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金黄色葡萄球菌肠毒素 B 有助于诱导变应性鼻炎鼻窦炎模型中的鼻息肉样病变。

Staphylococcus aureus enterotoxin B contributes to induction of nasal polypoid lesions in an allergic rhinosinusitis murine model.

机构信息

Department of Otorhinolaryngology, Gyeongsang National University, Jinju, Korea.

出版信息

Am J Rhinol Allergy. 2011 Nov-Dec;25(6):e255-61. doi: 10.2500/ajra.2011.25.3727.


DOI:10.2500/ajra.2011.25.3727
PMID:22185735
Abstract

BACKGROUND: Studies on the pathophysiology of nasal polyps in human subjects have been limited; thus an animal model is needed. There is increasing evidence supporting the role of Staphylococcus aureus enterotoxin B (SEB) in the pathogenesis of nasal polyposis. The aim of this study was to investigate the histological and immunologic effects of SEB on the formation of nasal polypoid lesions in an allergic rhinosinusitis murine model. METHODS: After induction of an ovalbumin (OVA)-induced allergic rhinosinusitis, OVA with SEB (5 or 500 ng) was instilled into the nasal cavity of mice for 8 weeks. Control mice did not receive SEB or OVA instillation. Histopathological changes were observed using hematoxylin and eosin, Sirius red, Giemsa, Masson's trichrome, and Alcian blue stains. The levels of interleukin (IL)-4, IL-5, IL-8, IL-13, eotaxin, interferon gamma, total IgE, and OVA-specific IgE from serum or nasal lavage fluid were measured using enzyme-linked immunosorbent assay. RESULTS: The group treated with OVA plus 5 ng of SEB had significantly more mucosal lesions with epithelial disruption and nasal polypoid lesions than mice treated with OVA only, showing a significant increase in the infiltration of total inflammatory cells, eosinophils, and lymphocytes than the other groups. Levels of IL-5, eotaxin, and OVA-specific IgE in nasal lavage fluid were increased in the group treated with OVA plus 5 ng of SEB than in the other groups. A higher number of secretory cells in the groups treated with OVA plus SEB was observed than in other groups. CONCLUSION: Low-dose SEB induced nasal polypoid lesions with an increased eosinophilic infiltration in an allergic rhinosinusitis murine model.

摘要

背景:对人体鼻息肉病理生理学的研究受到限制;因此需要建立动物模型。越来越多的证据支持金黄色葡萄球菌肠毒素 B(SEB)在鼻息肉病发病机制中的作用。本研究旨在探讨 SEB 对变应性鼻炎鼻窦炎小鼠模型鼻息肉样病变形成的组织学和免疫学影响。

方法:在卵清蛋白(OVA)诱导的变应性鼻炎鼻窦炎后,将 OVA 与 SEB(5 或 500 ng)注入小鼠鼻腔 8 周。对照组小鼠未接受 SEB 或 OVA 滴注。使用苏木精和伊红、天狼猩红、吉姆萨、马松三色和阿利新蓝染色观察组织病理学变化。使用酶联免疫吸附试验测量血清或鼻洗液中白细胞介素(IL)-4、IL-5、IL-8、IL-13、嗜酸性粒细胞趋化因子、干扰素γ、总 IgE 和 OVA 特异性 IgE 的水平。

结果:用 OVA 加 5ng SEB 处理的组比仅用 OVA 处理的组具有更多的粘膜病变和上皮破坏以及鼻息肉样病变,与其他组相比,总炎性细胞、嗜酸性粒细胞和淋巴细胞的浸润显著增加。用 OVA 加 5ng SEB 处理的组的鼻洗液中 IL-5、嗜酸性粒细胞趋化因子和 OVA 特异性 IgE 的水平均高于其他组。与其他组相比,用 OVA 加 SEB 处理的组中分泌细胞的数量增加。

结论:低剂量 SEB 在变应性鼻炎鼻窦炎小鼠模型中诱导鼻息肉样病变,并增加嗜酸性粒细胞浸润。

相似文献

[1]
Staphylococcus aureus enterotoxin B contributes to induction of nasal polypoid lesions in an allergic rhinosinusitis murine model.

Am J Rhinol Allergy. 2011

[2]
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Allergol Immunopathol (Madr). 2016

[3]
Interleukin-17A-induced inflammation does not influence the development of nasal polyps in murine model.

Int Forum Allergy Rhinol. 2015-5

[4]
Repeated intranasal instillation with staphylococcal enterotoxin B induces nasal allergic inflammation in guinea pigs.

Am J Rhinol Allergy. 2011

[5]
Histological and immunological observations of bacterial and allergic chronic rhinosinusitis in the mouse.

Am J Rhinol. 2008

[6]
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Rhinology. 2024-8-1

[7]
Aggravation of bronchial eosinophilia in mice by nasal and bronchial exposure to Staphylococcus aureus enterotoxin B.

Clin Exp Allergy. 2006-8

[8]
Blocking interleukin-17 attenuates enhanced inflammation by staphylococcal enterotoxin B in murine allergic rhinitis model.

Acta Otolaryngol. 2012-6

[9]
Proinflammatory impact of Staphylococcus aureus enterotoxin B on human nasal epithelial cells and inhibition by dexamethasone.

Am J Rhinol Allergy. 2009

[10]
Nasal exposure to Staphylococcal enterotoxin enhances the development of allergic rhinitis in mice.

Clin Exp Allergy. 2005-4

引用本文的文献

[1]
The advance on pathophysiological mechanisms of type 2 chronic rhinosinusitis with nasal polyposis.

Front Allergy. 2025-7-2

[2]
Induced Chronic Rhinosinusitis in Rats Leads to Secondary Changes in Sinonasal Microbiota.

Laryngoscope Investig Otolaryngol. 2025-7-7

[3]
Inotodiol Attenuates Mucosal Inflammation in a Mouse Model of Eosinophilic Chronic Rhinosinusitis.

Allergy Asthma Immunol Res. 2025-1

[4]
Gαi1/3 signaling mediates IL-5-induced eosinophil activation and type 2 inflammation in eosinophilic chronic rhinosinusitis.

Front Immunol. 2025-1-7

[5]
The role and mechanism of HMGB1-mediated Notch1/Hes-1 pathway in anxiety and depression-like behaviors in mice with chronic rhinosinusitis.

Mol Med. 2025-1-9

[6]
Novel insights into the immune response to bacterial T cell superantigens.

Nat Rev Immunol. 2024-6

[7]
Induction of a type 2 inflammatory chronic rhinosinusitis in C57BL/6 mice.

Asia Pac Allergy. 2023-12

[8]
Host-microbe interactions in chronic rhinosinusitis biofilms and models for investigation.

Biofilm. 2023-9-29

[9]
Murine model for chronic rhinosinusitis: an interventional study.

J Otolaryngol Head Neck Surg. 2023-4-25

[10]
TIM-4 in macrophages contributes to nasal polyp formation through the TGF-β1-mediated epithelial to mesenchymal transition in nasal epithelial cells.

Front Immunol. 2022

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