Clinical outcomes of 2-year Artemisia annua sublingual immunotherapy in allergic rhinoconjunctivitis children and adult patients.

IF 2.1 Q3 ALLERGY
Asia Pacific Allergy Pub Date : 2026-04-01 Epub Date: 2025-10-06 DOI:10.5415/apallergy.0000000000000231
Change Fan, Huijiao Cai, Xin Tong, Tingting Ma, Yanfei Li, Liya Ai, Xueyan Wang
{"title":"Clinical outcomes of 2-year <i>Artemisia annua</i> sublingual immunotherapy in allergic rhinoconjunctivitis children and adult patients.","authors":"Change Fan, Huijiao Cai, Xin Tong, Tingting Ma, Yanfei Li, Liya Ai, Xueyan Wang","doi":"10.5415/apallergy.0000000000000231","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Pollen immunotherapy has increasingly gained attention in China. However, the majority of existing research is limited to evaluating therapeutic effects within a 1-year treatment period, with insufficient evidence regarding the longer-term course of treatment.</p><p><strong>Objectives: </strong>Our study was designed to evaluate the clinical effectiveness and safety of 2-year <i>Artemisia annua</i> sublingual immunotherapy (SLIT) treatment in allergic rhinoconjunctivitis (ARC) patients of all ages.</p><p><strong>Methods: </strong>This study was conducted as a nonblind randomized controlled trial. Fifty eligible patients (7-57 years old) sensitized to <i>Artemisia</i> pollen were randomized into SLIT (n = 25) and control groups (n = 25). The SLIT group administered daily <i>Artemisia annua</i> SLIT for 2 years, and the control group only accepted symptomatic medications. Clinical outcomes including total rhinoconjunctivitis symptom score (TRSS), total medication score (TMS), combined scores of medication and rhinoconjunctivitis symptom (CSMRS), and the visual analog scale (VAS) scores were assessed across 3 consecutive pollen seasons (2021 as baseline, followed by 2022 and 2023). Additionally, the occurrence of adverse events (AEs) was used to evaluate its safety.</p><p><strong>Results: </strong>Finally, 43 patients (SLIT: 21, control: 22) completed this study. When compared with the control group, the patients in SLIT group exhibited remarkable improvements in TRSS, TMS, CSMRS, and VAS scores during the 2023 pollen season (<i>P</i> < 0.001). Especially, more patients in the SLIT group showed greater improvement in symptoms, medication use, and the overall situation. Notably, no severe AEs were reported throughout the whole study.</p><p><strong>Conclusions: </strong>Two years of <i>Artemisia annua</i> SLIT treatment was effective and well-tolerated in patients with ARC, confirmed by their improved symptoms and reduced medication use.</p>","PeriodicalId":8488,"journal":{"name":"Asia Pacific Allergy","volume":"16 2","pages":"92-99"},"PeriodicalIF":2.1000,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13060872/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asia Pacific Allergy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5415/apallergy.0000000000000231","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/6 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Pollen immunotherapy has increasingly gained attention in China. However, the majority of existing research is limited to evaluating therapeutic effects within a 1-year treatment period, with insufficient evidence regarding the longer-term course of treatment.

Objectives: Our study was designed to evaluate the clinical effectiveness and safety of 2-year Artemisia annua sublingual immunotherapy (SLIT) treatment in allergic rhinoconjunctivitis (ARC) patients of all ages.

Methods: This study was conducted as a nonblind randomized controlled trial. Fifty eligible patients (7-57 years old) sensitized to Artemisia pollen were randomized into SLIT (n = 25) and control groups (n = 25). The SLIT group administered daily Artemisia annua SLIT for 2 years, and the control group only accepted symptomatic medications. Clinical outcomes including total rhinoconjunctivitis symptom score (TRSS), total medication score (TMS), combined scores of medication and rhinoconjunctivitis symptom (CSMRS), and the visual analog scale (VAS) scores were assessed across 3 consecutive pollen seasons (2021 as baseline, followed by 2022 and 2023). Additionally, the occurrence of adverse events (AEs) was used to evaluate its safety.

Results: Finally, 43 patients (SLIT: 21, control: 22) completed this study. When compared with the control group, the patients in SLIT group exhibited remarkable improvements in TRSS, TMS, CSMRS, and VAS scores during the 2023 pollen season (P < 0.001). Especially, more patients in the SLIT group showed greater improvement in symptoms, medication use, and the overall situation. Notably, no severe AEs were reported throughout the whole study.

Conclusions: Two years of Artemisia annua SLIT treatment was effective and well-tolerated in patients with ARC, confirmed by their improved symptoms and reduced medication use.

2年青蒿舌下免疫治疗儿童和成人变应性鼻结膜炎的临床疗效。
背景:花粉免疫疗法在中国越来越受到关注。然而,现有的大多数研究仅限于评估1年治疗期内的治疗效果,关于长期治疗过程的证据不足。目的:本研究旨在评价2年青蒿舌下免疫疗法(SLIT)治疗所有年龄段变应性鼻结膜炎(ARC)患者的临床疗效和安全性。方法:采用非盲随机对照试验。50例符合条件的青蒿花粉致敏患者(7 ~ 57岁)随机分为SLIT组(n = 25)和对照组(n = 25)。SLIT组每日给予青蒿SLIT治疗2年,对照组仅接受对症药物治疗。临床结果包括鼻结膜炎症状总评分(TRSS)、药物总评分(TMS)、药物和鼻结膜炎症状联合评分(CSMRS)和视觉模拟量表(VAS)评分,连续3个花粉季节(2021年为基线,随后是2022年和2023年)进行评估。此外,用不良事件(ae)发生率来评价其安全性。结果:最终,43例患者(狭缝组21例,对照组22例)完成了本研究。与对照组相比,SLIT组患者在2023年花粉季节的TRSS、TMS、CSMRS和VAS评分均有显著改善(P < 0.001)。特别是,SLIT组中更多的患者在症状、药物使用和整体情况方面表现出更大的改善。值得注意的是,在整个研究中没有报道严重的不良反应。结论:两年的青蒿SLIT治疗对ARC患者有效且耐受性良好,其症状改善和用药减少证实了这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.50
自引率
5.90%
发文量
33
期刊介绍: Asia Pacific Allergy (AP Allergy) is the official journal of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI). Although the primary aim of the journal is to promote communication between Asia Pacific scientists who are interested in allergy, asthma, and clinical immunology including immunodeficiency, the journal is intended to be available worldwide. To enable scientists and clinicians from emerging societies appreciate the scope and intent of the journal, early issues will contain more educational review material. For better communication and understanding, it will include rational concepts related to the diagnosis and management of asthma and other immunological conditions. Over time, the journal will increase the number of original research papers to become the foremost citation journal for allergy and clinical immunology information of the Asia Pacific in the future.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书