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Tolerogenic Dendritic Cells
Abstract
▪ Abstract Dendritic cells (DCs) have several functions in innate and adaptive immunity. In addition, there is increasing evidence that DCs in situ induce antigen-specific unresponsiveness or tolerance in central lymphoid organs and in the periphery. In the thymus DCs generate tolerance by deleting self-reactive T cells. In peripheral lymphoid organs DCs also induce tolerance to antigens captured by receptors that mediate efficient uptake of proteins and dying cells. Uptake by these receptors leads to the constitutive presentation of antigens on major histocompatibility complex (MHC) class I and II products. In the steady state the targeting of DC antigen capture receptors with low doses of antigens leads to deletion of the corresponding T cells and unresponsiveness to antigenic rechallenge with strong adjuvants. In contrast, if a stimulus for DC maturation is coadministered with the antigen, the mice develop immunity, including interferon-γ-secreting effector T cells and memory T cells. There is also new evidence that DCs can contribute to the expansion and differentiation of T cells that regulate or suppress other immune T cells. One possibility is that distinct developmental stages and subsets of DCs and T cells can account for the different pathways to peripheral tolerance, such as deletion or suppression. We suggest that several clinical situations, including autoimmunity and certain infectious diseases, can be influenced by the antigen-specific tolerogenic role of DCs.
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Cites
Cross-Presentation, Dendritic Cells, Tolerance and Immunity
Heath, W. R., & Carbone, F. R. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.47 · Cited by 882
BH3-only Bcl-2 family member Bim is required for apoptosis of autoreactive thymocytes
Bouillet, P., Purton, J. F., Godfrey, D. I., Zhang, L.-C., Coultas, L., Puthalakath, H., Pellegrini, M., Cory, S., Adams, J. M., & Strasser, A. (2002) · Nature · doi:10.1038/415922a · Cited by 782
Linehan, S. A., Martínez-Pomares, L., Stahl, P. D., & Gordon, S. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.12.1961 · Cited by 285
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Green, D. R., Ferguson, T., Zitvogel, L., & Kroemer, G. (2009) · Nature Reviews Immunology · doi:10.1038/nri2545 · Cited by 1,176
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Diamond, M. S., Kinder, M., Matsushita, H., Mashayekhi, M., Dunn, G. P., Archambault, J. M., Lee, H., Arthur, C. D., White, J. M., Kalinke, U., et al. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20101158 · Cited by 1,081
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Merad, M., Ginhoux, F., & Collin, M. (2008) · Nature Reviews Immunology · doi:10.1038/nri2455 · Cited by 850
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Kazama, H., Ricci, J.-E., Herndon, J. M., Hoppe, G., Green, D. R., & Ferguson, T. A. (2008) · Immunity · doi:10.1016/j.immuni.2008.05.013 · Cited by 627
Schmid, D., Pypaert, M., & Münz, C. (2007) · Immunity · doi:10.1016/j.immuni.2006.10.018 · Cited by 577
Liang, B., Workman, C., Lee, J., Chew, C., Dale, B. M., Colonna, L., Flores, M., Li, N., Schweighoffer, E., Greenberg, S., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.9.5916 · Cited by 566
Guiducci, C., Vicari, A. P., Sangaletti, S., Trinchieri, G., & Colombo, M. P. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-4262 · Cited by 549
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Trapp, S., Derby, N. R., Singer, R., Shaw, A., Williams, V. G., Turville, S. G., Bess, J. W., Lifson, J. D., & Robbiani, M. (2009) · Journal of Virology · doi:10.1128/jvi.00023-08 · Cited by 79
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Varikuti, S., Singh, B., Volpedo, G., Ahirwar, D. K., Jha, B. K., Saljoughian, N., Viana, A. G., Verma, C., Hamza, O., Halsey, G., et al. (2020) · British Journal of Cancer · doi:10.1038/s41416-020-0743-8 · Cited by 76
