Acknowledgement
Supported by : National Research Foundation of KOREA (NRF)
References
- Steinman RM, Cohn ZA. Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution. J Exp Med 1973;137:1142-62. https://doi.org/10.1084/jem.137.5.1142
- Steinman RM, Nussenzweig MC. Dendritic cells: features and functions. Immunol Rev 1980;53:127-47. https://doi.org/10.1111/j.1600-065X.1980.tb01042.x
- Banchereau J, Steinman RM. Dendritic cells and the control of immunity. Nature 1998;392:245-52. https://doi.org/10.1038/32588
- Banchereau J, Briere F, Caux C, et al. Immunobiology of dendritic cells. Annu Rev Immunol 2000;18:767-811. https://doi.org/10.1146/annurev.immunol.18.1.767
- Mellman I, Steinman RM. Dendritic cells: specialized and regulated antigen processing machines. Cell 2001;106:255-8. https://doi.org/10.1016/S0092-8674(01)00449-4
- Steinman RM. The dendritic cell system and its role in immunogenicity. Annu Rev Immunol 1991;9:271-96. https://doi.org/10.1146/annurev.iy.09.040191.001415
- Munz C, Steinman RM, Fujii S. Dendritic cell maturation by innate lymphocytes: coordinated stimulation of innate and adaptive immunity. J Exp Med 2005;202:203-7. https://doi.org/10.1084/jem.20050810
- Steinman RM. Decisions about dendritic cells: past, present, and future. Annu Rev Immunol 2012;30:1-22. https://doi.org/10.1146/annurev-immunol-100311-102839
- Steinman RM, Pack M, Inaba K. Dendritic cell development and maturation. Adv Exp Med Biol 1997;417:1-6.
- Steinman RM, Idoyaga J. Features of the dendritic cell lineage. Immunol Rev 2010;234:5-17. https://doi.org/10.1111/j.0105-2896.2009.00888.x
- Steinman RM, Inaba K, Turley S, Pierre P, Mellman I. Antigen capture, processing, and presentation by dendritic cells: recent cell biological studies. Hum Immunol 1999;60:562-7. https://doi.org/10.1016/S0198-8859(99)00030-0
- Cella M, Engering A, Pinet V, Pieters J, Lanzavecchia A. Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells. Nature 1997;388:782-7. https://doi.org/10.1038/42030
- Guermonprez P, Valladeau J, Zitvogel L, Thery C, Amigorena S. Antigen presentation and T cell stimulation by dendritic cells. Annu Rev Immunol 2002;20:621-67. https://doi.org/10.1146/annurev.immunol.20.100301.064828
- Alvarez D, Vollmann EH, von Andrian UH. Mechanisms and consequences of dendritic cell migration. Immunity 2008;29:325-42. https://doi.org/10.1016/j.immuni.2008.08.006
- Thery C, Amigorena S. The cell biology of antigen presentation in dendritic cells. Curr Opin Immunol 2001;13:45-51. https://doi.org/10.1016/S0952-7915(00)00180-1
- Bonasio R, von Andrian UH. Generation, migration and function of circulating dendritic cells. Curr Opin Immunol 2006;18:503-11. https://doi.org/10.1016/j.coi.2006.05.011
- MartIn-Fontecha A, Sebastiani S, Hopken UE, et al. Regulation of dendritic cell migration to the draining lymph node: impact on T lymphocyte traffic and priming. J Exp Med 2003;198:615-21. https://doi.org/10.1084/jem.20030448
- Dieu MC, Vanbervliet B, Vicari A, et al. Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites. J Exp Med 1998;188:373-86. https://doi.org/10.1084/jem.188.2.373
- Randolph GJ, Sanchez-Schmitz G, Angeli V. Factors and signals that govern the migration of dendritic cells via lymphatics: recent advances. Springer Semin Immunopathol 2005;26:273-87. https://doi.org/10.1007/s00281-004-0168-0
