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Department of Sense Organs, Sapienza University, Rome, Italy.
Acta Biomed. 2023 Aug 3;94(4):e2023172. doi: 10.23750/abm.v94i4.14239.
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.
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.
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.
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。
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。
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。