Differential expression of periostin in the nasal polyp may represent distinct histological features of chronic rhinosinusitis

2015 ◽  
Vol 42 (2) ◽  
pp. 123-127 ◽  
Author(s):  
Osamu Shiono ◽  
Yasunori Sakuma ◽  
Masanori Komatsu ◽  
Mariko Hirama ◽  
Yukiko Yamashita ◽  
...  
Author(s):  
Yeong-Kyu Park ◽  
Sung Tae Seo ◽  
Eung Hyup Kim ◽  
Dong-Hyun Kim ◽  
Jin Woong Choi ◽  
...  

2012 ◽  
Vol 39 (1) ◽  
pp. 38-47 ◽  
Author(s):  
Yuichi Majima ◽  
Yuichi Kurono ◽  
Katsuhiro Hirakawa ◽  
Keiichi Ichimura ◽  
Shinichi Haruna ◽  
...  

2017 ◽  
Vol 31 (6) ◽  
pp. 352-356 ◽  
Author(s):  
Sarah E. Smith ◽  
Rodney J. Schlosser ◽  
James R. Yawn ◽  
Jose L. Mattos ◽  
Zachary M. Soler ◽  
...  

Background CD8+ T cells and natural killer (NK) cells are cytotoxic cells that use granzyme B (GrB) and perforin. Defective cytotoxic function is known to play a role in dysregulated immune response as seen in chronic sinusitis, also referred to as chronic rhinosinusitis (CRS). However, to our knowledge, in the United States, neither GrB or perforin expression has been reported in patients with CRS. Objective The aim of this study was to investigate sinonasal cytotoxic cells, their mediators, and cell-specific distribution of these mediators in patients with CRS with nasal polyp (CRSwNP) and in patients with CRS without nasal polyp (CRSsNP). Methods Blood and sinus tissue samples were taken from patients with CRSsNP (n = 8) and CRSwNP (n = 8) at the time of surgery. Control subjects (n = 8) underwent surgery for cerebrospinal fluid leak repair or to remove non-hormone-secreting pituitary tumors. The cells were analyzed via flow cytometry by using CD8 expression to identify cytotoxic T cells and CD56 expression to identify NK cells. Intracellular GrB and perforin expression were analyzed with flow cytometry. Results We observed no significant differences in plasma or peripheral blood immune cell numbers or specific levels of GrB or perforin among the groups. In the sinonasal mucosa of the patients with CRSsNP and the patients with CRSwNP, there was a significant decrease in GrB and perforin levels (p <0.05) despite similar or increased numbers of cytotoxic cells when compared with the controls. The overall decrease in GrB and perforin in the sinonasal mucosa of the patients with CRSsNP and the patients with CRSwNP was due to decreased T cell production. There was no difference in total NK cell count or expression of perforin or GrB among all the groups. Conclusion Total levels of sinonasal GrB and perforin were decreased in the sinonasal mucosa of both the patients with CRSwNP and the patients with CRSsNP compared with the controls, whereas sinonasal CD8+ T cells, (but not NK cells,), intracellular stores of GrB and perforin were reduced in the patients with CRSwNP compared with the controls.


Allergy ◽  
2012 ◽  
Vol 67 (7) ◽  
pp. 920-928 ◽  
Author(s):  
S. Seshadri ◽  
D. C. Lin ◽  
M. Rosati ◽  
R. G. Carter ◽  
J. E. Norton ◽  
...  

2013 ◽  
Vol 131 (2) ◽  
pp. AB225
Author(s):  
Sudarshan Seshadri ◽  
Xiang Lu ◽  
Andrew Choi ◽  
Roderick Carter ◽  
James Norton ◽  
...  

Author(s):  
Soo Kyoung Park ◽  
Rui-Ning Han ◽  
Jun Xu ◽  
Sun Hee Yeon ◽  
Sung Bok Lee ◽  
...  

Background and Objectives The nucleotide-binding oligomerization domain-like receptor (NLRP) 3 is known as a member of the NLR family, and it has been confirmed that the NLRP3 inflammasome is associated with various diseases such as asthma, inflammatory bowel disease, metabolic disorders and multiple sclerosis, as well as other auto-immune and auto-inflammatory diseases. However, the role of NLRP3 in chronic rhinosinusitis with nasal polyps (CRSwNP) has not yet been explored.Subjects and Method Forty-four specimens of nasal polyps and 25 specimens of uncinate processes were collected from patients with chronic rhinosinusitis with nasal polyps, and 25 specimens of uncinate tissues were collected from patients who underwent other rhino-surgeries. The western blot assay was employed to analyze the expression of NLRP3; interleukin (IL)-1β and IL-17A were detected using immunohistochemistry and real-time polymerase chain reaction. The production of lipopolysaccharide (LPS) induced IL-1β and IL-17A with or without the NLRP3 inflammasome inhibitor (MCC950) was measured using an enzyme linked immunosorbent assay in cultured dispersed nasal polyp cells.Results NLRP3 showed a high level of expression in nasal polyps than in the control group (<i>p</i><0.01). The expression of IL-1β and IL-17A was significantly higher in nasal polyps in the CRSwNP group than in the control group (<i>p</i><0.05). LPS-induced production of IL-1β was significantly suppressed by treatment with the NLRP3 inflammasome inhibitor (<i>p</i><0.05).Conclusion The NLRP3 inflammasome plays an essential role in the pathogenesis of CRSwNP, and thus MCC950 can be considered a prospective therapeutic for NLRP3 inflammasome-mediated inflammation in nasal polyps. Our data provide new evidence that IL-17A is involved in inflammasome-associated inflammation in nasal polyps.


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