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自身免疫背景下的变应原免疫疗法:一项病例研究。

Allergen Immunotherapy in Autoimmune Terrain: A Case Study.

作者信息

Samajdar Shambo S, Moitra Saibal, Mukherjee Shatavisa, Pal Jyotirmoy, Joshi Shashank R

机构信息

Diabetes and Allergy-Asthma Therapeutics Specialty Clinic, Kolkata, India.

Allergy Asthma Treatment Centre, Kolkata, India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2025 Jan;77(1):528-531. doi: 10.1007/s12070-024-05164-y. Epub 2024 Oct 28.

Abstract

Allergen immunotherapy (AIT), or specific immunotherapy (SIT), is an effective treatment for inducing immune tolerance to specific allergens. It is widely used for allergic rhinitis, conjunctivitis, asthma, and Hymenoptera venom allergies, with recent applications to food allergies and atopic dermatitis. Despite its benefits, the use of SIT in patients with autoimmune diseases is controversial due to concerns about its potential to induce or exacerbate autoimmune conditions. This report examines a case of autoimmune hypothyroidism developing during AIT and the management decisions involved. A 26-year-old female with a history of moderate to severe persistent allergic rhinitis and childhood asthma presented with severe malaise, weakness, and fatigue over the past three months. She had a family history of asthma and allergic rhinitis. The patient had been on AIT for six months and was using intranasal fluticasone furoate nasal spray daily. Initial laboratory investigations prior to AIT showed normal thyroid function. Three months into AIT, she developed hypothyroidism, confirmed by elevated TSH levels and positive anti-TPO antibodies. A causality assessment suggested a "possible" link between AIT and hypothyroidism. However, a risk-benefit analysis favored the continuation of AIT along with the initiation of L-thyroxine therapy. After six months of thyroid hormone replacement, her TSH levels normalized, and her allergic rhinitis symptoms significantly improved. This case underscores the complexity of managing coexisting allergic and autoimmune conditions. The decision to continue AIT, despite the onset of hypothyroidism, was based on a thorough risk-benefit analysis, emphasizing the need for personalized treatment plans. Understanding the immunological mechanisms, particularly the balance between Th17 and Treg cells, is crucial. Neutrophils play a significant role as both effectors and modulators of immune responses. The clinical pharmacologist's recommendation was informed by these factors and the manageable nature of hypothyroidism with hormone replacement therapy. The continuation of AIT was justified by its benefits in managing allergic rhinitis and the manageable nature of hypothyroidism with hormone therapy. This case highlights the importance of personalized medicine and continuous monitoring in treatment decisions for patients with coexisting conditions.

摘要

变应原免疫疗法(AIT),即特异性免疫疗法(SIT),是诱导对特定变应原产生免疫耐受的一种有效治疗方法。它广泛用于治疗变应性鼻炎、结膜炎、哮喘和膜翅目昆虫毒液过敏,最近也应用于食物过敏和特应性皮炎。尽管有诸多益处,但由于担心其可能诱发或加重自身免疫性疾病,SIT在自身免疫性疾病患者中的应用仍存在争议。本报告探讨了1例在AIT期间发生自身免疫性甲状腺功能减退的病例及相关管理决策。一名26岁女性,有中度至重度持续性变应性鼻炎病史及儿童期哮喘病史,在过去三个月出现严重不适、乏力和疲劳。她有哮喘和变应性鼻炎家族史。该患者接受AIT已6个月,且每天使用糠酸氟替卡松鼻喷雾剂。AIT前的初始实验室检查显示甲状腺功能正常。AIT进行3个月后,她出现甲状腺功能减退,促甲状腺激素(TSH)水平升高及抗甲状腺过氧化物酶(anti-TPO)抗体阳性证实了这一点。因果关系评估表明AIT与甲状腺功能减退之间存在“可能”的联系。然而,风险效益分析支持继续进行AIT并开始左甲状腺素治疗。经过6个月的甲状腺激素替代治疗,她的TSH水平恢复正常,变应性鼻炎症状明显改善。该病例强调了同时管理变应性和自身免疫性疾病的复杂性。尽管出现了甲状腺功能减退,但继续进行AIT的决定是基于全面的风险效益分析,强调了个性化治疗方案的必要性。了解免疫机制,尤其是辅助性T细胞17(Th17)和调节性T细胞(Treg)之间的平衡至关重要。中性粒细胞作为免疫反应的效应细胞和调节细胞均发挥重要作用。这些因素以及甲状腺功能减退通过激素替代疗法易于控制的特性为临床药理学家的建议提供了依据。AIT在治疗变应性鼻炎方面的益处以及甲状腺功能减退通过激素治疗易于控制的特性证明了继续进行AIT是合理的。该病例突出了个性化医疗以及对合并疾病患者治疗决策进行持续监测的重要性。

相似文献

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Allergen Immunotherapy in Autoimmune Terrain: A Case Study.自身免疫背景下的变应原免疫疗法:一项病例研究。
Indian J Otolaryngol Head Neck Surg. 2025 Jan;77(1):528-531. doi: 10.1007/s12070-024-05164-y. Epub 2024 Oct 28.
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本文引用的文献

1
Clinical Practice Guideline: Immunotherapy for Inhalant Allergy.临床实践指南:变应原吸入性免疫疗法。
Otolaryngol Head Neck Surg. 2024 Mar;170 Suppl 1(Suppl 1):S1-S42. doi: 10.1002/ohn.648.
8
Allergen-specific immunotherapy and risk of autoimmune disease.变应原特异性免疫疗法与自身免疫性疾病风险。
Curr Opin Allergy Clin Immunol. 2012 Dec;12(6):635-9. doi: 10.1097/ACI.0b013e3283588c8d.

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