- Cavanagh LL, Bonasio R, Mazo IB, et al. Activation of bone marrow-resident memory T cells by circulating, antigenbearing dendritic cells. Nat Immunol 2005;6:1029-37. https://doi.org/10.1038/ni1249
- Shortman K, Liu YJ. Mouse and human dendritic cell subtypes. Nat Rev Immunol 2002;2:151-61. https://doi.org/10.1038/nri746
- Shortman K, Naik SH. Steady-state and inflammatory dendritic-cell development. Nat Rev Immunol 2007;7:19-30. https://doi.org/10.1038/nri1996
- MacDonald KP, Munster DJ, Clark GJ, Dzionek A, Schmitz J, Hart DN. Characterization of human blood dendritic cell subsets. Blood 2002;100:4512-20. https://doi.org/10.1182/blood-2001-11-0097
- Dzionek A, Fuchs A, Schmidt P, et al. BDCA-2, BDCA-3, and BDCA-4: three markers for distinct subsets of dendritic cells in human peripheral blood. J Immunol 2000;165: 6037-46. https://doi.org/10.4049/jimmunol.165.11.6037
- Shortman K, Heath WR. The CD8+ dendritic cell subset. Immunol Rev 2010;234:18-31. https://doi.org/10.1111/j.0105-2896.2009.00870.x
- Villadangos JA, Schnorrer P. Intrinsic and cooperative antigen-presenting functions of dendritic-cell subsets in vivo. Nat Rev Immunol 2007;7:543-55. https://doi.org/10.1038/nri2103
- den Haan JM, Lehar SM, Bevan MJ. CD8(+) but not CD8(-) dendritic cells cross-prime cytotoxic T cells in vivo. J Exp Med 2000;192:1685-96. https://doi.org/10.1084/jem.192.12.1685
- Hochrein H, Shortman K, Vremec D, Scott B, Hertzog P, O'Keeffe M. Differential production of IL-12, IFN-alpha, and IFN-gamma by mouse dendritic cell subsets. J Immunol 2001;166:5448-55. https://doi.org/10.4049/jimmunol.166.9.5448
- Vremec D, Pooley J, Hochrein H, Wu L, Shortman K. CD4 and CD8 expression by dendritic cell subtypes in mouse thymus and spleen. J Immunol 2000;164:2978-86. https://doi.org/10.4049/jimmunol.164.6.2978
- del Rio ML, Bernhardt G, Rodriguez-Barbosa JI, Forster R. Development and functional specialization of CD103+ dendritic cells. Immunol Rev 2010;234:268-81. https://doi.org/10.1111/j.0105-2896.2009.00874.x
- Bedoui S, Whitney PG, Waithman J, et al. Cross-presentation of viral and self antigens by skin-derived CD103+ dendritic cells. Nat Immunol 2009;10:488-95. https://doi.org/10.1038/ni.1724
- Liu YJ. IPC: professional type 1 interferon-producing cells and plasmacytoid dendritic cell precursors. Annu Rev Immunol 2005;23:275-306. https://doi.org/10.1146/annurev.immunol.23.021704.115633
- Gilliet M, Cao W, Liu YJ. Plasmacytoid dendritic cells: sensing nucleic acids in viral infection and autoimmune diseases. Nat Rev Immunol 2008;8:594-606. https://doi.org/10.1038/nri2358
- Villadangos JA, Young L. Antigen-presentation properties of plasmacytoid dendritic cells. Immunity 2008;29:352-61. https://doi.org/10.1016/j.immuni.2008.09.002
- Swiecki M, Colonna M. Unraveling the functions of plasmacytoid dendritic cells during viral infections, autoimmunity, and tolerance. Immunol Rev 2010;234:142-62. https://doi.org/10.1111/j.0105-2896.2009.00881.x
- O'Keeffe M, Hochrein H, Vremec D, et al. Mouse plasmacytoid cells: long-lived cells, heterogeneous in surface phenotype and function, that differentiate into CD8(+) dendritic cells only after microbial stimulus. J Exp Med 2002; 196:1307-19. https://doi.org/10.1084/jem.20021031
