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Critical Reviews™ in Immunology

Published 6 issues per year

ISSN Print: 1040-8401

ISSN Online: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

Indexed in

Regulation of Antigen-Specific Regulatory T-Cell Induction via Nasal and Oral Mucosa

Volume 24, Issue 3, 2004, 22 pages
DOI: 10.1615/CritRevImmunol.v24.i3.10
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ABSTRACT

With the identification of regulatory T cells (Tr), the hunt for ways to specifically intervene in ongoing inflammatory responses has grown exponentially. Tr are attractive for therapy because they have the potential to control deleterious responses while preserving normal immune function. It has long been known that application of soluble antigen via the mucosa induces mucosal Tr that preserve systemic tolerance upon challenge with the same antigen. Mucosal Tr exhibit three major properties that allow selective control of immune responses. They are (1) adaptive—that is, they differentiate from naive T cells in the periphery; (2) antigen-specific—that is, specific for the (exogenous) antigen applied via the mucosa; and (3) versatile—that is, suppress, irrespective of ongoing Th1 or Th2 cytokine polarization. These powerful characteristics provide mucosal Tr with all requirements necessary to selectively interfere in an unbalanced immune system, as occurs in diseases ranging from autoimmunity to transplant rejection and allergy. Until now, however, translation into clinical applications has led to moderate success. This is primarily due to limited knowledge about the fundamental characteristics of these cells because of the lack of a differential marker. The initial stages of mucosal Tr induction, which may hold the key to discovering the identity of mucosal Tr and unraveling their function, are discussed in this review.

CITED BY
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  3. van Wijk F., Wehrens E. J. M., Nierkens S., Boon L., Kasran A., Pieters R., Knippels L. M. J., CD4+CD25+T cells regulate the intensity of hypersensitivity responses to peanut, but are not decisive in the induction of oral sensitization, Clinical & Experimental Allergy, 37, 4, 2007. Crossref

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  6. Novak Natalija, Haberstok Jörg, Bieber Thomas, Allam Jean-Pierre, The immune privilege of the oral mucosa, Trends in Molecular Medicine, 14, 5, 2008. Crossref

  7. Kabelitz Dieter, Geissler Edward K., Soria Bernat, Schroeder Insa S., Fändrich Fred, Chatenoud Lucienne, Toward cell-based therapy of type I diabetes, Trends in Immunology, 29, 2, 2008. Crossref

  8. Li Haiyu, Ding Yanping, Yi Guiwen, Zeng Qiutang, Yang Wenkai, Establishment of nasal tolerance to heat shock protein-60 alleviates atherosclerosis by inducing TGF-β-dependent regulatory T cells, Journal of Huazhong University of Science and Technology [Medical Sciences], 32, 1, 2012. Crossref

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  10. Birmingham Janette M., Patil Sangita, Li Xiu-Min, Busse Paula J., The Effect of Oral Tolerance on the Allergic Airway Response in Younger and Aged Mice, Journal of Asthma, 50, 2, 2013. Crossref

  11. Slütter Bram, Jiskoot Wim, Dual role of CpG as immune modulator and physical crosslinker in ovalbumin loaded N-trimethyl chitosan (TMC) nanoparticles for nasal vaccination, Journal of Controlled Release, 148, 1, 2010. Crossref

  12. Rossi Oriana, van Berkel Lisette A., Chain Florian, Tanweer Khan M., Taverne Nico, Sokol Harry, Duncan Sylvia H., Flint Harry J., Harmsen Hermie J. M., Langella Philippe, Samsom Janneke N., Wells Jerry M., Faecalibacterium prausnitzii A2-165 has a high capacity to induce IL-10 in human and murine dendritic cells and modulates T cell responses, Scientific Reports, 6, 1, 2016. Crossref

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  14. Howe Savannah, Sowa Gavin, Konjufca Vjollca, Systemic and Mucosal Antibody Responses to Soluble and Nanoparticle-Conjugated Antigens Administered Intranasally, Antibodies, 5, 4, 2016. Crossref

  15. Li Xinhui, Johnson Kory R., Bryant Mark, Elkahloun Abdel G., Amar Marcelo, Remaley Alan T., De Silva Ranil, Hallenbeck John M., Quandt Jacqueline A., Zernecke Alma, Intranasal Delivery of E-Selectin Reduces Atherosclerosis in ApoE−/− Mice, PLoS ONE, 6, 6, 2011. Crossref

  16. Chebotareva Natalia, Bobkova Irina, Shilov Evgeniy, Heat shock proteins and kidney disease: perspectives of HSP therapy, Cell Stress and Chaperones, 22, 3, 2017. Crossref

  17. Allam Jean-Pierre, Novak Natalija, Mucosal Homeostasis of the Oral Mucosa, in Oral Mucosa in Health and Disease, 2018. Crossref

  18. Lund Kaare, Kito Hirokazu, Skydtsgaard Mette Blem, Nakazawa Hiroshi, Ohashi-Doi Katsuyo, Lawton Simon, The Importance of Tablet Formulation on Allergen Release Kinetics and Efficiency: Comparison of Freeze-dried and Compressed Grass Pollen Sublingual Allergy Immunotherapy Tablet Formulations, Clinical Therapeutics, 41, 4, 2019. Crossref

  19. Broere Femke, Wieten Lotte, Klein Koerkamp Elles I., van Roon Joel A. G., Guichelaar Teun, Lafeber Floris P. J. G., van Eden Willem, Oral or Nasal Antigen Induces Regulatory T Cells That Suppress Arthritis and Proliferation of Arthritogenic T Cells in Joint Draining Lymph Nodes, The Journal of Immunology, 181, 2, 2008. Crossref

  20. Samsom Janneke N., van der Marel Arnold P. J., van Berkel Lisette A., van Helvoort Joop M. L. M., Simons-Oosterhuis Ytje, Jansen Wendy, Greuter Mascha, Nelissen Rob L. H., Meeuwisse Cees M. L., Nieuwenhuis Edward E. S., Mebius Reina E., Kraal Georg, Secretory Leukoprotease Inhibitor in Mucosal Lymph Node Dendritic Cells Regulates the Threshold for Mucosal Tolerance, The Journal of Immunology, 179, 10, 2007. Crossref

  21. Hasselberg Annemarie, Ekman Lena, Yrlid Linda Fahlén, Schön Karin, Lycke Nils Y., ADP-Ribosylation Controls the Outcome of Tolerance or Enhanced Priming Following Mucosal Immunization, The Journal of Immunology, 184, 6, 2010. Crossref

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