Specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after allergen challenge chamber exposure

Abstract Background Allergic rhinitis is an inflammatory disease that causes cellular influx and mediator release in the nose. These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments. Objective To assess the specificity and reproducibilit...

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Veröffentlicht in:Annals of allergy, asthma, & immunology asthma, & immunology, 2017-03, Vol.118 (3), p.290-297
Hauptverfasser: Badorrek, Philipp, MD, Müller, Meike, PhD, Koch, Wolfgang, PhD, Hohlfeld, Jens M., MD, Krug, Norbert, MD
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container_issue 3
container_start_page 290
container_title Annals of allergy, asthma, & immunology
container_volume 118
creator Badorrek, Philipp, MD
Müller, Meike, PhD
Koch, Wolfgang, PhD
Hohlfeld, Jens M., MD
Krug, Norbert, MD
description Abstract Background Allergic rhinitis is an inflammatory disease that causes cellular influx and mediator release in the nose. These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments. Objective To assess the specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after grass pollen exposure in an allergen challenge chamber. Methods In a monocenter pilot study, 15 patients with allergic rhinitis and 19 healthy individuals underwent two 4-hour Dactylis glomerate pollen challenges in the challenge chamber with an interval of 21 days. Before challenge, on exit, and after 2 and 22 hours, a nasal lavage was performed and nasal secretions were collected on filter paper to determine a wide panel of cells and mediators. Furthermore, total nasal symptom score, nasal flow, and nasal nitric oxide were measured. Results Pollen exposure significantly increased eosinophil, interleukin (IL) 5, IL-6, IL-13, and macrophage inflammatory protein 1β levels in allergic patients but not in healthy individuals. The effect could be reproduced for eosinophils, IL-5, IL-6, and macrophage inflammatory protein 1β after the second allergen challenge. By contrast, the IL-13 levels were higher and eotaxin levels first increased after repetitive allergen challenge. There was no correlation between total nasal symptom score and elevated cell or cytokine levels. Nasal nitric oxide levels were nonspecifically elevated in both patients with allergy and healthy controls. Conclusion A subset of cellular and soluble biomarkers in nasal lavage and secretion reveals specificity and reproducibility in patients with allergic rhinitis. These can be used to measure the immunologic efficacy of antiallergic treatments in an allergen challenge chamber. Carryover effects attributable to priming must be considered when designing cross-over studies. Trial Registration clinicaltrials.gov Identifier: NCT00297843.
doi_str_mv 10.1016/j.anai.2017.01.018
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These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments. Objective To assess the specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after grass pollen exposure in an allergen challenge chamber. Methods In a monocenter pilot study, 15 patients with allergic rhinitis and 19 healthy individuals underwent two 4-hour Dactylis glomerate pollen challenges in the challenge chamber with an interval of 21 days. Before challenge, on exit, and after 2 and 22 hours, a nasal lavage was performed and nasal secretions were collected on filter paper to determine a wide panel of cells and mediators. Furthermore, total nasal symptom score, nasal flow, and nasal nitric oxide were measured. Results Pollen exposure significantly increased eosinophil, interleukin (IL) 5, IL-6, IL-13, and macrophage inflammatory protein 1β levels in allergic patients but not in healthy individuals. The effect could be reproduced for eosinophils, IL-5, IL-6, and macrophage inflammatory protein 1β after the second allergen challenge. By contrast, the IL-13 levels were higher and eotaxin levels first increased after repetitive allergen challenge. There was no correlation between total nasal symptom score and elevated cell or cytokine levels. Nasal nitric oxide levels were nonspecifically elevated in both patients with allergy and healthy controls. Conclusion A subset of cellular and soluble biomarkers in nasal lavage and secretion reveals specificity and reproducibility in patients with allergic rhinitis. These can be used to measure the immunologic efficacy of antiallergic treatments in an allergen challenge chamber. Carryover effects attributable to priming must be considered when designing cross-over studies. Trial Registration clinicaltrials.gov Identifier: NCT00297843.</description><identifier>ISSN: 1081-1206</identifier><identifier>EISSN: 1534-4436</identifier><identifier>DOI: 10.1016/j.anai.2017.01.018</identifier><identifier>PMID: 28284536</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Allergens - immunology ; Allergy and Immunology ; Biomarkers ; Case-Control Studies ; Cytokines - metabolism ; Female ; Humans ; Immunization ; Inflammation Mediators - metabolism ; Leukocyte Count ; Male ; Nasal Lavage Fluid - immunology ; Nasal Mucosa - immunology ; Nasal Mucosa - metabolism ; Nasal Provocation Tests ; Nitric Oxide - metabolism ; Pilot Projects ; Pollen - immunology ; Rhinitis, Allergic - diagnosis ; Rhinitis, Allergic - immunology ; Rhinitis, Allergic - metabolism ; Rhinomanometry ; Severity of Illness Index ; Young Adult</subject><ispartof>Annals of allergy, asthma, &amp; immunology, 2017-03, Vol.118 (3), p.290-297</ispartof><rights>American College of Allergy, Asthma &amp; Immunology</rights><rights>2017 American College of Allergy, Asthma &amp; Immunology</rights><rights>Copyright © 2017 American College of Allergy, Asthma &amp; Immunology. Published by Elsevier Inc. 