- Liu K, Waskow C, Liu X, Yao K, Hoh J, Nussenzweig M. Origin of dendritic cells in peripheral lymphoid organs of mice. Nat Immunol 2007;8:578-83. https://doi.org/10.1038/ni1462
- Naik SH, Sathe P, Park HY, et al. Development of plasmacytoid and conventional dendritic cell subtypes from single precursor cells derived in vitro and in vivo. Nat Immunol 2007;8:1217-26. https://doi.org/10.1038/ni1522
- Blasius AL, Giurisato E, Cella M, Schreiber RD, Shaw AS, Colonna M. Bone marrow stromal cell antigen 2 is a specific marker of type I IFN-producing cells in the naive mouse, but a promiscuous cell surface antigen following IFN stimulation. J Immunol 2006;177:3260-5. https://doi.org/10.4049/jimmunol.177.5.3260
- Blasius A, Vermi W, Krug A, Facchetti F, Cella M, Colonna M. A cell-surface molecule selectively expressed on murine natural interferon-producing cells that blocks secretion of interferon-alpha. Blood 2004;103:4201-6. https://doi.org/10.1182/blood-2003-09-3108
- Honda K, Ohba Y, Yanai H, et al. Spatiotemporal regulation of MyD88-IRF-7 signalling for robust type-I interferon induction. Nature 2005;434:1035-40. https://doi.org/10.1038/nature03547
- Sasai M, Linehan MM, Iwasaki A. Bifurcation of Toll-like receptor 9 signaling by adaptor protein 3. Science 2010; 329:1530-4. https://doi.org/10.1126/science.1187029
- Leon B, Lopez-Bravo M, Ardavin C. Monocyte-derived dendritic cells formed at the infection site control the induction of protective T helper 1 responses against Leishmania. Immunity 2007;26:519-31. https://doi.org/10.1016/j.immuni.2007.01.017
- Rotta G, Edwards EW, Sangaletti S, et al. Lipopolysaccharide or whole bacteria block the conversion of inflammatory monocytes into dendritic cells in vivo. J Exp Med 2003; 198:1253-63. https://doi.org/10.1084/jem.20030335
- Ginhoux F, Tacke F, Angeli V, et al. Langerhans cells arise from monocytes in vivo. Nat Immunol 2006;7:265-73.
- Trombetta ES, Mellman I. Cell biology of antigen processing in vitro and in vivo. Annu Rev Immunol 2005;23:975-1028. https://doi.org/10.1146/annurev.immunol.22.012703.104538
- Watts C. Capture and processing of exogenous antigens for presentation on MHC molecules. Annu Rev Immunol 1997;15:821-50. https://doi.org/10.1146/annurev.immunol.15.1.821
- Watts C, Amigorena S. Antigen traffic pathways in dendritic cells. Traffic 2000;1:312-7. https://doi.org/10.1034/j.1600-0854.2000.010404.x
- Sallusto F, Cella M, Danieli C, Lanzavecchia A. Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products. J Exp Med 1995;182:389-400. https://doi.org/10.1084/jem.182.2.389
- Garrett WS, Chen LM, Kroschewski R, et al. Developmental control of endocytosis in dendritic cells by Cdc42. Cell 2000;102:325-34. https://doi.org/10.1016/S0092-8674(00)00038-6
- Palm NW, Medzhitov R. Pattern recognition receptors and control of adaptive immunity. Immunol Rev 2009;227:221-33. https://doi.org/10.1111/j.1600-065X.2008.00731.x
- Amigorena S, Bonnerot C. Fc receptor signaling and trafficking: a connection for antigen processing. Immunol Rev 1999;172:279-84. https://doi.org/10.1111/j.1600-065X.1999.tb01372.x
- East L, Isacke CM. The mannose receptor family. Biochim Biophys Acta 2002;1572:364-86. https://doi.org/10.1016/S0304-4165(02)00319-7
