Literature DB >> 15654214

Superantigen hypothesis for the early development of chronic hyperplastic sinusitis with massive nasal polyposis.

Joel M Bernstein1, Rita Kansal.   

Abstract

PURPOSE OF REVIEW: The pathogenesis, pathophysiology, and immunobiology of chronic hyperplastic sinusitis with massive nasal polyposis are starting to become unraveled. Allergy, viral infection, bacterial infection, fungal infection, and environmental pollution have all been suggested as possible initial triggers that may upregulate inflammation of the lateral wall of the nose to develop nasal polyposis. The purpose of this review is to present data from our laboratory that suggest that one of the possible early events in the development of inflammation of the lateral wall of the nose in chronic hyperplastic sinusitis with massive nasal polyposis is the production of exotoxins from Staphylococcus aureus. The exotoxins may act as superantigens and cause activation and clonal expansion of lymphocytes with specific Vbeta regions, resulting in massive cytokine production. RECENT
FINDINGS: Recent published studies suggest that S. aureus is the most common organism isolated from the mucus adjacent to massive nasal polyposis. Staphylococci produce exotoxins. These exotoxins, sometimes known as enterotoxins, include SEA, SEB, and TSST-1. These exotoxins are capable of acting as superantigens and therefore, reacting with T lymphocytes with specific Vbetas in the lateral wall of the nose. Thereafter, it is possible that these lymphocytes are stimulated to produce both TH1 and TH2 cytokines, which have also been demonstrated in the nasal polyp. The consequence of these findings may be the upregulation and increased survival of eosinophils in the nasal polyp.
SUMMARY: Staphylococcus aureus is present in the mucin adjacent to nasal polyps in about 60 to 70% of cases of massive nasal polyposis. These organism, as studied up to the present, always produce exotoxins, which may act as superantigens, causing activation and clonal expansion of lymphocytes with specific Vbeta region in the lateral wall of the nose. The present review suggests that activation of these lymphocytes produce both TH1 and TH2 cytokines. The potential damage to the nasal mucosa from eosinophils is briefly discussed. Theoretically, topical antibiotics to suppress the colonization of S. aureus may be a logical approach to downregulate the production of superantigen in the lateral wall of the nose after appropriate endoscopic sinus surgery.

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Year:  2005        PMID: 15654214     DOI: 10.1097/00020840-200502000-00010

Source DB:  PubMed          Journal:  Curr Opin Otolaryngol Head Neck Surg        ISSN: 1068-9508            Impact factor:   2.064


  14 in total

1.  Induction of CXC chemokines in A549 airway epithelial cells by trypsin and staphylococcal proteases - a possible route for neutrophilic inflammation in chronic rhinosinusitis.

Authors:  F Sachse; C von Eiff; W Stoll; K Becker; C Rudack
Journal:  Clin Exp Immunol       Date:  2006-06       Impact factor: 4.330

2.  Altered expression of genes associated with innate immunity and inflammation in recalcitrant rhinosinusitis with polyps.

Authors:  Andrew P Lane; Quynh Ai Truong-Tran; Robert P Schleimer
Journal:  Am J Rhinol       Date:  2006 Mar-Apr

3.  Different roles of Staphylococcus aureus enterotoxin in different subtypes of nasal polyps.

Authors:  Ke-Jia Cheng; Shen-Qing Wang; Ying-Ying Xu
Journal:  Exp Ther Med       Date:  2016-12-02       Impact factor: 2.447

4.  Screening for staphylococcal superantigen genes shows no correlation with the presence or the severity of chronic rhinosinusitis and nasal polyposis.

Authors:  Frédéric Heymans; Adrien Fischer; Nicholas W Stow; Myriam Girard; Zacharias Vourexakis; Antoine Des Courtis; Gesuele Renzi; Elzbieta Huggler; Stefan Vlaminck; Pierre Bonfils; Ranko Mladina; Valerie Lund; Jacques Schrenzel; Patrice François; Jean Silvain Lacroix
Journal:  PLoS One       Date:  2010-03-05       Impact factor: 3.240

5.  Are neutrophil, platelet and eosinophil-to-lymphocyte ratio and red blood cell distribution width can be used for nasal polyposis?

Authors:  Ahmet Kara; Mehmet Guven; Mahmut Sinan Yilmaz; Deniz Demir; Halil Elden
Journal:  Eur Arch Otorhinolaryngol       Date:  2017-11-30       Impact factor: 2.503

6.  Understanding the Role of Biofilms and Superantigens in Chronic Rhinosinusitis.

Authors:  Ivy W Maina; Neil N Patel; Noam A Cohen
Journal:  Curr Otorhinolaryngol Rep       Date:  2018-07-26

Review 7.  Differential diagnosis of eosinophilic chronic rhinosinusitis.

Authors:  John C Sok; Berrylin J Ferguson
Journal:  Curr Allergy Asthma Rep       Date:  2006-05       Impact factor: 4.919

8.  Rhinosinusitis derived Staphylococcal enterotoxin B possibly associates with pathogenesis of ulcerative colitis.

Authors:  Ping-Chang Yang; Tao Liu; Bin-Quan Wang; Tao-Yuan Zhang; Zi-Yuan An; Peng-Yuan Zheng; Dao-Fa Tian
Journal:  BMC Gastroenterol       Date:  2005-09-06       Impact factor: 3.067

9.  Lipopolysaccharide induces pro-inflammatory cytokines and MMP production via TLR4 in nasal polyp-derived fibroblast and organ culture.

Authors:  Jung-Sun Cho; Ju-Hyung Kang; Ji-Young Um; In-Hye Han; Il-Ho Park; Heung-Man Lee
Journal:  PLoS One       Date:  2014-11-12       Impact factor: 3.240

10.  Mometasone implant for chronic rhinosinusitis.

Authors:  Calvin C Wei; David W Kennedy
Journal:  Med Devices (Auckl)       Date:  2012-08-17
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