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Anti-IL-5 in Mild Asthma Alters Rhinovirus-induced Macrophage, B-Cell, and Neutrophil Responses (MATERIAL). A Placebo-controlled, Double-Blind Study.
Sabogal Piñeros, Yanaika S; Bal, Suzanne M; van de Pol, Marianne A; Dierdorp, Barbara S; Dekker, Tamara; Dijkhuis, Annemiek; Brinkman, Paul; van der Sluijs, Koen F; Zwinderman, Aeilko H; Majoor, Christof J; Bonta, Peter I; Ravanetti, Lara; Sterk, Peter J; Lutter, René.
Afiliación
  • Sabogal Piñeros YS; 1 Department of Respiratory Medicine.
  • Bal SM; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • van de Pol MA; 1 Department of Respiratory Medicine.
  • Dierdorp BS; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • Dekker T; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • Dijkhuis A; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • Brinkman P; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • van der Sluijs KF; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • Zwinderman AH; 1 Department of Respiratory Medicine.
  • Majoor CJ; 2 Department of Experimental Immunology (Amsterdam Infection & Immunity Institute), and.
  • Bonta PI; 3 Department of Clinical Epidemiology, Bioinformatics, and Biostatistics, University of Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Ravanetti L; 1 Department of Respiratory Medicine.
  • Sterk PJ; 1 Department of Respiratory Medicine.
  • Lutter R; 1 Department of Respiratory Medicine.
Am J Respir Crit Care Med ; 199(4): 508-517, 2019 02 15.
Article en En | MEDLINE | ID: mdl-30192638
ABSTRACT
RATIONALE Eosinophils drive pathophysiology in stable and exacerbating eosinophilic asthma, and therefore treatment is focused on the reduction of eosinophil numbers. Mepolizumab, a humanized monoclonal antibody that neutralizes IL-5 and efficiently attenuates eosinophils, proved clinically effective in severe eosinophilic asthma but not in mild asthma.

OBJECTIVES:

To study the effect of mepolizumab on virus-induced immune responses in mild asthma.

METHODS:

Patients with mild asthma, steroid-naive and randomized for eosinophil numbers, received 750 mg mepolizumab intravenously in a placebo-controlled double-blind trial, 2 weeks after which patients were challenged with rhinovirus (RV) 16. FEV1, FVC, fractional exhaled nitric oxide, symptom scores (asthma control score), viral load (PCR), eosinophil numbers, humoral (luminex, ELISA), and cellular (flow cytometry) immune parameters in blood, BAL fluid, and sputum, before and after mepolizumab and RV16, were assessed. MEASUREMENTS AND MAIN

RESULTS:

Mepolizumab attenuated baseline blood eosinophils and their activation, attenuated trendwise sputum eosinophils, and enhanced circulating natural killer cells. Mepolizumab did not affect FEV1, FVC, and fractional exhaled nitric oxide, neither at baseline nor after RV16. On RV16 challenge mepolizumab did not prevent eosinophil activation but did enhance local B lymphocytes and macrophages and reduce neutrophils and their activation. Mepolizumab also enhanced secretory IgA and reduced tryptase in BAL fluid. Finally, mepolizumab affected particularly RV16-induced macrophage inflammatory protein-3a, vascular endothelial growth factor-A, and IL-1RA production in BAL fluid.

CONCLUSIONS:

Mepolizumab failed to prevent activation of remaining eosinophils and changed RV16-induced immune responses in mild asthma. Although these latter effects likely are caused by attenuated eosinophil numbers, we cannot exclude a role for basophils. Clinical trial registered with www.clinicaltrials.gov (NCT 01520051).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asma / Rhinovirus / Linfocitos B / Infecciones por Picornaviridae / Antiasmáticos / Anticuerpos Monoclonales Humanizados / Macrófagos / Neutrófilos Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asma / Rhinovirus / Linfocitos B / Infecciones por Picornaviridae / Antiasmáticos / Anticuerpos Monoclonales Humanizados / Macrófagos / Neutrófilos Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2019 Tipo del documento: Article