parente, Pierino [1 ]
Baronio, Roberta [1 ]
Aprea, Susanna [1 ]
D'Oro, Ugo [1 ]
Pizza, Mariagrazia [1 ]
Telford, John L. [1 ]
Wack, Andreas [1 ]
机构
[1] Novartis Vaccines Res Ctr, Dept Mol Immunol, I-53100 Siena, Italy
关键词
D O I
10.4049/jimmunol.179.12.8208
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It was shown previously that bacterial polysaccharides (PS), which naturally contain both positive and negative charges, are able to activate T cells and APCs. However, the vast majority of bacterial PS are anionic and do not have these properties. In this study, we show that chemical introduction of positive charges into naturally anionic bacterial PS confers to the resulting zwitterionic PS (ZPS) the ability to activate pure human monocytes, monocyte-derived dendritic cells, and mouse bone marrow-derived dendritic cells, as do natural bacterial ZPS. Cells are induced to up-regulate MHC class II and costimulatory molecules and to produce cytokines. In mixed monocyte-T cell cocultures, ZPS induce MHC II-dependent T cell proliferation and up-regulation of activation markers. These stimulatory qualities of ZPS disappear when the positive charge is chemically removed from the molecules and thus the zwitterionic motif is destroyed. The ability of natural and chemically derived ZPS to activate APCs can be blocked by anti-TLR2 mAbs, and TLR2 transfectants show reporter gene transcription upon incubation with ZPS. In conclusion, the generation of a zwitterionic motif in bacterial PS confers the ability to activate both APCs and T cells. This finding has important implications for the design of novel polysaccharide vaccines.
引用
收藏
页码:8208 / 8215
页数:8
相关论文
共 28 条
[1]  
Brubaker JO, 1999, J IMMUNOL, V162, P2235
[2]   CD4+T cells mediate abscess formation in intra-abdominal sepsis by an IL-17-dependent mechanism [J].
Chung, DR ;
Kasper, DL ;
Panzo, RJ ;
Chtinis, T ;
Grusby, MJ ;
Sayegh, MH ;
Tzianabos, AO .
JOURNAL OF IMMUNOLOGY, 2003, 170 (04) :1958-1963
[3]   Polysaccharide processing and presentation by the MHCII pathway [J].
Cobb, BA ;
Wang, O ;
Tzianabos, AO ;
Kasper, DL .
CELL, 2004, 117 (05) :677-687
[4]   DEVELOPMENT AND PHASE-1 CLINICAL-TESTING OF A CONJUGATE VACCINE AGAINST MENINGOCOCCUS-A AND MENINGOCOCCUS-C [J].
COSTANTINO, P ;
VITI, S ;
PODDA, A ;
VELMONTE, MA ;
NENCIONI, L ;
RAPPUOLI, R .
VACCINE, 1992, 10 (10) :691-698
[5]   TLR2 engagement on CD8 T cells lowers the threshold for optimal antigen-induced T cell activation [J].
Cottalorda, Anne ;
Verschelde, Claire ;
Marcais, Antoine ;
Tomkowiak, Martine ;
Musette, Philippe ;
Uematsu, Satoshi ;
Akira, Shizuo ;
Marvel, Jacqueline ;
Bonnefoy-Berard, Nathalie .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2006, 36 (07) :1684-1693
[6]   A totally synthetic vaccine of generic structure that targets Toll-like receptor 2 on dendritic cells and promotes antibody or cytotoxic T cell responses [J].
Jackson, DC ;
Lau, YF ;
Le, T ;
Suhrbier, A ;
Deliyannis, G ;
Cheers, C ;
Smith, C ;
Zeng, WG ;
Brown, LE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (43) :15440-15445
[7]   Effect of molecular size on the ability of zwitterionic polysaccharides to stimulate cellular immunity [J].
Kalka-Moll, WM ;
Tzianabos, AO ;
Wang, Y ;
Carey, VJ ;
Finberg, RW ;
Onderdonk, AB ;
Kasper, DL .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :719-724
[8]   Zwitterionic polysaccharides stimulate T cells by MHC class II-dependent interactions [J].
Kalka-Moll, WM ;
Tzianabos, AO ;
Bryant, PW ;
Niemeyer, M ;
Ploegh, HL ;
Kasper, DL .
JOURNAL OF IMMUNOLOGY, 2002, 169 (11) :6149-6153
[9]   TLR2 is expressed on activated T cells as a costimulatory receptor [J].
Komai-Koma, M ;
Jones, L ;
Ogg, GS ;
Xu, DM ;
Liew, FY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :3029-3034
[10]   Toll-like receptor 2 signaling modulates the functions of CD4+CD25+ regulatory T cells [J].
Liu, HY ;
Komai-Koma, M ;
Xu, D ;
Liew, FY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (18) :7048-7053