Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
Beijing Key Laboratory of Nasal Disease, Beijing Institute of Otolaryngology, Beijing, China.
Expert Rev Clin Immunol. 2021 Sep;17(9):969-975. doi: 10.1080/1744666X.2021.1968834. Epub 2021 Aug 18.
House dust mite (HDM) is a main perennial allergen causing allergic rhinitis (AR). It has been shown that HDM cross-reacts with a variety of other allergens. Presently, allergen-specific immunotherapy (AIT) is an effective way for management of mono-sensitized HDM AR patients. However, management approaches to polysensitized HDM-sensitized AR patients are not standardized yet.
This article reviews the data available in the literature for cross-reactivity between HDM and inhalant or food allergens, the diagnosis of cross-reactivity in HDM-sensitized AR patients, and the effect of immunotherapy on cross-reactivity in HDM-sensitized AR patients; which may help to develop effective therapeutic strategies for management of polysensitized HDM-sensitized AR patients in the future.
Pan-allergen proteins such as tropomyosin, arginine kinase (AK), glutathione S-transferase (GST), and hemocyanin are responsible for cross-reactivity between HDM and other allergens. To distinguish genuine or cross-reactive sensitization, molecular- or component-resolved diagnosis is suggested to apply in HDM-sensitized AR patients. The effect of HDM immunotherapy to treat the associated cross-reactivity in HDM-sensitized AR patients is still contradictory, and might be dependent on the degree of homology between two allergens. Furthermore, targeting tropomyosin might be a promising way to treat HDM patients with allergen cross-reactivity.
AIT: allergen-specific immunotherapy; AK: arginine kinase; AR: allergic rhinitis; CRD: component-resolved diagnostics; Der f: Dermatophagoides farina; Der p: Dermatophagoides pteronyssinus; EAACI: European Academy of Allergy and Clinical Immunology; GST: glutathione S-transferase; GWAS: genome-wide association study; HDM: house dust mite; IgE: immunoglobulin E; RAST: radioallergosorbent test; sIgE: specific IgE; SIT: specific immunotherapy; SCIT: subcutaneous immunotherapy; SLIT: sublingual immunotherapy; SPT: skin prick test.
屋尘螨(HDM)是引起过敏性鼻炎(AR)的主要常年过敏原。已经表明,HDM 与多种其他过敏原发生交叉反应。目前,过敏原特异性免疫疗法(AIT)是管理单敏 HDM-AR 患者的有效方法。然而,多敏 HDM-敏化 AR 患者的管理方法尚未标准化。
本文综述了文献中关于 HDM 与吸入性或食物过敏原之间交叉反应、HDM 敏化 AR 患者交叉反应的诊断以及 AIT 对 HDM 敏化 AR 患者交叉反应的影响的数据;这可能有助于制定未来多敏 HDM-敏化 AR 患者的有效治疗策略。
原肌球蛋白、精氨酸激酶(AK)、谷胱甘肽 S-转移酶(GST)和血蓝蛋白等泛过敏原蛋白是 HDM 与其他过敏原发生交叉反应的原因。为了区分真正的或交叉反应性致敏,建议在 HDM 敏化 AR 患者中应用分子或成分分辨诊断。HDM 免疫疗法治疗 HDM 敏化 AR 患者相关交叉反应的效果仍然存在争议,可能取决于两种过敏原之间的同源性程度。此外,针对原肌球蛋白可能是治疗具有过敏原交叉反应的 HDM 患者的一种有前途的方法。
AIT:过敏原特异性免疫疗法;AK:精氨酸激酶;AR:过敏性鼻炎;CRD:成分分辨诊断;Der f:屋尘螨;Der p:粉尘螨;EAACI:欧洲过敏与临床免疫学会;GST:谷胱甘肽 S-转移酶;GWAS:全基因组关联研究;HDM:屋尘螨;IgE:免疫球蛋白 E;RAST:放射过敏原吸附试验;sIgE:特异性 IgE;SIT:特异性免疫疗法;SCIT:皮下免疫疗法;SLIT:舌下免疫疗法;SPT:皮肤点刺试验。