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These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments. Objective To assess the specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after grass pollen exposure in an allergen challenge chamber. Methods In a monocenter pilot study, 15 patients with allergic rhinitis and 19 healthy individuals underwent two 4-hour Dactylis glomerate pollen challenges in the challenge chamber with an interval of 21 days. Before challenge, on exit, and after 2 and 22 hours, a nasal lavage was performed and nasal secretions were collected on filter paper to determine a wide panel of cells and mediators. Furthermore, total nasal symptom score, nasal flow, and nasal nitric oxide were measured. Results Pollen exposure significantly increased eosinophil, interleukin (IL) 5, IL-6, IL-13, and macrophage inflammatory protein 1β levels in allergic patients but not in healthy individuals. The effect could be reproduced for eosinophils, IL-5, IL-6, and macrophage inflammatory protein 1β after the second allergen challenge. By contrast, the IL-13 levels were higher and eotaxin levels first increased after repetitive allergen challenge. There was no correlation between total nasal symptom score and elevated cell or cytokine levels. Nasal nitric oxide levels were nonspecifically elevated in both patients with allergy and healthy controls. Conclusion A subset of cellular and soluble biomarkers in nasal lavage and secretion reveals specificity and reproducibility in patients with allergic rhinitis. These can be used to measure the immunologic efficacy of antiallergic treatments in an allergen challenge chamber. Carryover effects attributable to priming must be considered when designing cross-over studies. 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Müller, Meike, PhD ; Koch, Wolfgang, PhD ; Hohlfeld, Jens M., MD ; Krug, Norbert, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-3776f174c7533b420b5fe21abfeedb097a6c8a212afb4e997bf67f5940e521473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Allergens - immunology</topic><topic>Allergy and Immunology</topic><topic>Biomarkers</topic><topic>Case-Control Studies</topic><topic>Cytokines - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Immunization</topic><topic>Inflammation Mediators - metabolism</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Nasal Lavage Fluid - immunology</topic><topic>Nasal Mucosa - immunology</topic><topic>Nasal Mucosa - metabolism</topic><topic>Nasal Provocation Tests</topic><topic>Nitric Oxide - metabolism</topic><topic>Pilot Projects</topic><topic>Pollen - immunology</topic><topic>Rhinitis, Allergic - diagnosis</topic><topic>Rhinitis, Allergic - immunology</topic><topic>Rhinitis, Allergic - metabolism</topic><topic>Rhinomanometry</topic><topic>Severity of Illness Index</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Badorrek, Philipp, MD</creatorcontrib><creatorcontrib>Müller, Meike, PhD</creatorcontrib><creatorcontrib>Koch, Wolfgang, PhD</creatorcontrib><creatorcontrib>Hohlfeld, Jens M., MD</creatorcontrib><creatorcontrib>Krug, Norbert, MD</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of allergy, asthma, &amp; immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Badorrek, Philipp, MD</au><au>Müller, Meike, PhD</au><au>Koch, Wolfgang, PhD</au><au>Hohlfeld, Jens M., MD</au><au>Krug, Norbert, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after allergen challenge chamber exposure</atitle><jtitle>Annals of allergy, asthma, &amp; immunology</jtitle><addtitle>Ann Allergy Asthma Immunol</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>118</volume><issue>3</issue><spage>290</spage><epage>297</epage><pages>290-297</pages><issn>1081-1206</issn><eissn>1534-4436</eissn><abstract>Abstract Background Allergic rhinitis is an inflammatory disease that causes cellular influx and mediator release in the nose. These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments. Objective To assess the specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after grass pollen exposure in an allergen challenge chamber. Methods In a monocenter pilot study, 15 patients with allergic rhinitis and 19 healthy individuals underwent two 4-hour Dactylis glomerate pollen challenges in the challenge chamber with an interval of 21 days. Before challenge, on exit, and after 2 and 22 hours, a nasal lavage was performed and nasal secretions were collected on filter paper to determine a wide panel of cells and mediators. Furthermore, total nasal symptom score, nasal flow, and nasal nitric oxide were measured. Results Pollen exposure significantly increased eosinophil, interleukin (IL) 5, IL-6, IL-13, and macrophage inflammatory protein 1β levels in allergic patients but not in healthy individuals. The effect could be reproduced for eosinophils, IL-5, IL-6, and macrophage inflammatory protein 1β after the second allergen challenge. By contrast, the IL-13 levels were higher and eotaxin levels first increased after repetitive allergen challenge. There was no correlation between total nasal symptom score and elevated cell or cytokine levels. Nasal nitric oxide levels were nonspecifically elevated in both patients with allergy and healthy controls. Conclusion A subset of cellular and soluble biomarkers in nasal lavage and secretion reveals specificity and reproducibility in patients with allergic rhinitis. These can be used to measure the immunologic efficacy of antiallergic treatments in an allergen challenge chamber. Carryover effects attributable to priming must be considered when designing cross-over studies. 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subjects Adult
Allergens - immunology
Allergy and Immunology
Biomarkers
Case-Control Studies
Cytokines - metabolism
Female
Humans
Immunization
Inflammation Mediators - metabolism
Leukocyte Count
Male
Nasal Lavage Fluid - immunology
Nasal Mucosa - immunology
Nasal Mucosa - metabolism
Nasal Provocation Tests
Nitric Oxide - metabolism
Pilot Projects
Pollen - immunology
Rhinitis, Allergic - diagnosis
Rhinitis, Allergic - immunology
Rhinitis, Allergic - metabolism
Rhinomanometry
Severity of Illness Index
Young Adult
title Specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after allergen challenge chamber exposure
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