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Rhinovirus Species-Specific Antibodies Differentially Reflect Clinical Outcomes in Health and Asthma.
Megremis, Spyridon; Niespodziana, Katarzyna; Cabauatan, Clarissa; Xepapadaki, Paraskevi; Kowalski, Marek L; Jartti, Tuomas; Bachert, Claus; Finotto, Susetta; West, Peter; Stamataki, Sofia; Lewandowska-Polak, Anna; Lukkarinen, Heikki; Zhang, Nan; Zimmermann, Theodor; Stolz, Frank; Neubauer, Angela; Akdis, Mübeccel; Andreakos, Evangelos; Valenta, Rudolf; Papadopoulos, Nikolaos G.
Affiliation
  • Megremis S; Division of Infection, Immunity and Respiratory Medicine and.
  • Niespodziana K; Division of Immunopathology, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
  • Cabauatan C; Division of Immunopathology, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
  • Xepapadaki P; Allergy Department, 2nd Pediatric Clinic, National and Kapodistrian University of Athens, Athens, Greece.
  • Kowalski ML; Department of Immunology, Rheumatology and Allergy, Medical University of Lodz, Lodz, Poland.
  • Jartti T; Department of Paediatrics, Turku University Hospital, University of Turku, Turku, Finland.
  • Bachert C; Upper Airways Research Laboratory, Ghent University, Ghent, Belgium.
  • Finotto S; Department of Molecular Pneumology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • West P; Division of Infection, Immunity and Respiratory Medicine and.
  • Stamataki S; Athens General Children's Hospital "Pan & Aglaia Kyriakou," Athens, Greece.
  • Lewandowska-Polak A; Department of Immunology, Rheumatology and Allergy, Medical University of Lodz, Lodz, Poland.
  • Lukkarinen H; Department of Paediatrics, Turku University Hospital, University of Turku, Turku, Finland.
  • Zhang N; Upper Airways Research Laboratory, Ghent University, Ghent, Belgium.
  • Zimmermann T; Department of Molecular Pneumology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Stolz F; Biomay, AG, Vienna, Austria.
  • Neubauer A; Biomay, AG, Vienna, Austria.
  • Akdis M; Swiss Institute of Allergy and Asthma Research, University of Zurich, Zurich, Switzerland.
  • Andreakos E; Biomedical Research Foundation, Academy of Athens, Athens, Greece; and.
  • Valenta R; Division of Immunopathology, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
  • Papadopoulos NG; NRC Institute of Immunology FMBA of Russia, Moscow, Russia.
Am J Respir Crit Care Med ; 198(12): 1490-1499, 2018 12 15.
Article de En | MEDLINE | ID: mdl-30134114
Rationale: Rhinoviruses (RVs) are major triggers of common cold and acute asthma exacerbations. RV species A, B, and C may have distinct clinical impact; however, little is known regarding RV species-specific antibody responses in health and asthma.Objectives: To describe and compare total and RV species-specific antibody levels in healthy children and children with asthma, away from an acute event.Methods: Serum samples from 163 preschool children with mild to moderate asthma and 72 healthy control subjects from the multinational Predicta cohort were analyzed using the recently developed PreDicta RV antibody chip.Measurements and Main Results: RV antibody levels varied, with RV-C and RV-A being higher than RV-B in both groups. Compared with control subjects, asthma was characterized by significantly higher levels of antibodies to RV-A and RV-C, but not RV-B. RV antibody levels positively correlated with the number of common colds over the previous year in healthy children, and wheeze episodes in children with asthma. Antibody levels also positively correlated with asthma severity but not with current asthma control.Conclusions: The variable humoral response to RV species in both groups suggests a differential infectivity pattern between RV species. In healthy preschoolers, RV antibodies accumulate with colds. In asthma, RV-A and RV-C antibodies are much higher and further increase with disease severity and wheeze episodes. Higher antibody levels in asthma may be caused by a compromised innate immune response, leading to increased exposure of the adaptive immune response to the virus. Importantly, there is no apparent protection with increasing levels of antibodies.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Asthme / Rhinovirus / Anticorps antiviraux Type d'étude: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Child, preschool / Humans Langue: En Journal: Am J Respir Crit Care Med Sujet du journal: TERAPIA INTENSIVA Année: 2018 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Asthme / Rhinovirus / Anticorps antiviraux Type d'étude: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Child, preschool / Humans Langue: En Journal: Am J Respir Crit Care Med Sujet du journal: TERAPIA INTENSIVA Année: 2018 Type de document: Article Pays de publication: États-Unis d'Amérique