References
1. Kuznetsova M., Lopatnikova J., Shevchenko J., Silkov A., Maksyutov A., Sennikov S. cytotoxic activity and memory t cell subset distribution of in vitro-stimulated CD8+ T cells specific for HER2/neu epitopes. Front. Immunol. 2019; 10: 1017. DOI: 10.3389/fimmu.2019.01017.
2. Kulikova E., Kurilin V., Shevchenko J., Obleukhova I., Khrapov E., Boyarskikh U., et al. Dendritic cells transfected with a DNA construct encoding tumour-associated antigen epitopes induce a cytotoxic immune response against autologous tumour cells in a culture of mononuclear cells from colorectal cancer patients. Scand. J. Immunol. 2015; 82 (2): 110–7. DOI: 10.1111/sji.12311.
3. Mansilla M., Sellès-Moreno C., Fàbregas-Puig S., Amoedo J., Navarro-Barriuso J., Teniente-Serra A., et al. Beneficial effect of tolerogenic dendritic cells pulsed with MOG autoantigen in experimental autoimmune encephalomyelitis. CNS Neurosci. Ther. 2015; 21 (3): 222–30. DOI: 10.1111/cns.12342.
4. Ning B., Wei J., Zhang A., Gong W., Fu J., Jia T., et al. Antigen-specific tolerogenic dendritic cells ameliorate the severity of murine collagen-induced arthritis. PLoS One. 2015; 10 (6): e0131152. DOI: 10.1371/journal.pone.0131152.
5. Sennikov S., Obleukhova I. Methods of induction of tolerant dendritic cells in animals and humans. Immunologiya. 2016; 37 (5): 291–6. DOI: 10.18821/0206-4952-2016-37-5-291-296. (in Russian)
6. Lutz M., Suri R., Niimi M., Ogilvie A., Kukutsch N., Rößner S., et al. Immature dendritic cells generated with low doses of GM-CSF in the absence of IL-4 are maturation resistant and prolong allograft survivalin vivo. Eur. J. Immunol. 2000; 30 (7): 1813–22. DOI: 10.1002/1521-4141(200007)30:7<1813::aid-immu1813>3.0.co;2-8.
7. Fujita S., Sato Y., Sato K., Eizumi K., Fukaya T., Kubo M., et al. Regulatory dendritic cells protect against cutaneous chronic graft-versus-host disease mediated through CD4+CD25+Foxp3+ regulatory T cells. Blood. 2007; 110 (10): 3793–803. DOI: 10.1182/blood-2007-04-086470.
8. Hadeiba H., Lahl K., Edalati A., Oderup C., Habtezion A., Pachynski R., et al. Plasmacytoid dendritic cells transport peripheral antigens to the thymus to promote central tolerance. Immunity. 2012; 36 (3): 438–50. DOI: 10.1016/j.immuni.2012.01.017.
9. Hadeiba H., Sato T., Habtezion A., Oderup C., Pan J., Butcher E. CCR9 expression defines tolerogenic plasmacytoid dendritic cells able to suppress acute graft-versus-host disease. Nat. Immunol. 2008; 9 (11): 1253–60. DOI: 10.1038/ni.1658.
10. Mach N., Gillessen S., Wilson S., Sheehan C., Mihm M., Dranoff G. Differences in dendritic cells stimulated in vivo by tumors engineered to secrete granulocyte-macrophage colony-stimulating factor or Flt3-ligand. Cancer Res. 2000; 60: 3239–46.
11. Wendland M., Czeloth N., Mach N., Malissen B., Kremmer E., Pabst O., et al. CCR9 is a homing receptor for plasmacytoid dendritic cells to the small intestine. Proc. Natl Acad. Sci. USA. 2007; 104 (15): 6347–52. DOI: 10.1073/pnas.0609180104.
12. Zeng R., Oderup C., Yuan R., Lee M., Habtezion A., Hadeiba H., et al. Retinoic acid regulates the development of a gut-homing precursor for intestinal dendritic cells. Mucosal Immunol. 2013; 6 (4): 847–56. DOI: 10.1038/mi.2012.123.
13. Chen Y., Chang S., Chen T., Lee C. Efficient generation of plasmacytoid dendritic cell from common lymphoid progenitors by Flt3 ligand. PLoS One. 2015; 10 (8): e0135217. DOI: 10.1371/journal.pone.0135217.
14. Liu H., Ramachandran I., Gabrilovich D.I. Regulation of plasmacytoid dendritic cell development in mice by aryl hydrocarbon receptor. Immunol. Cell Biol. 2014; 92 (2): 200–3. DOI: 10.1038/icb.2013.65.
15. Brawand P., Fitzpatrick D. R., Greenfield B., Brasel K., Maliszewski C., De Smedt T. Murine plasmacytoid pre-dendritic cells generated from Flt3 ligand-supplemented bone marrow cultures are immature APCs. J. Immunol. 2002; 169 (12): 6711–9.
16. Angelov G. S., Tomkowiak M., Marcais A., Leverrier Y., Marvel J. Flt3 ligand-generated murine plasmacytoid and conventional dendritic cells differ in their capacity to prime naive CD8 T cells and to generate memory cells in vivo. J. Immunol. 2005; 175 (1): 189–95.
17. Feng T., Cong Y., Qin H., Benveniste E., Elson C. Generation of mucosal dendritic cells from bone marrow reveals a critical role of retinoic acid. J. Immunol. 2010; 185 (10): 5915–25. DOI: 10.4049/jimmunol.1001233.
18. Karrich J., Jachimowski L., Uittenbogaart C., Blom B. The plasmacytoid dendritic cell as the Swiss army knife of the immune system: molecular regulation of its multifaceted functions. J. Immunol. 2014; 193 (12): 5772–8. DOI: 10.4049/jimmunol.1401541.
19. Funderburg N., Lederman M., Feng Z., Drage M., Jadlowsky J., Harding C., et al. Human-defensin-3 activates professional antigen-presenting cells via Toll-like receptors 1 and 2. Proc. Natl Acad. Sci. USA. 2007; 104 (47): 18 631–5.
20. Bhattacharya P., Gopisetty A., Ganesh B., Sheng J., Prabhakar B. GM-CSF-induced, bone-marrow-derived dendritic cells can expand natural Tregs and induce adaptive Tregs by different mechanisms. J. Leukoc. Biol. 2011; 89: 235–49.
21. Muller G., Hopken U., Stein H., Lipp M. Systemic immunoregulatory and pathogenic functions of homeostatic chemokine receptors. J. Leukoc. Biol. 2002; 72 (1): 1–8.
22. Syrovatkina V., Alegre K., Dey R., Huang X. Regulation, signaling, and physiological functions of G-proteins. J. Mol. Biol. 2016; 428 (19): 3850–68. DOI: 10.1016/j.jmb.2016.08.002
23. Lee H., Kim H., Lee E., Jang M., Kim S., Park J., et al. Characterization of CCR9 expression and thymus-expressed chemokine responsiveness of the murine thymus, spleen and mesenteric lymph node. Immunobiology. 2012; 217 (4): 402–11. DOI: 10.1016/j.imbio.2011.10.014.