Abstract:Objective: Eosinophilic otitis media (EOM) is an intractable middle ear disease recognized by an eosinophil enriched middle ear effusion and mucosa. Although precise pathogenesis of EOM remains unclear, it is characterized by type 2 inflammation. Since IgG4 is an IgG subclass induced by type 2 cytokines such as IL-4 and IL-13, we sought to characterize and compare local IgG4 expression in patients with and without EOM. Methods: Twelve patients with bilateral profound hearing loss, 9 of which underwent a cochle… Show more
“…En cuanto a la relación entre otitis media eosinofílica y ER-IgG4, en un estudio se sugiere que la ER-IgG4 puede contribuir al desarrollo de esta, aunque solo en 2 de los 48 pacientes de nuestra revisión se les diagnosticó una OME 47 . Con lo cual parece más una presentación excepcional dentro de la ER-IgG4.…”
“…En cuanto a la relación entre otitis media eosinofílica y ER-IgG4, en un estudio se sugiere que la ER-IgG4 puede contribuir al desarrollo de esta, aunque solo en 2 de los 48 pacientes de nuestra revisión se les diagnosticó una OME 47 . Con lo cual parece más una presentación excepcional dentro de la ER-IgG4.…”
“…Previous studies have not provided analyses of the OME effusion proteome database or disease differential analyses. [4][5][6] With advancements in proteomic techniques, a more inclusive analysis is needed to realize the function of middle ear effusion. Moreover, previous studies have indicated that the pathogenesis of OME is associated with immune response, coagulation activities, and inflammatory disorders.…”
Section: Introductionmentioning
confidence: 99%
“…OME was defined as an infection-free disease in the past. 4 However, recent studies have challenged this definition by demonstrating bacterial colonization in the middle ear charge or mucosa of patients with OME. These findings have raised questions regarding the existing theories of the disease’s etiology.…”
Background: Proteins found in middle ear effusion play crucial roles in the physiological and pathological processes of otitis media with effusion (OME), influencing the etiology and clinical characteristics of this disease. The qualitative and quantitative composition of these proteins depending on the underlying pathogenesis of middle ear effusion. Understanding their physiological and pathological functions is of great importance. Methods: We collected samples from 19 volunteers diagnosed with OME. After offline separation using high-pH reversed-phase liquid chromatography (RPLC), the pooled sample was subjected to LC-MS/MS analysis to obtain a comprehensive profile of the OME proteome. Functional analysis was performed using Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Ingenuity Pathway Analysis (IPA) annotations. Data-independent acquisition (DIA) technology was utilized to analyze samples and fix whether the OME proteome could replicate the pathophysiological features associated with this disease. We conducted a differential proteomic analysis between patients with simple OME and patients who had received radiotherapy. The radiotherapyreduced group was further divided into two subgroups: nasopharyngeal carcinoma (NPC) and other types of carcinoma. Parallel reaction monitoring (PRM) technology was used for validation of 36 differentially expressed proteins (DEPs). Results: A number of 732 proteins were identified in the OME proteome database. Among them, 527 proteins were quantified using peak intensity-based semi-quantification (iBAQ), covering a wide dynamic range of approximately 8 orders of magnitude. Based on the functional analysis, we proposed a hypothetical mechanism of OME.
Conclusion:This study managed to put up an inclusive analysis of the OME proteome, establishing the first human OME proteome database. We focused on differential proteomic analysis among different groups to gain a more comprehensive concept of the OME proteome and search for meaningful biomarkers.
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