Department of Pharmacology and Experimental Therapeutics, School of Pharmacy Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Otolaryngology/Head and Neck Surgery, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
Int Arch Allergy Immunol. 2021;182(10):962-970. doi: 10.1159/000515918. Epub 2021 Apr 28.
The pathogenesis of chronic rhinosinusitis (CRS) with nasal polyps (CRSwNPs) is not yet completely understood. Based on current knowledge, the infiltration of mast cells and eosinophils in nasal polyps (NPs) plays an important role. This study aimed to investigate the interplay of asthma and allergy etiopathology in CRSwNPs patients by specifically studying tissue mast cells and eosinophils and the pro-inflammatory marker CD48.
Immunohistochemistry was used to assess eosinophils, mast cells, and CD48 expressing eosinophils infiltrating NPs, and flow cytometry was used to assess surface receptors expression on eosinophils from digested NPs.
Immunohistochemical analyses showed that mast cell infiltration in NPs is higher in allergic patients in comparison to nonallergic patients; eosinophils infiltration in asthmatic NPs was significantly elevated in comparison to the nonasthmatic NPs, and membrane CD48 (mCD48) expression on eosinophils infiltrating nonallergic asthmatic NPs was highly elevated in comparison to the other subgroups. Similarly, mCD48 and its high-affinity ligand m2B4's expression on eosinophils from enzymatically digested NPs were significantly higher in nonallergic asthmatics in comparison to allergic asthmatics.
Eosinophil infiltration in NPs for asthmatic patients, and mast cell infiltration for allergic patients, may be used as reliable biomarkers for endotyping CRSwNPs. In addition, CD48 in asthmatic patients who developed CRSwNPs could be regarded as a potential target for treatment.
慢性鼻-鼻窦炎伴鼻息肉(CRSwNPs)的发病机制尚未完全阐明。基于现有知识,鼻息肉(NPs)中肥大细胞和嗜酸性粒细胞的浸润起着重要作用。本研究旨在通过专门研究组织肥大细胞和嗜酸性粒细胞以及促炎标志物 CD48,来探讨哮喘和过敏病因在 CRSwNPs 患者中的相互作用。
采用免疫组织化学法评估嗜酸性粒细胞、肥大细胞和表达 CD48 的嗜酸性粒细胞浸润 NP,采用流式细胞术评估从消化的 NP 中分离的嗜酸性粒细胞表面受体的表达。
免疫组织化学分析表明,与非过敏患者相比,NP 中肥大细胞浸润在过敏患者中更高;与非哮喘 NP 相比,哮喘 NP 中的嗜酸性粒细胞浸润显著升高,与其他亚组相比,非过敏哮喘 NP 中浸润的嗜酸性粒细胞的膜 CD48(mCD48)表达显著升高。同样,与过敏哮喘患者相比,非过敏哮喘患者从酶消化 NP 中分离的嗜酸性粒细胞上 mCD48 及其高亲和力配体 m2B4 的表达显著升高。
对于哮喘患者,NP 中的嗜酸性粒细胞浸润,对于过敏患者,肥大细胞浸润,可能作为 CRSwNPs 分型的可靠生物标志物。此外,在发生 CRSwNPs 的哮喘患者中,CD48 可被视为潜在的治疗靶点。