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Paediatric obstructive sleep apnoea syndrome (OSAS) is associated with tonsil colonisation by Streptococcus pyogenes

机译:小儿阻塞性睡眠呼吸暂停综合征(OSAS)与化脓性链球菌引起的扁桃体定植有关

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摘要

The involvement of pathogenic bacteria in obstructive sleep apnoea syndrome (OSAS) has yet to be elucidated. We investigated the possible role of group A streptococcus (GAS) in OSAS pathogenesis. In 40 tonsillectomized patients affected by OSAS and 80 healthy controls, significant (p < 0.0001) association of GAS with paediatric OSAS was found. Supernatant from streptolysin O (SLO)-producing GAS induced production of cysteinyl leukotrienes (CysLTs) in tonsil mononuclear cells (TMCs). CysLTs-treated TMCs showed significant (p < 0.05) proliferation of CD4+ T, CD19+ and CD19+CD27+CD38+ B lymphocytes. We discovered a SLO-dependent activation of CysLTs production through a pathway involving TOLL-like receptor 4 (TLR4), TIR-domain-containing adapter-inducing interferon-β (TRIF), Myeloid differentiation primary response gene 88 (MyD88), and p38 MAP Kinase. In conclusion, we hypothesise that GAS may contribute to paediatric tonsillar hyperplasia through CysLTs production induced by SLO, and this might explain its association with OSAS.
机译:致病性细菌参与阻塞性睡眠呼吸暂停综合症(OSAS)的情况尚待阐明。我们调查了在OSAS发病机理中A组链球菌(GAS)的可能作用。在40例受OSAS切除的扁桃体切除患者和80例健康对照者中,发现GAS与儿科OSAS显着相关(p 0.0001)。产生链球菌溶血素O(SLO)的上清液诱导扁桃体单核细胞(TMC)中半胱氨酰白三烯(CysLTs)的产生。 CysLTs处理的TMCs表现出CD4 + T,CD19 +和CD19 + CD27 + CD38 + B淋巴细胞显着(p 0.05)增殖。我们通过涉及TOLL样受体4(TLR4),含TIR域的衔接子诱导干扰素-β(TRIF),髓样分化初级反应基因88(MyD88)和p38的途径发现了CysLTs生产的SLO依赖性激活MAP激酶。总之,我们假设GAS可能通过SLO诱导的CysLTs产生而导致小儿扁桃体增生,这也许可以解释其与OSAS的相关性。

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