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      ICON: chronic rhinosinusitis

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          Abstract

          Chronic rhinosinusitis (CRS) is a public health problem that has a significant socio-economic impact. Moreover, the complexity of this disease due to its heterogeneous nature based on the underlying pathophysiology - leading to different disease variants - further complicates our understanding and directions for the most appropriate targeted treatment strategies. Several International/national guidelines/position papers and/or consensus documents are available that present the current knowledge and treatment strategies for CRS. Yet there are many challenges to the management of CRS especially in the case of the more severe and refractory forms of disease. Therefore, the International Collaboration in Asthma, Allergy and Immunology (iCAALL), a collaboration between EAACI, AAAAI, ACAAI, and WAO, has decided to propose an International Consensus (ICON) on Chronic Rhinosinusitis. The purpose of this ICON on CRS is to highlight the key common messages from the existing guidelines, the differences in recommendations as well as the gaps in our current knowledge of CRS, thus providing a concise reference. In this document we discuss the definition of the disease, its relevance, pharmacoeconomics, pathophysiology, phenotypes and endotypes, genetics and risk factors, natural history and co-morbidities as well as clinical manifestations and treatment options in both adults and children comprising pharmacotherapy, surgical interventions and more recent biological approaches. Finally, we have also highlighted the unmet needs that wait to be addressed through future research.

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          Most cited references327

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          Persister cells, dormancy and infectious disease.

          Kim Lewis (2007)
          Several well-recognized puzzles in microbiology have remained unsolved for decades. These include latent bacterial infections, unculturable microorganisms, persister cells and biofilm multidrug tolerance. Accumulating evidence suggests that these seemingly disparate phenomena result from the ability of bacteria to enter into a dormant (non-dividing) state. The molecular mechanisms that underlie the formation of dormant persister cells are now being unravelled and are the focus of this Review.
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            EPOS 2012: European position paper on rhinosinusitis and nasal polyps 2012. A summary for otorhinolaryngologists

            The European Position Paper on Rhinosinusitis and Nasal Polyps 2012 is the update of similar evidence based position papers published in 2005 and 2007. The document contains chapters on definitions and classification, we now also proposed definitions for difficult to treat rhinosinusitis, control of disease and better definitions for rhinosinusitis in children. More emphasis is placed on the diagnosis and treatment of acute rhinosinusitis. Throughout the document the terms chronic rhinosinusitis without nasal polyps (CRSsNP) and chronic rhinosinusitis with nasal polyps (CRSwNP) are used to further point out differences in pathophysiology and treatment of these two entities. There are extensive chapters on epidemiology and predisposing factors, inflammatory mechanisms, (differential) diagnosis of facial pain, genetics, cystic fibrosis, aspirin exacerbated respiratory disease, immunodeficiencies, allergic fungal rhinosinusitis and the relationship between upper and lower airways. The chapters on paediatric acute and chronic rhinosinusitis are totally rewritten. Last but not least all available evidence for management of acute rhinosinusitis and chronic rhinosinusitis with or without nasal polyps in adults and children is analyzed and presented and management schemes based on the evidence are proposed. This executive summary for otorhinolaryngologists focuses on the most important changes and issues for otorhinolaryngologists. The full document can be downloaded for free on the website of this journal: http://www.rhinologyjournal.com.
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              Human IL-25- and IL-33-responsive type 2 innate lymphoid cells are defined by expression of CRTH2 and CD161.

              Innate lymphoid cells (ILCs) are emerging as a family of effectors and regulators of innate immunity and tissue remodeling. Interleukin 22 (IL-22)- and IL-17-producing ILCs, which depend on the transcription factor RORγt, express CD127 (IL-7 receptor α-chain) and the natural killer cell marker CD161. Here we describe another lineage-negative CD127(+)CD161(+) ILC population found in humans that expressed the chemoattractant receptor CRTH2. These cells responded in vitro to IL-2 plus IL-25 and IL-33 by producing IL-13. CRTH2(+) ILCs were present in fetal and adult lung and gut. In fetal gut, these cells expressed IL-13 but not IL-17 or IL-22. There was enrichment for CRTH2(+) ILCs in nasal polyps of chronic rhinosinusitis, a typical type 2 inflammatory disease. Our data identify a unique type of human ILC that provides an innate source of T helper type 2 (T(H)2) cytokines.
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                Author and article information

                Contributors
                Claus.Bachert@ugent.be
                pawankar.ruby@gmail.com
                Dr.LuoZhang@gmail.com
                Chaweewan.Bun@mahidol.ac.th
                W.J.Fokkens@amc.uva.nl
                dhamilos@partners.org
                siojr@mahidol.ac.th
                RKern@nmff.org
                eomeltzer@aol.com
                jmullol@clinic.ub.es
                rnacleri@surgery.bsd.uchicago.edu
                renatapilan.orl@gmail.com
                csrhee@snu.ac.kr
                h-suzaki@med.showa-u.ac.jp
                rvoegels@gmail.com
                mblaiss@allergymemphis.com
                Journal
                World Allergy Organ J
                World Allergy Organ J
                The World Allergy Organization Journal
                BioMed Central (London )
                1939-4551
                27 October 2014
                27 October 2014
                2014
                : 7
                : 1
                : 25
                Affiliations
                [ ]Upper Airways Research Laboratory (URL), University Hospital Ghent, Kragujevac, Belgium
                [ ]Div. of Allergy, Dept. of Pediatrics, Nippon Medical School, Tokyo, Japan
                [ ]Beijing Key Laboratory of Nasal diseases, Beijing Institute of Otolaryngology, Beijing, China
                [ ]Faculty of Medicine, Siriraj Hospital Mahidol University, Bangkok, Thailand
                [ ]Department of Otorhinolaryngology, Academic Medical Centre, Amsterdam, The Netherlands
                [ ]Division of Rheumatology, Allergy & Immunology, Massachusetts General Hospital, Boston, MA USA
                [ ]Department of Otolaryngology Head and Neck Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois USA
                [ ]Allergy & Asthma Medical Group & Research Center, San Diego, California USA
                [ ]Rhinology Unit & Smell Clinic, Hospital Clínic – IDIBAPS, Barcelona, Catalonia Spain
                [ ]Section of Otolaryngology Head and Neck Surgery, Department of Surgery, University of Chicago, Chicago, Illinois USA
                [ ]Department of Otorhinolaryngology, Clinics Hospital/University of Sao Paulo Medical School, Kragujevac, Brazil
                [ ]Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University Bundang Hospital, Seongnam, Seoul National University College of Medicine, Seoul, Korea
                [ ]Dept. of Otorhinolaryngology, Showa University, Tokyo, Japan
                [ ]Department of Rhinology, University of Sao Paulo Medical School, Sao Paulo, Brazil
                [ ]University of Tennessee Health Science Center, Memphis, Tennessee
                Article
                69
                10.1186/1939-4551-7-25
                4213581
                25379119
                85b121a8-5d50-474b-888f-5a7aa92a1d66
                © Bachert et al.; licensee BioMed Central Ltd. 2014

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 27 August 2014
                : 27 August 2014
                Categories
                Consensus Document
                Custom metadata
                © The Author(s) 2014

                Immunology
                chronic rhinosinusitis,pharmacoeconomics,pathophysiology,phenotypes,genetics,co-morbidities,treatment,biologicals,unmet needs

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