CD207+ cells recruitment to the vaccination site and draining lymph nodes after the administration of DC-Apo/Nec vaccine in mice

De novo ectopic lymphoid tissue formation is known to occur in certain disease and inflammatory settings. After an effective vaccination with dendritic cells (DC) charged with melanoma apoptotic/necrotic cells (Apo/Nec), a subcutaneous tertiary lymphoid structure was organized, where retained vaccin...

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Autor principal: Ruiz, M.S
Otros Autores: Mac Keon, S., Campisano, S., Bravo, A.I, Gazzaniga, S., Wainstok, Rosa
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2014
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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100 1 |a Ruiz, M.S. 
245 1 0 |a CD207+ cells recruitment to the vaccination site and draining lymph nodes after the administration of DC-Apo/Nec vaccine in mice 
260 |c 2014 
270 1 0 |m Gazzaniga, S.; Faculty of Sciences, University of Buenos Aires, Biochemistry Department, Intendente Güiraldes 2160, C1428EGA Ciudad Autónoma de Buenos Aires, Argentina; email: sgazza@qb.fcen.uba.ar 
504 |a Steinman, R.M., Dendritic cells in vivo: a key target for a new vaccine science (2008) Immunity, 29, pp. 319-324 
504 |a Schuler-Thurner, B., Rapid induction of tumor-specific type 1 T helper cells in metastatic melanoma patients by vaccination with mature, cryopreserved, peptide-loaded monocyte-derived dendritic cells (2002) Journal of Experimental Medicine, 195, pp. 1279-1288 
504 |a Goldszmid, R.S., Idoyaga, J., Bravo, A.I., Steinman, R., Mordoh, J., Wainstok, R., Dendritic cells charged with apoptotic tumor cells induce long-lived protective CD4+ and CD8+ T cell immunity against B16 melanoma (2003) Journal of Immunology (Baltimore MD: 1950), 171, pp. 5940-5947 
504 |a Mac Keon, S., Gazzaniga, S., Mallerman, J., Bravo, A.I., Mordoh, J., Wainstok, R., Vaccination with dendritic cells charged with apoptotic/necrotic B16 melanoma induces the formation of subcutaneous lymphoid tissue (2010) Vaccine, 28, pp. 8162-8168 
504 |a Ali, O.A., Emerich, D., Dranoff, G., Mooney, D.J., In situ regulation of DC subsets and T cells mediates regression in mice (2009) Science Translational Medicine, 1, pp. 1-22 
504 |a Henri, S., Poulin, L.F., Tamoutounour, S., Ardouin, L., Guilliams, M., De Bovis, B., CD207+ CD103+ dermal dendritic cells cross-present keratinocyte-derived antigens irrespective of the presence of Langerhans cells (2010) Journal of Experimental Medicine, 207, pp. 189-206 
504 |a Stoecklinger, A., Eticha, T.D., Mesdaghi, M., Kissenpfennig, A., Malissen, B., Thalhamer, J., Langerin+ dermal dendritic cells are critical for CD8 T cell activation and IgH γ-1 class switching in response to gene gun vaccines (2011) Journal of Immunology (Baltimore, MD: 1950), 186, pp. 1377-1383 
504 |a Kissenpfennig, A., Henri, S., Dubois, B., Laplace-Builhé, C., Perrin, P., Romani, N., Dynamics and function of Langerhans cells in vivo: dermal dendritic cells colonize lymph node areas distinct from slower migrating Langerhans cells (2005) Immunity, 22, pp. 643-654 
504 |a Sixt, M., Kanazawa, N., Selg, M., Samson, T., Roos, G., Reinhardt, D.P., The conduit system transports soluble antigens from the afferent lymph to resident dendritic cells in the T cell area of the lymph node (2005) Immunity, 22, pp. 19-29 
504 |a Flacher, V., Tripp, C.H., Stoitzner, P., Haid, B., Ebner, S., Del Frari, B., Epidermal Langerhans cells rapidly capture and present antigens from C-type lectin-targeting antibodies deposited in the dermis (2010) Journal of Investigative Dermatology, 130, pp. 755-762 
