2002
DOI: 10.1016/s0091-6749(02)81282-9
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Th2 cytokine expression in atopic children with otitis media with effusion

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Cited by 10 publications
(21 citation statements)
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“…Jang and Kim [27] found significantly higher levels of allergic mediators such as IL-4, IL-6, and tumor necrosis factor-α in the MEE of the allergic individuals suffering from OM. Sobol et al [28] also found that atopic patients have a significantly higher percentage of T lymphocytes, eosinophils, mast cells, basophils, IL-4, and IL-5 in MEE, and Hurst and Venge [25] reported that mast cells and the mediator tryptase are present in the majority of ears that have chronic effusion. Overall, these results support the hypothesis that the immunopathologic mechanism underlying the development of MEE can be largely a result of the effects of T-helper type 2 (Th2) mediators; thus, the inflammation within the middle ear of many patients is allergic in nature.…”
Section: Role Of Atopymentioning
confidence: 95%
“…Jang and Kim [27] found significantly higher levels of allergic mediators such as IL-4, IL-6, and tumor necrosis factor-α in the MEE of the allergic individuals suffering from OM. Sobol et al [28] also found that atopic patients have a significantly higher percentage of T lymphocytes, eosinophils, mast cells, basophils, IL-4, and IL-5 in MEE, and Hurst and Venge [25] reported that mast cells and the mediator tryptase are present in the majority of ears that have chronic effusion. Overall, these results support the hypothesis that the immunopathologic mechanism underlying the development of MEE can be largely a result of the effects of T-helper type 2 (Th2) mediators; thus, the inflammation within the middle ear of many patients is allergic in nature.…”
Section: Role Of Atopymentioning
confidence: 95%
“…The middle ear effusions of atopic patients with OME showed significantly higher levels of eosinophils, T lymphocytes, and IL-4 mRNA+ cells (p<0.01) and significantly lower levels of neutrophils and IFN-γ mRNA+ cells (p<0.01) compared to non-atopic patients with OME (Nguyen et al, 2004). Similarly, in another study, a higher percentage of eosinophils and T lymphocytes, and a higher percentage of cells expressing IL-4 and IL-5 were found among atopic patients with OME (Sobol et al, 2002). Fireman, 1988) www.intechopen.com…”
Section: Pathophysiology Of Ome and Armentioning
confidence: 76%
“…Furthermore, it has been found that a reduction in the size of the lumen in an inflamed E-tube could impede mucociliary function, thus delaying clearance of acute infective middle ear effusion, leading to recurrent OME (Alles et al, 2001). Several studies analyzing middle ear mucosa and effusions in atopic patients with OME have demonstrated that the composition of the inflammatory substrate in acute otitis media is similar to the type I late-phase allergic response seen in other areas of the respiratory tract, such as in AR, chronic RS, and asthma (Nguyen et al, 2004;Sobol et al, 2002;Hurst, 1996). The middle ear effusions of atopic patients with OME showed significantly higher levels of eosinophils, T lymphocytes, and IL-4 mRNA+ cells (p<0.01) and significantly lower levels of neutrophils and IFN-γ mRNA+ cells (p<0.01) compared to non-atopic patients with OME (Nguyen et al, 2004).…”
Section: Pathophysiology Of Ome and Armentioning
confidence: 99%
“…Alguns autores não observaram interação 22,25 , enquanto outros verificaram associação positiva, sendo os fenômenos atópi-cos considerados fatores de risco para as otites [26][27][28] .…”
Section: Resultsunclassified