Limosilactobacillus reuteri DSM-17938 for preventing cough in adults with mild allergic asthma: A double-blind randomized placebo-controlled cross-over study.


Journal

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
ISSN: 1365-2222
Titre abrégé: Clin Exp Allergy
Pays: England
ID NLM: 8906443

Informations de publication

Date de publication:
09 2021
Historique:
received: 05 05 2021
accepted: 27 06 2021
pubmed: 1 7 2021
medline: 24 3 2022
entrez: 30 6 2021
Statut: ppublish

Résumé

Cough is a common troublesome symptom in asthma which is neuronally mediated. Limosilactobacillus reuteri DSM-17938 (L. reuteri DSM-17938) is a probiotic shown to be effective in pre-clinical models at suppressing neuronal responses to capsaicin, a transient receptor potential vanilloid agonist (TRPV1). Investigate the effects of DSM-17938 versus matched placebo on capsaicin-evoked coughs in mild allergic asthmatics. We performed a 4-visit, randomized, double-blind, placebo-controlled, two-way cross-over study comparing full dose cough responses with inhaled capsaicin in mild allergic asthmatics after 1 month of treatment with DSM-17938 compared with matched placebo. Randomization and allocation to trial group were carried out by a central computer system. Histamine skin prick testing, airway hyper-responsiveness and inflammatory cells in induced sputum were measured at every visit. Blood was collected to extract PBMCs and stimulated with CD3/CD28 to ascertain the effects of DSM-17938 /placebo on T-cell cytokine responses. Seventeen subjects were recruited and 15 completed the study (8 females, mean age 27.3 years). There was no difference in the change in maximum capsaicin-evoked coughs (Emax) after treatment with L. reuteri DSM-17938 compared with placebo [mean difference 2.07 coughs (95% CI -2.77 to 6.91, p = .38) or relative changes in geometric mean ratios for the dose evoking at least half the Emax (ED50) [1.05 (95% CI 0.31-3.58, p = .94)], concentration evoking 2 coughs (C2) [0.63 (0.26-1.53), p = .28] and 5 coughs (C5) [0.79 (0.25-2.50), p = .67]. There was no effect on histamine skin prick wheal size, intensity of itch sensation, methacholine PC20, airway inflammation or T-cell responses after stimulation with CD3/CD28. There were no serious adverse events. One subject developed a mild upper respiratory tract infection and another mild transient nausea whilst on DSM-17938. In this small study in adults with mild allergic asthma, we found no evidence that L. reuteri DSM-17938 has any systemic effects on airway nerves, smooth muscle, sputum inflammatory cells, skin responses or T-cell responses after oral consumption. Clinicaltrials.gov Identifier: NCT03603522.

Sections du résumé

BACKGROUND
Cough is a common troublesome symptom in asthma which is neuronally mediated. Limosilactobacillus reuteri DSM-17938 (L. reuteri DSM-17938) is a probiotic shown to be effective in pre-clinical models at suppressing neuronal responses to capsaicin, a transient receptor potential vanilloid agonist (TRPV1).
OBJECTIVE
Investigate the effects of DSM-17938 versus matched placebo on capsaicin-evoked coughs in mild allergic asthmatics.
METHODS
We performed a 4-visit, randomized, double-blind, placebo-controlled, two-way cross-over study comparing full dose cough responses with inhaled capsaicin in mild allergic asthmatics after 1 month of treatment with DSM-17938 compared with matched placebo. Randomization and allocation to trial group were carried out by a central computer system. Histamine skin prick testing, airway hyper-responsiveness and inflammatory cells in induced sputum were measured at every visit. Blood was collected to extract PBMCs and stimulated with CD3/CD28 to ascertain the effects of DSM-17938 /placebo on T-cell cytokine responses.
RESULTS
Seventeen subjects were recruited and 15 completed the study (8 females, mean age 27.3 years). There was no difference in the change in maximum capsaicin-evoked coughs (Emax) after treatment with L. reuteri DSM-17938 compared with placebo [mean difference 2.07 coughs (95% CI -2.77 to 6.91, p = .38) or relative changes in geometric mean ratios for the dose evoking at least half the Emax (ED50) [1.05 (95% CI 0.31-3.58, p = .94)], concentration evoking 2 coughs (C2) [0.63 (0.26-1.53), p = .28] and 5 coughs (C5) [0.79 (0.25-2.50), p = .67]. There was no effect on histamine skin prick wheal size, intensity of itch sensation, methacholine PC20, airway inflammation or T-cell responses after stimulation with CD3/CD28. There were no serious adverse events. One subject developed a mild upper respiratory tract infection and another mild transient nausea whilst on DSM-17938.
CONCLUSION
In this small study in adults with mild allergic asthma, we found no evidence that L. reuteri DSM-17938 has any systemic effects on airway nerves, smooth muscle, sputum inflammatory cells, skin responses or T-cell responses after oral consumption.
TRIAL REGISTRATION
Clinicaltrials.gov Identifier: NCT03603522.

Identifiants

pubmed: 34192396
doi: 10.1111/cea.13976
doi:

Banques de données

ClinicalTrials.gov
['NCT03603522']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1133-1143

Subventions

Organisme : BioGaia (Sweden)

Informations de copyright

© 2021 John Wiley & Sons Ltd.

Références

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Auteurs

Imran Satia (I)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Firestone Institute for Respiratory Health, St Joseph's Healthcare, Hamilton, ON, Canada.

Ruth Cusack (R)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Catie Stevens (C)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Abbey Schlatman (A)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Jennifer Wattie (J)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Firoz Mian (F)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Kieran J Killian (KJ)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Paul M O'Byrne (PM)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Firestone Institute for Respiratory Health, St Joseph's Healthcare, Hamilton, ON, Canada.

John Bienenstock (J)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Paul Forsythe (P)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Gail M Gauvreau (GM)

Division of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

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