New generation of dendritic cell vaccines

被引:27
作者
Radford, Kristen J. [1 ,2 ]
Caminschi, Irina [3 ,4 ]
机构
[1] Mater Med Res Inst, Canc Immunotherapies Grp, South Brisbane, Qld, Australia
[2] Univ Queensland, Sch Med, Herston, Qld, Australia
[3] Burnet Inst, Ctr Immunol, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
dendritic cells; vaccines; targeting; tumor immunity; cytotoxic T cells; ANTIGEN CROSS-PRESENTATION; CUTTING EDGE; STEADY-STATE; IN-VIVO; T-CELLS; RECEPTOR; MOUSE; IMMUNITY; RESPONSES; EXPRESSION;
D O I
10.4161/hv.22487
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dendritic cells (DC) play a pivotal role in the induction and regulation of immune responses, including the induction of cytotoxic T lymphocytes (CTL) responses. These are essential for the eradication of cancers and pathogens including HIV and malaria, for which there are currently no effective vaccines. New developments in our understanding of DC biology have identified the key DC subset responsible for CTL induction, which is now an attractive candidate to target for vaccination. These DC are characterized by expression of novel markers Clec9A and XCR1, and a specialized capacity to cross-present antigen (Ag) from tumors and pathogens that do not directly infect DC. New generation DC vaccines that specifically target the cross-presenting DC in vivo have already demonstrated potential in preclinical animal models but the challenge remains to translate these findings into clinically efficacous vaccines in man. This has been greatly facilitated by the recent identification of the equivalent Clec9A(+)XCR1(+) cross-presenting DC in human lymphoid tissues and peripheral tissues that are key sites for vaccination administration. These findings combined with further studies on DC subset biology have important implications for the design of new CTL-mediated vaccines.
引用
收藏
页码:259 / 264
页数:6
相关论文
共 72 条
[1]   F-Actin Is an Evolutionarily Conserved Damage-Associated Molecular Pattern Recognized by DNGR-1, a Receptor for Dead Cells [J].
Ahrens, Susan ;
Zelenay, Santiago ;
Sancho, David ;
Hanc, Pavel ;
Kjaer, Svend ;
Feest, Christoph ;
Fletcher, Georgina ;
Durkin, Charlotte ;
Postigo, Antonio ;
Skehel, Mark ;
Batista, Facundo ;
Thompson, Barry ;
Way, Michael ;
Sousa, Caetano Reis e ;
Schulz, Oliver .
IMMUNITY, 2012, 36 (04) :635-645
[2]   Migratory dendritic cells transfer antigen to a lymph node-resident dendritic cell population for efficient CTL priming [J].
Allan, Rhys S. ;
Waithman, Jason ;
Bedoui, Sammy ;
Jones, Claerwen M. ;
Villadangos, Jose A. ;
Zhan, Yifan ;
Lew, Andrew M. ;
Shortman, Ken ;
Heath, William R. ;
Carbone, Francis R. .
IMMUNITY, 2006, 25 (01) :153-162
[3]   Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology [J].
Asselin-Paturel, C ;
Boonstra, A ;
Dalod, M ;
Durand, I ;
Yessaad, N ;
Dezutter-Dambuyant, C ;
Vicari, A ;
O'Garra, A ;
Biron, C ;
Brière, F ;
Trinchieri, G .
NATURE IMMUNOLOGY, 2001, 2 (12) :1144-1150
[4]   Expression of XCR1 characterizes the Batf3-dependent lineage of dendritic cells capable of antigen cross-presentation [J].
Bachem, Annabell ;
Hartung, Evelyn ;
Guettler, Steffen ;
Mora, Ahmed ;
Zhou, Xuefei ;
Hegemann, Anika ;
Plantinga, Maud ;
Mazzini, Elisa ;
Stoitzner, Patrizia ;
Gurka, Stephanie ;
Henn, Volker ;
Mages, Hans W. ;
Kroczek, Richard A. .
FRONTIERS IN IMMUNOLOGY, 2012, 3
[5]   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
[6]   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
[7]   What Role Does the Route of Immunization Play in the Generation of Protective Immunity against Mucosal Pathogens? [J].
Belyakov, Igor M. ;
Ahlers, Jeffrey D. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (11) :6883-6892
[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