Efficacy of immunoglobulin replacement therapy and azithromycin in severe asthma with antibody deficiency.


Journal

Allergology international : official journal of the Japanese Society of Allergology
ISSN: 1440-1592
Titre abrégé: Allergol Int
Pays: England
ID NLM: 9616296

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 19 06 2019
revised: 25 10 2019
accepted: 30 10 2019
pubmed: 10 12 2019
medline: 15 12 2020
entrez: 9 12 2019
Statut: ppublish

Résumé

Although antibody deficiency (AD) is a well-known cause of recurrent respiratory infections, there are few data on its impact in adults with asthma. The objective of the present study was to assess outcomes in adults with severe asthma and AD after treatment with either azithromycin or subcutaneous immunoglobulins (SCIg). We performed a 5-year, prospective, observational, two-centre study of adults with severe asthma and AD in France. Bronchiectasis was ruled out by high-resolution computed tomography. Patients were treated for one year with either azithromycin (250 mg every other day) or SCIg (0.4-0.6 g/kg/months, weekly). All patients were evaluated for exacerbations, asthma control and lung function at baseline and then one year after treatment initiation. Thirty-nine patients with severe asthma were included in the study: 14 had been treated with azithromycin and 25 had been treated with SCIg. Before the initiation of treatment for AD, all patients had an Asthma Control Questionnaire (ACQ-7) score > 1.5 (mean ± SD: 2.71 ± 0.53) despite treatment at GINA step 4 or 5, and had a high exacerbation rate requiring oral corticosteroids and/or rescue antibiotics (∼7.2 ± 2.1/patient/year). One year after treatment initiation, we observed a significantly higher FEV1 (mean: 0.18 ± 0.22 L) and ACQ-7 score (1.26 ± 0.68), and a significantly lower exacerbation rate (1.63 ± 1.24/patient/year). Treatment of AD dramatically improved asthma outcomes - suggesting that adults with severe asthma and recurrent respiratory infections should be screened and (if appropriate) treated for AD.

Sections du résumé

BACKGROUND BACKGROUND
Although antibody deficiency (AD) is a well-known cause of recurrent respiratory infections, there are few data on its impact in adults with asthma. The objective of the present study was to assess outcomes in adults with severe asthma and AD after treatment with either azithromycin or subcutaneous immunoglobulins (SCIg).
METHODS METHODS
We performed a 5-year, prospective, observational, two-centre study of adults with severe asthma and AD in France. Bronchiectasis was ruled out by high-resolution computed tomography. Patients were treated for one year with either azithromycin (250 mg every other day) or SCIg (0.4-0.6 g/kg/months, weekly). All patients were evaluated for exacerbations, asthma control and lung function at baseline and then one year after treatment initiation.
RESULTS RESULTS
Thirty-nine patients with severe asthma were included in the study: 14 had been treated with azithromycin and 25 had been treated with SCIg. Before the initiation of treatment for AD, all patients had an Asthma Control Questionnaire (ACQ-7) score > 1.5 (mean ± SD: 2.71 ± 0.53) despite treatment at GINA step 4 or 5, and had a high exacerbation rate requiring oral corticosteroids and/or rescue antibiotics (∼7.2 ± 2.1/patient/year). One year after treatment initiation, we observed a significantly higher FEV1 (mean: 0.18 ± 0.22 L) and ACQ-7 score (1.26 ± 0.68), and a significantly lower exacerbation rate (1.63 ± 1.24/patient/year).
CONCLUSIONS CONCLUSIONS
Treatment of AD dramatically improved asthma outcomes - suggesting that adults with severe asthma and recurrent respiratory infections should be screened and (if appropriate) treated for AD.

Identifiants

pubmed: 31812484
pii: S1323-8930(19)30175-3
doi: 10.1016/j.alit.2019.10.011
pii:
doi:

Substances chimiques

Immunoglobulins 0
Azithromycin 83905-01-5

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

215-222

Informations de copyright

Copyright © 2019 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved.

Auteurs

Angelica Tiotiu (A)

Department of Pulmonology, Nancy University Hospital, Nancy, France; Development, Adaptation and Disadvantage, Cardio-Respiratory Regulations and Motor Control, University of Lorraine, Nancy, France; National Heart and Lung Institute, Airway Disease Section, Imperial College London, London, UK. Electronic address: angelica.tiotiu@yahoo.com.

Hélène Salvator (H)

Department of Airway Diseases, Foch Hospital, Suresnes, France; Foch Hospital, Paris Saclay University, Suresnes, France.

Roland Jaussaud (R)

Department of Internal Medicine, Nancy University Hospital, Nancy, France; Faculty of Medicine, University of Lorraine, Nancy, France.

Roger Jankowski (R)

Faculty of Medicine, University of Lorraine, Nancy, France; ENT Department, Nancy University Hospital, Nancy, France.

Louis-Jean Couderc (LJ)

Department of Airway Diseases, Foch Hospital, Suresnes, France; Foch Hospital, Paris Saclay University, Suresnes, France.

Emilie Catherinot (E)

Department of Airway Diseases, Foch Hospital, Suresnes, France.

Philippe Devillier (P)

Department of Airway Diseases, Foch Hospital, Suresnes, France; Foch Hospital, Paris Saclay University, Suresnes, France.

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Classifications MeSH