504 |a Singh-Jasuja, H., Thiolat, A., Ribon, M., Boissier, M.-C., Bessis, N., Rammensee, H.-G., The mouse dendritic cell marker CD11c is down-regulated upon cell activation through Toll-like receptor triggering (2013) Immunobiology, 218, pp. 28-39 
504 |a Geissmann, F., Dieu-Nosjean, M.C., Dezutter, C., Valladeau, J., Kayal, S., Leborgne, M., Accumulation of immature Langerhans cells in human lymph nodes draining chronically inflamed skin (2002) Journal of Experimental Medicine, 196, pp. 417-430 
504 |a Chalermsarp, N., Azuma, M., Identification of three distinct subsets of migrating dendritic cells from oral mucosa within the regional lymph nodes (2009) Immunology, 127, pp. 558-566 
504 |a Douillard, P., Stoitzner, P., Tripp, C.H., Clair-Moninot, V., Aït-Yahia, S., McLellan, A.D., Mouse lymphoid tissue contains distinct subsets of langerin/CD207 dendritic cells, only one of which represents epidermal-derived Langerhans cells (2005) Journal of Investigative Dermatology, 125, pp. 983-994 
506 |2 openaire  |e Política editorial 
520 3 |a De novo ectopic lymphoid tissue formation is known to occur in certain disease and inflammatory settings. After an effective vaccination with dendritic cells (DC) charged with melanoma apoptotic/necrotic cells (Apo/Nec), a subcutaneous tertiary lymphoid structure was organized, where retained vaccine cells interacted with recruited inflammatory and T cells. In this work we report for the first time the recruitment of two morphologically different CD207+ cells to vaccination site. The time-course behavior of CD207+ cells was reciprocal between vaccination site and draining lymph nodes (DLNs). After 6-10 days, CD207+ cells localized at the paracortical region of DLNs, in close contact with T cell population. DLNs were enriched in a peculiar MHCII+ CD11c(-) CD207+ population, whose role remains to be determined. Whether CD207+ cells migration to the vaccination site can be associated with a differential anti-tumoral response remains as an open and exciting question. © 2014 Elsevier Ltd.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, PICT0010 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: This work was supported by grants from the following institutions: University of Buenos Aires, Agencia Nacional de Promoción Científica y Tecnológica ( PICT0010 ) and CONICET. We thank Dr. José Mordoh for carefully reading this manuscript. Appendix A 
593 |a Dpto. de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina 
593 |a Fundación Instituto Leloir, IIBBA CONICET, Buenos Aires, Argentina 
593 |a Hospital Eva Perón, San Martín, Buenos Aires, Argentina 
690 1 0 |a CD207+ CELLS 
690 1 0 |a DENDRITIC CELLS 
690 1 0 |a ECTOPIC LYMPHOID TISSUE 
690 1 0 |a MELANOMA 
690 1 0 |a VACCINE 
690 1 0 |a CD207(+) CELLS 
690 1 0 |a DENDRITIC CELLS 
690 1 0 |a ECTOPIC LYMPHOID TISSUE 
690 1 0 |a MELANOMA 
690 1 0 |a VACCINE 
690 1 0 |a ANIMALS 
690 1 0 |a ANTIGENS, SURFACE 
690 1 0 |a CANCER VACCINES 
690 1 0 |a CELL MOVEMENT 
690 1 0 |a DENDRITIC CELLS 
690 1 0 |a LECTINS, C-TYPE 
690 1 0 |a LYMPH NODES 
690 1 0 |a LYMPHOID TISSUE 
690 1 0 |a MANNOSE-BINDING LECTINS 
690 1 0 |a MELANOMA 
690 1 0 |a MICE 
690 1 0 |a MICE, INBRED C57BL 
690 1 0 |a T-LYMPHOCYTES 
700 1 |a Mac Keon, S. 
700 1 |a Campisano, S. 
700 1 |a Bravo, A.I. 
700 1 |a Gazzaniga, S. 
700 1 |a Wainstok, Rosa 
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