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Dendritic cell responses to surface properties of clinical titanium surfaces
Kou, P. M., Schwartz, Z., Boyan, B. D., & Babensee, J. E. (2011) · Acta Biomaterialia · doi:10.1016/j.actbio.2010.10.020 · Cited by 73
Zacca, E. R., Crespo, M. I., Acland, R. P., Roselli, E., Núñez, N. G., Maccioni, M., Maletto, B. A., Pistoresi-Palencia, M. C., & Morón, G. (2015) · PLOS ONE · doi:10.1371/journal.pone.0140672 · Cited by 66
Zhang, A.-H., Rossi, R. J., Yoon, J., Wang, H., & Scott, D. W. (2016) · Cellular Immunology · doi:10.1016/j.cellimm.2015.11.004 · Cited by 65
Nielsen, H. S., Steffensen, R., Lund, M., Egestad, L., Mortensen, L. H., Andersen, A. M. N., Lidegaard, O., & Christiansen, O. B. (2010) · Human Reproduction · doi:10.1093/humrep/deq091 · Cited by 61
Fong, F. L. Y., Kirjavainen, P. V., & El-Nezami, H. (2016) · Scientific Reports · doi:10.1038/srep22845 · Cited by 56
Luo, L., Qin, T., Huang, Y., Zheng, S., Bo, R., Liu, Z., Xing, J., Hu, Y., Liu, J., & Wang, D. (2017) · Drug Delivery · doi:10.1080/10717544.2017.1359861 · Cited by 47
Osteoprotegerin expression in dendritic cells increases with maturation and is NF‐κB‐dependent
Schoppet, M., Henser, S., Ruppert, V., Stübig, T., Al‐Fakhri, N., Maisch, B., & Hofbauer, L. C. (2007) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21129 · Cited by 45
Dumortier, H., van Mierlo, G. J. D., Egan, D., van Ewijk, W., Toes, R. E. M., Offringa, R., & Melief, C. J. M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.2.855 · Cited by 39
Li, Y., Heuser, J. S., Kosanke, S. D., Hemric, M., & Cunningham, M. W. (2005) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)62948-3 · Cited by 39
Herndon, J. M., Stuart, P. M., & Ferguson, T. A. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.7.4098 · Cited by 38
Fasciola hepatica immune regulates CD11c+ cells by interacting with the macrophage Gal/GalNAc lectin
Rodríguez, E., Carasi, P., Frigerio, S., da Costa, V., van Vliet, S., Noya, V., Brossard, N., van Kooyk, Y., García-Vallejo, J. J., & Freire, T. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00264 · Cited by 36
Absence of Immune Responses with Xenogeneic Collagen and Elastin
Bayrak, A., Prüger, P., Stock, U. A., & Seifert, M. (2013) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0394 · Cited by 35
Hontelez, S., Karthaus, N., Looman, M. W., Ansems, M., & Adema, G. J. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201776 · Cited by 35
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Humbert, M., Hugues, S., & Dubrot, J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00684 · Cited by 32
Popov, A., Driesen, J., Abdullah, Z., Wickenhauser, C., Beyer, M., Debey-Pascher, S., Saric, T., Kummer, S., Takikawa, O., Domann, E., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.7.4976 · Cited by 32
Natural killer cells become tolerogenic after interaction with apoptotic cells
Chong, W. P., Zhou, J., Law, H. K. W., Tu, W., & Lau, Y. L. (2010) · European Journal of Immunology · doi:10.1002/eji.200939768 · Cited by 22
Darvekar, S., Juzenas, P., Oksvold, M., Kleinauskas, A., Holien, T., Christensen, E., Stokke, T., Sioud, M., & Peng, Q. (2020) · Cancers · doi:10.3390/cancers12020377 · Cited by 16
Valaperti, A., Nishii, M., Germano, D., Liu, P. P., & Eriksson, U. (2013) · Vaccine · doi:10.1016/j.vaccine.2013.07.084 · Cited by 15
Metadata
- Authors
- Steinman, R. M., Hawiger, D., & Nussenzweig, M. C.
- Venue
- Annual Review of Immunology
- Publisher
- Annual Reviews
- Published
- 2003-04
- Volume
- 21
- Issue
- 1
- Pages
- 685-711
- ISSN
- 0732-0582 (ISSN-L)
- 1545-3278
- OpenAlex
- W2161354474
- Cited by
- 3,122
- References
- 3
- FWCI
- 10.12
- Type
- journal article
- Language
- en
- Open access
- closed
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