Targeted antigen delivery and activation of dendritic cells in vivo: Steps towards cost effective vaccines

被引:117
作者
Tacken, Paul J. [1 ]
Figdor, Carl G. [1 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Tumor Immunol, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
关键词
Dendritic cell; Vaccine; Adjuvant; Targeting; Cancer; Immunity; POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID; EPIDERMAL LANGERHANS CELLS; HIV GAG PROTEIN; DC-SIGN; CROSS-PRESENTATION; T-CELLS; PRESENTING CELLS; MANNOSE RECEPTOR; DISTINCT POPULATIONS; TUMOR-IMMUNOTHERAPY;
D O I
10.1016/j.smim.2011.01.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
During the past decade, the immunotherapeutic potential of ex vivo generated professional antigen presenting dendritic cells (DCs) has been explored in the clinic. Albeit safe, clinical results have thus far been limited. A major disadvantage of current cell-based dendritic cell (DC) therapies, preventing universal implementation of this form of immunotherapy, is the requirement that vaccines need to be tailor made for each individual. Targeted delivery of antigens to DC surface receptors in vivo would circumvent this laborious and expensive ex vivo culturing steps involved with these cell-based therapies. In addition, the opportunity to target natural and often rare DC subsets in vivo might have advantages over loading more artificial ex vivo cultured DCs. Preclinical studies show targeting antigens to DCs effectively induces humoral responses, while cellular responses are induced provided a DC maturation or activation stimulus is co-administered. Here, we discuss strategies to target antigens to distinct DC subsets and to simultaneously employ adjuvants to activate these cells to induce immunity. (C) 2011 Published by Elsevier Ltd.
引用
收藏
页码:12 / 20
页数:9
相关论文
共 125 条
[1]
CD14+ antigen-presenting cells in human dermis are less mature than their CD1a+ counterparts [J].
Angel, Catherine E. ;
Lala, Aisha ;
Chen, Chun-Jen J. ;
Edgar, Stephen G. ;
Ostrovsky, Lena L. ;
Dunbar, P. Rod .
INTERNATIONAL IMMUNOLOGY, 2007, 19 (11) :1271-1279
[2]
Distinctive localization of antigen-presenting cells in human lymph nodes [J].
Angel, Catherine E. ;
Chen, Chun-Jen J. ;
Horlacher, Oliver C. ;
Winkler, Sintia ;
John, Thomas ;
Browning, Judy ;
MacGregor, Duncan ;
Cebon, Jonathan ;
Dunbar, P. Rod .
BLOOD, 2009, 113 (06) :1257-1267
[3]
Superior antigen cross-presentation and XCR1 expression define human CD11c+CD141+ cells as homologues of mouse CD8+ dendritic cells [J].
Bachem, Annabell ;
Guettler, Steffen ;
Hartung, Evelyn ;
Ebstein, Frederic ;
Schaefer, Michael ;
Tannert, Astrid ;
Salama, Abdulgabar ;
Movassaghi, Kamran ;
Opitz, Corinna ;
Mages, Hans W. ;
Henn, Volker ;
Kloetzel, Peter-Michael ;
Gurka, Stephanie ;
Kroczek, Richard A. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (06) :1273-1281
[4]
Cross-presentation of viral and self antigens by skin-derived CD103+ dendritic cells [J].
Bedoui, Sammy ;
Whitney, Paul G. ;
Waithman, Jason ;
Eidsmo, Liv ;
Wakim, Linda ;
Caminschi, Irina ;
Allan, Rhys S. ;
Wojtasiak, Magdalena ;
Shortman, Ken ;
Carbone, Francis R. ;
Brooks, Andrew G. ;
Heath, William R. .
NATURE IMMUNOLOGY, 2009, 10 (05) :488-495
[5]
The CD8α+ dendritic cell is responsible for inducing peripheral self-tolerance to tissue-associated antigens [J].
Belz, GT ;
Behrens, GMN ;
Smith, CM ;
Miller, JFAP ;
Jones, C ;
Lejon, K ;
Fathman, CG ;
Mueller, SN ;
Shortman, K ;
Carbone, FR ;
Heath, WR .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (08) :1099-1104
[6]
Plasmacytoid dendritic cells of melanoma patients present exogenous proteins to CD4+ T cells after FcγRII-mediated uptake [J].
Benitez-Ribas, Daniel ;
Adema, Gosse J. ;
Winkels, Gregor ;
Klasen, Ina S. ;
Punt, Cornelis J. A. ;
Figdor, Carl G. ;
de Vries, I. Jolanda M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (07) :1629-1635
[7]
BIRKHOLZ K, 2010, BLOOD
[8]
Toll-dependent selection of microbial antigens for presentation by dendritic cells [J].
Blander, JM ;
Medzhitov, R .
NATURE, 2006, 440 (7085) :808-812
[9]
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 [J].
Bonifaz, L ;
Bonnyay, D ;
Mahnke, K ;
Rivera, M ;
Nussenzweig, MC ;
Steinman, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) :1627-1638
[10]
In vivo targeting of antigens to maturing dendritic cells via the DEC-205 receptor improves T cell vaccination [J].
Bonifaz, LC ;
Bonnyay, DP ;
Charalambous, A ;
Darguste, DI ;
Fujii, SI ;
Soares, H ;
Brimnes, MK ;
Moltedo, B ;
Moran, TM ;
Steinman, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (06) :815-824