The role of Staphylococcus aureus enterotoxin B in chronic rhinosinusitis with nasal polyposis

• Published in: Cell communication and signaling Vol. 20; no. 1; p. 29
• Main Authors: Chegini, Zahra, Didehdar, Mojtaba, Khoshbayan, Amin, Karami, Jafar, Yousefimashouf, Milad, Shariati, Aref
• Format: Journal Article
• Language: English
• Published: England BioMed Central 09-03-2022; BMC
• Subjects: Animals; Chronic Disease; Chronic rhinosinusitis; Enterotoxin B; Enterotoxins - pharmacology; Humans; Inflammation - complications; Nasal polyps; Nasal Polyps - complications; Nasal Polyps - metabolism; Review; Rhinitis - complications; Rhinitis - microbiology; Sinusitis - complications; Sinusitis - microbiology; Staphylococcus aureus; Type 2/Th2 pathway; Enterotoxin B; Type 2/Th2 pathway; Chronic rhinosinusitis; Nasal polyps; Staphylococcus aureus
• ISSN: 1478-811X; 1478-811X
• DOI: 10.1186/s12964-022-00839-x

CRS with nasal polyps (CRSwNP) is a multifactorial disease, and various etiological factors like bacterial superantigens are known to develop this disease. Recent studies reported that Staphylococcus aureus nasal colonization was detected in 67% of the patients with CRSwNP. Moreover, it was reported that specific IgE against S. aureus enterotoxins are discovered in almost half of the nasal tissue homogenates from nasal polyps. Thus, investigations have highlighted the role of staphylococcal enterotoxins, especially enterotoxin B (SEB), in pathogenesis of CRSwNP. The destruction of mucosal integrity was reported as a main SEB-related pathogenic mechanisms in CRSwNP. SEB activates Toll Like Receptor 2 and triggers the production of pro-inflammatory cytokines; furthermore, it induces reactive oxygen species and endoplasmic reticulum stress-induced inflammation that may cause epithelial cell integrity disruption and enhance their permeability. SEB-induced Type 2/Th2 pathway results in degranulation of eosinophils, cationic proteins production, and localized eosinophilic inflammation. Furthermore, SEB may be involved in the expression of RORC and HIF-1α in Tregs and by maintaining the inflammation in sinonasal mucosa that could have a main role in the pathogenesis of nasal polyposis. Different in vitro findings were confirmed in animal studies; however, in vivo analysis of SEB-induced nasal polyps and CRS remains unfulfilled due to the lack of appropriate animal models. Finally, after elucidating different aspects of SEB pathogenesis in CRSwNP, therapeutic agents have been tested in recent studies with some encouraging results. The purpose of this article is to summarize the most important findings regarding SEB-induced CRS and nasal polyposis. Video Abstract.