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Evaluation of Th17-related cytokines and IFNγ production from blood mononuclear cells of moderate and severe asthmatic children reveals methylprednisolone does not decrease IL-22 levels
Authors:Emanuel Sávio Cavalcanti Sarinho  Adriana Azoubel-Antunes  Moacyr Jesus Barreto de Melo Rêgo  Mariana Brayner-Cavalcanti  Thiago Ubiratan Lins e Lins  Ivan Da Rocha Pitta
Institution:1. Servi?o de Alergia e Imunologia Clínica, Hospital das Clínicas, Universidade Federal de Pernambuco (UFPE), Recife, Brasil and;2. Laboratório de Imunomodula??o e Novas Abordagens Terapêuticas (LINAT), Núcleo de pesquisas em inova??o terapêutica (NUPIT), Universidade Federal de Pernambuco (UFPE), Recife, Brasil
Abstract:Objective: The aim of this study was to correlate IL-6, IL-17A, IFNγ, and IL-22 production with asthma disease severity and to evaluate if methylprednisolone downregulated cytokine production in peripheral blood mononuclear cells (PBMCs). Methods: Forty-two children with chronic persistent asthma and 34 non-asthmatic children were selected. Cytokines were quantified by ELISA from serum or PBMCs supernatants, after the PMA and Ionomycin stimulation, with or without methylprednisolone at 100?µM. Results: Our data showed undetectable levels of serum cytokines in most patients and controls. In the PBMCs, we have observed a higher production of IL-17A than IL-22 among asthmatics and controls, although it is not statistically significant. IL-6, IFNγ, and IL-17A levels were significantly reduced after methylprednisolone treatment (p?=?0.02, 0.03, and 0.03, respectively) in Severe Persistent Asthma (SPA) and in Moderate Persistent Asthma (MPA), (p?=?0.007, 0.01, and 0.007, respectively). However, IL-22 levels were unaffected (SPA, p?=?0.12 and MPA, p?=?0.93). Conclusion: Methylprednisolone downregulated IL-6, IL17A, and IFNγ, but not IL-22, in stimulated PBMCs from asthmatic children indicating that methylprednisolone has no effect on IL-22 production by PBMCs.
Keywords:Immunomodulation  interferon gamma  interleukin  interleukin 17  interleukin 22  treatment
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