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Long-term outcome of omalizumab-assisted desensitisation to cow's milk and eggs in patients refractory to conventional oral immunotherapy: real-life study.奥马珠单抗辅助脱敏治疗对常规口服免疫治疗抵抗的牛奶和鸡蛋过敏患者的长期疗效:真实研究。
Allergol Immunopathol (Madr). 2022 May 1;50(3):1-7. doi: 10.15586/aei.v50i3.537. eCollection 2022.
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Venom Immunotherapy and Aeroallergen Immunotherapy: How Do Their Outcomes Differ?毒液免疫疗法与气传变应原免疫疗法:它们的疗效有何不同?
Front Allergy. 2022 Feb 16;3:854080. doi: 10.3389/falgy.2022.854080. eCollection 2022.
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Worldwide prevalence of rhinitis in adults: A review of definitions and temporal evolution.全球成人鼻炎患病率:定义及时间演变综述
Clin Transl Allergy. 2022 Mar;12(3):e12130. doi: 10.1002/clt2.12130.
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Allergen immunotherapy during the COVID-19 pandemic-A survey of the German Society for Allergy and Clinical Immunology.2019冠状病毒病大流行期间的变应原免疫治疗——德国变态反应和临床免疫学会的一项调查
Clin Transl Allergy. 2022 Mar;12(3):e12134. doi: 10.1002/clt2.12134.
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Combination therapy of specific aeroallergens immunotherapy and omalizumab, in children with severe asthma.特异性气传变应原免疫疗法与奥马珠单抗联合治疗重度哮喘儿童
Allergol Immunopathol (Madr). 2022 Mar 1;50(2):1-6. doi: 10.15586/aei.v50i2.469. eCollection 2022.
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Food allergy across the globe.全球范围内的食物过敏。
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Systemic Allergic Reactions and Anaphylaxis Associated with Allergen Immunotherapy.与变应原免疫治疗相关的全身性过敏反应和过敏反应。
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Allergen Immunotherapy management during vaccinations: An international survey.疫苗接种期间的变应原免疫疗法管理:一项国际调查。
World Allergy Organ J. 2021 Nov;14(11):100601. doi: 10.1016/j.waojou.2021.100601. Epub 2021 Nov 8.
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One hundred and ten years of Allergen Immunotherapy: A journey from empiric observation to evidence.变应原免疫治疗的百年历程:从经验观察到循证医学。
Allergy. 2022 Feb;77(2):454-468. doi: 10.1111/all.15023. Epub 2021 Sep 27.
10
Worldwide surveys on anaphylaxis to sublingual immunotherapy with house dust mite tablets are urgently needed.迫切需要针对屋尘螨片剂舌下免疫疗法过敏反应进行全球调查。
Clin Transl Allergy. 2021 Mar;11(1):e12012. doi: 10.1002/clt2.12012.

皮下变应原免疫治疗的安全性和不良反应:综述。

Safety and adverse reactions in subcutaneous allergen immunotherapy: a review.

机构信息

.

Department of Sense Organs, Sapienza University, Rome, Italy.

出版信息

Acta Biomed. 2023 Aug 3;94(4):e2023172. doi: 10.23750/abm.v94i4.14239.

DOI:10.23750/abm.v94i4.14239
PMID:37539607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10440773/
Abstract

BACKGROUND

Allergen immunotherapy (AIT) is the only treatment which acts on the causes of allergic diseases by modifying their natural history. In the eighties subcutaneous immunotherapy (SCIT) with high biological power allergen extracts caused a number of severe systemic reactions and also fatalities in the UK and the US, resulting in its limitation and in the introduction of other routes of administration. A decisive advance for SCIT safety was understanding that the major cause of mortality was injecting the allergen extract to patients with uncontrolled asthma at the time of injection.

AREAS COVERED

This awareness resulted in a significant decrease in fatalities, but not in their abolition. In 2019, an increase in SCIT-related mortality was observed, suggesting to continue the research for still unidentified factors favoring severe reactions, such as the administration of a wrong extract or of allergen doses higher than listed, unintentional intravenous administration, and missed dose reduction after protracted interruption. Moreover, in the context of the improving of the safety, the role played in tolerance-promoting by adjuvants such as CpG oligodeoxynucleotides has to be taken into account, as well as the potential preventive effect performed by the monoclonal anti-IgE antibody omalizumab against the exacerbation of severe reactions during SCIT.

CONCLUSION

The safety of SCIT is good, but the research to improve it further must continue. In particular, the pathophysiological mechanisms related to AIT for inhalants and for Hymenoptera venom should be studied, based on the evident diversity demonstrated by the complete absence of fatal reactions to Hymenoptera venom immunotherapy from its introduction in comparison with the history of serious and fatal offenses examined in this review.

摘要

背景

变应原免疫治疗(AIT)是唯一通过改变过敏疾病自然进程来针对病因的治疗方法。在 20 世纪 80 年代,高生物效价变应原提取物的皮下免疫治疗(SCIT)在英国和美国引起了许多严重的全身性反应,甚至导致死亡,这导致了其应用受限,并引入了其他给药途径。SCIT 安全性的一个决定性进展是认识到,主要的死亡原因是在注射时给正在接受未控制的哮喘治疗的患者注射变应原提取物。

涵盖领域

这一认识导致死亡率显著下降,但并未完全消除。2019 年,观察到 SCIT 相关死亡率增加,这表明需要继续研究仍未确定的有利于严重反应的因素,例如给予错误的提取物或高于列出的变应原剂量、意外静脉内给药以及在长时间中断后错过剂量减少。此外,在提高安全性的背景下,必须考虑佐剂(如 CpG 寡脱氧核苷酸)在促进耐受中的作用,以及单克隆抗 IgE 抗体奥马珠单抗在 SCIT 期间预防严重反应加重的潜在作用。

结论

SCIT 的安全性良好,但必须继续研究以进一步提高其安全性。特别是,应该根据本综述中检查的严重和致命违规行为的历史,研究吸入性变应原和蜂类毒液的 AIT 相关的病理生理学机制,因为从引入蜂类毒液免疫治疗以来,完全没有致命反应的证据表明存在明显的多样性。