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Protective Effect of Allergen Immunotherapy in Patients With Allergic Rhinitis and Asthma Against COVID-19 Infection: Observational, Nationwide, and Multicenter Study

医学 哮喘 变应原免疫治疗 过敏 奥马佐单抗 过敏原 内科学 2019年冠状病毒病(COVID-19) 观察研究 免疫学 呼吸道感染 儿科 免疫球蛋白E 呼吸系统 疾病 抗体 传染病(医学专业)
作者
Rundong Qin,Yan Feng,Huanping Zhang,Beibei Zhao,Wei Lei,Hongying Sun,Lili Zhi,Zheng Zhong-sheng,Siqin Wang,Yafeng Yu,S. Jiang,Changshan Liu,Xingkai Ma,Hui Ma,Huiying Wang,Hang Lin,Qiaojie He,Lingying Wu,Yingying Zhai,Huagang Lu,Chen Shi,Yan Ma,Xiaohong Jin,Shan Deng,Nanshan Zhong,Ruchong Chen,Jing Li
出处
期刊:JMIR public health and surveillance [JMIR Publications]
卷期号:10: e50846-e50846
标识
DOI:10.2196/50846
摘要

Abstract Background Allergic diseases are associated with an increased susceptibility to respiratory tract infections. Although allergen immunotherapy (AIT) alters the course of allergies, there is limited evidence from clinical practice demonstrating its ability to enhance the host defense against pathogens. Objective The aim of this study was to investigate the protective effect of AIT against viral infection in patients with allergic rhinitis (AR) and allergic asthma (AS) based on clinical evidence. Methods A multicenter, questionnaire-based survey was conducted during a tremendous surge in COVID-19 cases between February 10, 2023, and March 15, 2023, in 81 centers across China recruiting healthy volunteers and patients with AR and AS to investigate the clinical outcomes of COVID-19 infection. Results Of 10,151 participants recruited in the survey, 3654 patients and 2192 healthy volunteers who tested positive for COVID-19 were included in this analysis after screening. Overall, no significant differences in COVID-19 outcomes were observed between patients and healthy volunteers. An additional 451 patients were excluded due to their use of biologics as the sole add-on treatment, leaving 3203 patients in the further analysis. Of them, 1752 were undergoing routine medication treatment (RMT; the RMT group), whereas 1057 and 394 were receiving AIT and a combination of AIT and omalizumab (OMA) as adjunct therapies to RMT, respectively (AIT+RMT and AIT+OMA+RMT groups). The AIT group showed milder COVID-19 symptoms, shorter recovery periods, and a lower likelihood of hospitalization or emergency department visits than the RMT group (all P <.05). After adjusting for confounding factors, including demographic characteristics and COVID-19 vaccination, AIT remained a significant protective factor associated with shorter recovery time (adjusted odds ratio [OR] 0.62, 95% CI 0.52‐0.75; adjusted P <.001) and a lower incidence of hospitalization or emergency department visits (adjusted OR 0.73, 95% CI 0.54‐0.98; adjusted P =.03). Furthermore, the AIT+OMA+RMT group showed greater protection with a shorter recovery time (adjusted OR 0.51, 95% CI 0.34‐0.74; adjusted P <.001) than the AIT+RMT group. Conclusions Our multicenter observational study provides valuable clinical evidence supporting the protective effect of AIT against COVID-19 infection in patients with AR and AS.

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