- Weis WI, Taylor ME, Drickamer K. The C-type lectin superfamily in the immune system. Immunol Rev 1998;163:19-34. https://doi.org/10.1111/j.1600-065X.1998.tb01185.x
- Geijtenbeek TB, van Vliet SJ, Engering A, t Hart BA, van Kooyk Y. Self- and nonself-recognition by C-type lectins on dendritic cells. Annu Rev Immunol 2004;22:33-54. https://doi.org/10.1146/annurev.immunol.22.012703.104558
- Mahnke K, Guo M, Lee S, et al. The dendritic cell receptor for endocytosis, DEC-205, can recycle and enhance antigen presentation via major histocompatibility complex class II-positive lysosomal compartments. J Cell Biol 2000;151:673-84. https://doi.org/10.1083/jcb.151.3.673
- Castellino F, Germain RN. Extensive trafficking of MHC class II-invariant chain complexes in the endocytic pathway and appearance of peptide-loaded class II in multiple compartments. Immunity 1995;2:73-88. https://doi.org/10.1016/1074-7613(95)90080-2
- Turley SJ, Inaba K, Garrett WS, et al. Transport of peptide-MHC class II complexes in developing dendritic cells. Science 2000;288:522-7. https://doi.org/10.1126/science.288.5465.522
- Pamer E, Cresswell P. Mechanisms of MHC class I--restricted antigen processing. Annu Rev Immunol 1998;16:323-58. https://doi.org/10.1146/annurev.immunol.16.1.323
- Heath WR, Carbone FR. Cross-presentation, dendritic cells, tolerance and immunity. Annu Rev Immunol 2001;19:47-64. https://doi.org/10.1146/annurev.immunol.19.1.47
- Heath WR, Belz GT, Behrens GM, et al. Cross-presentation, dendritic cell subsets, and the generation of immunity to cellular antigens. Immunol Rev 2004;199:9-26. https://doi.org/10.1111/j.0105-2896.2004.00142.x
- Monu N, Trombetta ES. Cross-talk between the endocytic pathway and the endoplasmic reticulum in cross-presentation by MHC class I molecules. Curr Opin Immunol 2007; 19:66-72. https://doi.org/10.1016/j.coi.2006.11.017
- Joffre OP, Segura E, Savina A, Amigorena S. Cross-presentation by dendritic cells. Nat Rev Immunol 2012;12:557-69. https://doi.org/10.1038/nri3254
- Inaba K, Turley S, Iyoda T, et al. The formation of immunogenic major histocompatibility complex class II-peptide ligands in lysosomal compartments of dendritic cells is regulated by inflammatory stimuli. J Exp Med 2000;191:927-36. https://doi.org/10.1084/jem.191.6.927
- Lanzavecchia A, Sallusto F. Dynamics of T lymphocyte responses: intermediates, effectors, and memory cells. Science 2000;290:92-7. https://doi.org/10.1126/science.290.5489.92
- Bergtold A, Desai DD, Gavhane A, Clynes R. Cell surface recycling of internalized antigen permits dendritic cell priming of B cells. Immunity 2005;23:503-14. https://doi.org/10.1016/j.immuni.2005.09.013
- Kitamura H, Iwakabe K, Yahata T, et al. The natural killer T (NKT) cell ligand alpha-galactosylceramide demonstrates its immunopotentiating effect by inducing interleukin (IL)-12 production by dendritic cells and IL-12 receptor expression on NKT cells. J Exp Med 1999;189:1121-8. https://doi.org/10.1084/jem.189.7.1121
- Sakaguchi S, Yamaguchi T, Nomura T, Ono M. Regulatory T cells and immune tolerance. Cell 2008;133:775-87. https://doi.org/10.1016/j.cell.2008.05.009
- Wing K, Sakaguchi S. Regulatory T cells exert checks and balances on self tolerance and autoimmunity. Nat Immunol 2010;11:7-13.
