Carbohydrate-mediated targeting of antigen to dendritic cells leads to enhanced presentation of antigen to T cells

被引:64
作者
Adams, Eddie W. [2 ]
Ratner, Daniel M. [2 ,3 ]
Seeberger, Peter H. [2 ,4 ]
Hacohen, Nir [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Immunol & Inflammatory Dis, Charlestown, MA 02129 USA
[2] MIT, Dept Chem, Cambridge, MA 02139 USA
[3] Boston Med Ctr, Infect Dis Sect, Boston, MA 02118 USA
[4] ETH, Organ Chem Lab, CH-8093 Zurich, Switzerland
关键词
carbohydrates; dendritic cells; glycoconjugates; targeting; tolerance;
D O I
10.1002/cbic.200700310
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The unique therapeutic value of dendritic cells (DCs) for the treatment of allergy, autoimmunity and transplant rejection is predicated upon our ability to selectively deliver antigens, drugs or nucleic acids to DCs in vivo. Here we describe a method for delivering whole protein antigens to DCs based on carbohydrate-mediated targeting of DC-expressed lectins. A series of synthetic carbohydrates was chemically-coupled to a model antigen, I ovalbumin (OVA), and each conjugate was evaluated for its ability to increase the efficiency of antigen presentation by murine I DCs to OVA-specific T cells (CD4(+) and CD8(+)). In vitro data ore presented that demonstrate that carbohydrate modification of OVA leads to a 50-fold enhancement of presentation of antigenic peptide to CD4(+) T cells. A tenfold enhancement is observed for CD8(+) T cells; this indicates that the targeted lectin(s) can mediate cross-presentation of antigens on MHC class I. Our data indicate that the observed enhancements in antigen presentation are unique to OVA that is conjugated to complex oligosaccharides, such as a high-mannose nonasaccharide, but not to monosaccharides. Taken together, our data suggest that a DC targeting strategy that is based upon carbohydrate-lectin interactions is a promising approach for enhancing antigen presentation via class I and class II molecules.
引用
收藏
页码:294 / 303
页数:10
相关论文
共 30 条
  • [1] Cutting edge: Carbohydrate profiling identifies new pathogens that interact with dendritic cell-specific ICAM-3-grabbing nonintegrin on dendritic cells
    Appelmelk, BJ
    van Die, I
    van Vliet, SJ
    Vandenbroucke-Grauls, CMJE
    Geijtenbeek, TBH
    van Kooyk, Y
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 170 (04) : 1635 - 1639
  • [2] A schistosome-expressed immunomodulatory glycoconjugate expands peritoneal Gr1+ macrophages that suppress naive CD4+ T cell proliferation via an IFN-γ and nitric oxide-dependent mechanism
    Atochina, O
    Daly-Engel, T
    Piskorska, D
    McGuire, E
    Harn, DA
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 167 (08) : 4293 - 4302
  • [3] Efficient targeting of protein antigen to the dendritic cell receptor DEC-205 in the steady state leads to antigen presentation on major histocompatibility complex class I products and peripheral CD8+ T cell tolerance
    Bonifaz, L
    Bonnyay, D
    Mahnke, K
    Rivera, M
    Nussenzweig, MC
    Steinman, RM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) : 1627 - 1638
  • [4] Functional comparison of mouse CIRE/mouse DC-SIGN and human DC-SIGN
    Caminschi, I
    Corbett, AJ
    Zahra, C
    Lahoud, M
    Lucas, KM
    Sofi, M
    Vremec, D
    Gramberg, T
    Pöhlmann, S
    Curtis, J
    Handman, E
    van Dommelen, SLH
    Fleming, P
    Degli-Esposti, MA
    Shortman, K
    Wright, MD
    [J]. INTERNATIONAL IMMUNOLOGY, 2006, 18 (05) : 741 - 753
  • [5] Molecular cloning of a C-type lectin superfamily protein differentially expressed by CD8α- splenic dendritic cells
    Caminschi, I
    Lucas, KM
    O'Keeffe, MA
    Hochrein, H
    Laâbi, Y
    Brodnicki, TC
    Lew, AM
    Shortman, K
    Wright, MD
    [J]. MOLECULAR IMMUNOLOGY, 2001, 38 (05) : 365 - 373
  • [6] Structural basis for selective recognition of oligosaccharides by DC-SIGN and DC-SIGNR
    Feinberg, H
    Mitchell, DA
    Drickamer, K
    Weis, WI
    [J]. SCIENCE, 2001, 294 (5549) : 2163 - 2166
  • [7] C-type lectin receptors on dendritic cells and Langerhans cells
    Figdor, CG
    van Kooyk, Y
    Adema, GJ
    [J]. NATURE REVIEWS IMMUNOLOGY, 2002, 2 (02) : 77 - 84
  • [8] High and low affinity carbohydrate ligands revealed for murine SIGN-R1 by carbohydrate array and cell binding approaches, and differing specificities for SIGN-R3 and langerin
    Galustian, C
    Park, CG
    Chai, WG
    Kiso, M
    Bruening, SA
    Kang, YS
    Steinman, RM
    Feizi, T
    [J]. INTERNATIONAL IMMUNOLOGY, 2004, 16 (06) : 853 - 866
  • [9] Marginal zone macrophages express a murine homologue of DC-SIGN that captures blood-borne antigens in vivo
    Geijtenbeek, TBH
    Groot, PC
    Nolte, MA
    van Vliet, SJ
    Gangaram-Panday, ST
    van Duijnhoven, GCF
    Kraal, G
    van Oosterhout, AJM
    van Kooyk, Y
    [J]. BLOOD, 2002, 100 (08) : 2908 - 2916
  • [10] Mycobacteria target DC-SIGN to suppress dendritic cell function
    Geijtenbeek, TBH
    van Vliet, SJ
    Koppel, EA
    Sanchez-Hernandez, M
    Vandenbroucke-Grauls, CMJE
    Appelmelk, B
    van Kooyk, Y
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (01) : 7 - 17