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ORIGINAL RESEARCH article

Front. Allergy

Sec. Asthma

Real-world retrospective study on the efficacy and safety of anti-IgE therapy combined with rush immunotherapy in allergic asthma

Provisionally accepted
Wenchao  ZhangWenchao ZhangDan  LiuDan LiuWenjin  DuWenjin DuZhaoji  MengZhaoji MengXianghua  LinXianghua LinWeili  GuoWeili GuoYuanxi  JinYuanxi JinSiqin  WangSiqin Wang*Qiuxing  ZhangQiuxing Zhang*
  • Henan Provincial People's Hospital, Zhengzhou, China

The final, formatted version of the article will be published soon.

Background:Research on the combination of biologics with rush immunotherapy(RIT) remains scarce, particularly regarding safety and efficacy data in pediatric and hypersensitive populations undergoing rapid desensitization or concurrent biologic therapy. Furthermore, regarding RIT, it remains unclear which patients can effectively reduce the occurrence of adverse reactions when combined with biologics, and which patients fail to achieve such a reduction with this combination therapy. Methods:This retrospective study analyzed 202 patients with mite-induced allergic asthma (2018–2024) receiving RIT alone(n=133) or omalizumab-pretreated RIT (RIT+Omb-pre,n=69). Stratified analyses were conducted based on age, mite sIgE levels, total IgE(T-IgE) levels, and sIgE to T-IgE ratios. Outcomes included systemic adverse reaction(SR) rates, RIT completion rates, improvements in clinical parameters following omalizumab intervention, and 1-year follow-up efficacy across subgroups. Results: Both regimens were well tolerated, with no grade≥3 SRs observed. Compared to RIT alone, RIT+Omb-pre significantly reduced SR incidence (p<0.05) and showed a trend toward higher target peak concentration completion rates (p=0.054). Age-stratified analysis revealed higher SR risks in children/teenager patients versus adults. Subgroup analyses further demonstrated that SR incidence correlated positively with mite sIgE levels and sIgE/T-IgE ratio (p<0.05), but not with T-IgE. Patients with low-risk biomarkers (sIgE grades 1-2 and sIgE/T-IgE <10%) exhibited minimal SR incidence unaffected by omalizumab, whereas high-risk subgroups (sIgE grades 3-6 and sIgE/T-IgE ≥10%) showed significantly elevated SR incidence, which was markedly mitigated by omalizumab (p<0.05).Subgroup with sIgE/T-IgE ratios >16% achieved substantially greater improvements in ACQ scores and daily medication burden compared to those with ratios <16% during the 12-month intervention. Furthermore, this study reaffirmed the age-dependent efficacy correlation, with pediatric patients demonstrating superior therapeutic outcomes to adult patients. Conclusions: Regarding the safety of dust mite rush immunotherapy for allergic asthma, Omalizumab significantly reduces the incidence of SRs in high-risk populations (sIgE grades 3-6 and sIgE/T-IgE ≥10%), whereas it demonstrates limited efficacy in low-risk subgroups(sIgE grades 1-2 and sIgE/T-IgE<10%).

Keywords: Rush immunotherapy, Omalizumab, Mite allergen, Allergic Asthma, Safety

Received: 02 Oct 2025; Accepted: 26 Nov 2025.

Copyright: © 2025 Zhang, Liu, Du, Meng, Lin, Guo, Jin, Wang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Siqin Wang
Qiuxing Zhang

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