Peptide-Conjugated PAMAM Dendrimer as a Universal DNA Vaccine Platform to Target Antigen-Presenting Cells

被引:85
|
作者
Daftarian, Pirouz [2 ]
Kaifer, Angel E. [5 ,6 ]
Li, Wei [5 ,6 ]
Blomberg, Bonnie B.
Frasca, Daniela
Roth, Felix
Chowdhury, Raquibul
Berg, Eric A. [8 ]
Fishman, Jordan B. [8 ]
Al Sayegh, Husain A. [7 ]
Blackwelder, Pat [7 ]
Inverardi, Luca [3 ]
Perez, Victor L. [2 ]
Lemmon, Vance [4 ]
Serafini, Paolo [1 ,3 ]
机构
[1] Univ Miami, Dept Microbiol & Immunol, Sylvester Canc Ctr, Miller Sch Med, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Bascom Palmer Eye Inst, Miami, FL 33136 USA
[3] Univ Miami, Miller Sch Med, Diabet Res Inst, Miami, FL 33136 USA
[4] Univ Miami, Miller Sch Med, Dept Neurol Surg, Miami Project Cure Paralysis, Miami, FL 33136 USA
[5] Univ Miami, Ctr Supramol Sci, Coral Gables, FL 33124 USA
[6] Univ Miami, Dept Chem, Coral Gables, FL 33124 USA
[7] Univ Miami, UMCAM, Coral Gables, FL 33124 USA
[8] 21st Century Biochem Inc, Marlborough, MA USA
关键词
TYROSINASE-RELATED PROTEIN-2; CYTOTOXIC T-LYMPHOCYTES; TUMOR REJECTION; GENETIC VACCINATION; IMMUNE-RESPONSES; B16; MELANOMA; IN-VIVO; ELECTROPORATION; DELIVERY; IMMUNOGENICITY;
D O I
10.1158/0008-5472.CAN-11-1766
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA-based vaccines hold promise to outperform conventional antigen-based vaccines by virtue of many unique features. However, DNA vaccines have thus far fallen short of expectations, due in part to poor targeting of professional antigen-presenting cells (APC) and low immunogenicity. In this study, we describe a new platform for effective and selective delivery of DNA to APCs in vivo that offers intrinsic immune-enhancing characteristics. This platform is based on conjugation of fifth generation polyamidoamine (G5-PAMAM) dendrimers, a DNA-loading surface, with MHC class II-targeting peptides that can selectively deliver these dendrimers to APCs under conditions that enhance their immune stimulatory potency. DNA conjugated with this platform efficiently transfected murine and human APCs in vitro. Subcutaneous administration of DNA-peptide-dendrimer complexes in vivo preferentially transfected dendritic cells (DC) in the draining lymph nodes, promoted generation of high affinity T cells, and elicited rejection of established tumors. Taken together, our findings show how PAMAM dendrimer complexes can be used for high transfection efficiency and effective targeting of APCs in vivo, conferring properties essential to generate effective DNA vaccines. Cancer Res; 71(24); 7452-62. (C) 2011 AACR.
引用
收藏
页码:7452 / 7462
页数:11
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