Artemisia annua-sublingual immunotherapy for seasonal allergic rhinitis: A randomized controlled trial.


Journal

Allergy
ISSN: 1398-9995
Titre abrégé: Allergy
Pays: Denmark
ID NLM: 7804028

Informations de publication

Date de publication:
08 2020
Historique:
received: 11 08 2019
revised: 17 11 2019
accepted: 08 12 2019
pubmed: 8 2 2020
medline: 15 5 2021
entrez: 8 2 2020
Statut: ppublish

Résumé

Artemisia annua is an important autumnal pollen allergen for seasonal allergic rhinitis (SAR) in northern China. To date, no study has investigated allergen immunotherapy with A annua. We aimed to investigate the efficacy and mechanisms underlying A annua-sublingual immunotherapy (SLIT). This was a randomized, double-blind, placebo-controlled phase III clinical trial involving 71 SAR patients, randomized to SLIT with A annua extract (n = 47) or placebo (n = 24) for 32 weeks. Total nasal symptom score (TNSS; primary clinical end point) was evaluated at baseline (peak pollen phase (PPP) in the previous year), initiation of A annua-SLIT, 1st PPP during SLIT, end of SLIT and 2nd PPP during follow-up. Blood samples and nasal secretions were collected at beginning and after SLIT for assessment of T cells and inflammatory mediators. Safety was assessed according to adverse events (AEs) reported. Artemisia annua-SLIT significantly reduced TNSS to a greater level from baseline (from 9.45 ± 1.68 to 6.16 ± 2.27) than placebo (from 9.29 ± 2.09 to 9.05 ± 2.40) at the 1st PPP (P < .001) and sustained the improvement in symptoms throughout to the 2nd PPP. Preseasonal A annua-SLIT for 16 weeks significantly decreased Th2 cells, increased nTreg and Tr1 cells in blood; and increased cystatin 1 (CST1) in nasal secretion after 16 and 32 weeks compared with pretreatment. Overall, 17/47 patients experienced mild local AEs and 2 patients mild systemic AEs, after A annua-SLIT. Artemisia annua-SLIT is an efficacious and safe treatment in patients with A annua SAR.

Sections du résumé

BACKGROUND
Artemisia annua is an important autumnal pollen allergen for seasonal allergic rhinitis (SAR) in northern China. To date, no study has investigated allergen immunotherapy with A annua. We aimed to investigate the efficacy and mechanisms underlying A annua-sublingual immunotherapy (SLIT).
METHODS
This was a randomized, double-blind, placebo-controlled phase III clinical trial involving 71 SAR patients, randomized to SLIT with A annua extract (n = 47) or placebo (n = 24) for 32 weeks. Total nasal symptom score (TNSS; primary clinical end point) was evaluated at baseline (peak pollen phase (PPP) in the previous year), initiation of A annua-SLIT, 1st PPP during SLIT, end of SLIT and 2nd PPP during follow-up. Blood samples and nasal secretions were collected at beginning and after SLIT for assessment of T cells and inflammatory mediators. Safety was assessed according to adverse events (AEs) reported.
RESULTS
Artemisia annua-SLIT significantly reduced TNSS to a greater level from baseline (from 9.45 ± 1.68 to 6.16 ± 2.27) than placebo (from 9.29 ± 2.09 to 9.05 ± 2.40) at the 1st PPP (P < .001) and sustained the improvement in symptoms throughout to the 2nd PPP. Preseasonal A annua-SLIT for 16 weeks significantly decreased Th2 cells, increased nTreg and Tr1 cells in blood; and increased cystatin 1 (CST1) in nasal secretion after 16 and 32 weeks compared with pretreatment. Overall, 17/47 patients experienced mild local AEs and 2 patients mild systemic AEs, after A annua-SLIT.
CONCLUSION
Artemisia annua-SLIT is an efficacious and safe treatment in patients with A annua SAR.

Identifiants

pubmed: 32030780
doi: 10.1111/all.14218
doi:

Substances chimiques

Allergens 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2026-2036

Informations de copyright

© 2020 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.

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Auteurs

Hongfei Lou (H)

Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.

Yanran Huang (Y)

Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.

Yuhui Ouyang (Y)

Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.
Department of Allergy, Beijing TongRen Hospital, Capital Medical University, Beijing, China.

Yuan Zhang (Y)

Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.
Department of Allergy, Beijing TongRen Hospital, Capital Medical University, Beijing, China.

Lin Xi (L)

Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.
Department of Allergy, Beijing TongRen Hospital, Capital Medical University, Beijing, China.

Xiaohan Chu (X)

Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.

Yang Wang (Y)

Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.

Chengshuo Wang (C)

Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.

Luo Zhang (L)

Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.
Department of Allergy, Beijing TongRen Hospital, Capital Medical University, Beijing, China.

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