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
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