Dendritic Cells in Anticancer Vaccination: Rationale for Ex Vivo Loading or In Vivo Targeting

被引:64
作者
Baldin, Alexey V. [1 ]
Savvateeva, Lyudmila V. [1 ]
Bazhin, Alexandr V. [2 ,3 ]
Zamyatnin, Andrey A., Jr. [1 ,4 ]
机构
[1] Sechenov First Moscow State Med Univ, Inst Mol Med, Moscow 119991, Russia
[2] Ludwig Maximilians Univ Munchen, Dept Gen Visceral & Transplant Surg, Munich 81377, Germany
[3] German Canc Consortium DKTK, Partner Site Munich, Munich 80336, Germany
[4] Lomonosov Moscow State Univ, Belozersky Inst Physicochem Biol, Dept Cell Signaling, Moscow 119991, Russia
关键词
cancer immunotherapy; combination immunotherapy; anticancer vaccine; dendritic cells; dendritic cell vaccine; dendritic cell targeting; CD8(+) T-CELL; MHC CLASS-I; HEAT-SHOCK PROTEINS; ANTIGEN CROSS-PRESENTATION; TUMOR-ASSOCIATED ANTIGEN; MANNOSE RECEPTOR; IMMUNE-RESPONSES; PHASE-I; DC-SIGN; GM-CSF;
D O I
10.3390/cancers12030590
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dendritic cells (DCs) have shown great potential as a component or target in the landscape of cancer immunotherapy. Different in vivo and ex vivo strategies of DC vaccine generation with different outcomes have been proposed. Numerous clinical trials have demonstrated their efficacy and safety in cancer patients. However, there is no consensus regarding which DC-based vaccine generation method is preferable. A problem of result comparison between trials in which different DC-loading or-targeting approaches have been applied remains. The employment of different DC generation and maturation methods, antigens and administration routes from trial to trial also limits the objective comparison of DC vaccines. In the present review, we discuss different methods of DC vaccine generation. We conclude that standardized trial designs, treatment settings and outcome assessment criteria will help to determine which DC vaccine generation approach should be applied in certain cancer cases. This will result in a reduction in alternatives in the selection of preferable DC-based vaccine tactics in patient. Moreover, it has become clear that the application of a DC vaccine alone is not sufficient and combination immunotherapy with recent advances, such as immune checkpoint inhibitors, should be employed to achieve a better clinical response and outcome.
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页数:42
相关论文
共 271 条
[1]   Glycan modification of the tumor antigen gp100 targets DC-SIGN to enhance dendritic cell induced antigen presentation to T cells [J].
Aanoudse, Corlien A. ;
Bax, Marieke ;
Sanchez-Hernandez, Marta ;
Garcia-Vallejo, Juan J. ;
van Kooyk, Yvette .
INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (04) :839-846
[2]  
ABRAHAM R, 1995, J IMMUNOL, V154, P1
[3]   Chloroquine enhances human CD8+ T cell responses against soluble antigens in vivo [J].
Accapezzato, D ;
Visco, V ;
Francavilla, V ;
Molette, C ;
Donato, T ;
Paroli, M ;
Mondelli, MU ;
Doria, M ;
Torrisi, MR ;
Barnaba, V .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (06) :817-828
[4]   Phase I Study of the Humanized Anti-CD40 Monoclonal Antibody Dacetuzumab in Refractory or Recurrent Non-Hodgkin's Lymphoma [J].
Advani, Ranjana ;
Forero-Torres, Andres ;
Furman, Richard R. ;
Rosenblatt, Joseph D. ;
Younes, Anas ;
Ren, Hong ;
Harrop, Kate ;
Whiting, Nancy ;
Drachman, Jonathan G. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (26) :4371-4377
[5]   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
[6]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[7]   Clinical use of dendritic cells for cancer therapy [J].
Anguille, Sebastien ;
Smits, Evelien L. ;
Lion, Eva ;
van Tendeloo, Viggo F. ;
Berneman, Zwi N. .
LANCET ONCOLOGY, 2014, 15 (07) :E257-E267
[8]  
Apostolopoulos V., 2001, Current Molecular Medicine (Hilversum), V1, P469, DOI 10.2174/1566524013363645
[9]  
Apostolopoulos V, 2000, EUR J IMMUNOL, V30, P1714, DOI 10.1002/1521-4141(200006)30:6<1714::AID-IMMU1714>3.0.CO
[10]  
2-C