- Brocker T. The role of dendritic cells in T cell selection and survival. J Leukoc Biol 1999;66:331-5. https://doi.org/10.1002/jlb.66.2.331
- Thompson AG, Thomas R. Induction of immune tolerance by dendritic cells: implications for preventative and therapeutic immunotherapy of autoimmune disease. Immunol Cell Biol 2002;80:509-19. https://doi.org/10.1046/j.1440-1711.2002.01114.x
- Chen M, Wang YH, Wang Y, et al. Dendritic cell apoptosis in the maintenance of immune tolerance. Science 2006; 311:1160-4. https://doi.org/10.1126/science.1122545
- Palucka K, Banchereau J. Dendritic-cell-based therapeutic cancer vaccines. Immunity 2013;39:38-48. https://doi.org/10.1016/j.immuni.2013.07.004
- Mullard A. New cancer vaccines show clinical promise. Nat Rev Drug Discov 2017;16:519.
- Palucka K, Banchereau J. Human dendritic cell subsets in vaccination. Curr Opin Immunol 2013;25:396-402. https://doi.org/10.1016/j.coi.2013.05.001
- Baek S, Lee SJ, Kim MJ, Lee H. Dendritic cell (DC) vaccine in mouse lung cancer minimal residual model: comparison of monocyte-derived DC vs. hematopoietic stem cell derived-DC. Immune Netw 2012;12:269-76. https://doi.org/10.4110/in.2012.12.6.269
- Palucka K, Banchereau J. Cancer immunotherapy via dendritic cells. Nat Rev Cancer 2012;12:265-77. https://doi.org/10.1038/nrc3258
- Carreno BM, Magrini V, Becker-Hapak M, et al. Cancer immunotherapy: a dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells. Science 2015;348:803-8. https://doi.org/10.1126/science.aaa3828
- Palucka K, Ueno H, Fay J, Banchereau J. Harnessing dendritic cells to generate cancer vaccines. Ann N Y Acad Sci 2009;1174:88-98. https://doi.org/10.1111/j.1749-6632.2009.05000.x
- Tacken PJ, Torensma R, Figdor CG. Targeting antigens to dendritic cells in vivo. Immunobiology 2006;211:599-608. https://doi.org/10.1016/j.imbio.2006.05.021
- Thomann JS, Heurtault B, Weidner S, et al. Antitumor activity of liposomal ErbB2/HER2 epitope peptide-based vaccine constructs incorporating TLR agonists and mannose receptor targeting. Biomaterials 2011;32:4574-83. https://doi.org/10.1016/j.biomaterials.2011.03.015
- Gregory AE, Titball R, Williamson D. Vaccine delivery using nanoparticles. Front Cell Infect Microbiol 2013;3:13.
- Chinnasamy N, Treisman JS, Oaks MK, Hanson JP, Chinnasamy D. Ex vivo generation of genetically modified dendritic cells for immunotherapy: implications of lymphocyte contamination. Gene Ther 2005;12:259-71. https://doi.org/10.1038/sj.gt.3302407
- Banchereau J, Palucka AK, Dhodapkar M, et al. Immune and clinical responses in patients with metastatic melanoma to CD34(+) progenitor-derived dendritic cell vaccine. Cancer Res 2001;61:6451-8.
- Gabrilovich DI, Ostrand-Rosenberg S, Bronte V. Coordinated regulation of myeloid cells by tumours. Nat Rev Immunol 2012;12:253-68. https://doi.org/10.1038/nri3175
- De Monte L, Reni M, Tassi E, et al. Intratumor T helper type 2 cell infiltrate correlates with cancer-associated fibroblast thymic stromal lymphopoietin production and reduced survival in pancreatic cancer. J Exp Med 2011;208:469-78. https://doi.org/10.1084/jem.20101876
- Palucka K, Banchereau J, Mellman I. Designing vaccines based on biology of human dendritic cell subsets. Immunity 2010;33:464-78. https://doi.org/10.1016/j.immuni.2010.10.007
- Bonaccorsi I, Pezzino G, Morandi B, Ferlazzo G. Novel perspectives on dendritic cell-based immunotherapy of cancer. Immunol Lett 2013;155:6-10. https://doi.org/10.1016/j.imlet.2013.09.021
- Cavallo F, Offringa R, van der Burg SH, Forni G, Melief CJ. Vaccination for treatment and prevention of cancer in animal models. Adv Immunol 2006;90:175-213.
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