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Chronic widespread dermatophytosis due to Trichophyton rubrum: a syndrome associated with a Trichophyton-specific functional defect of phagocytes

机译:毛癣菌引起的慢性广泛性皮肤癣菌症:一种与吞噬细胞特有的癣菌特定功能缺陷有关的综合征

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摘要

Dermatophytes are agents of typically benign superficial infections. However, an increasing number of severe infections in immunocompromised hosts has been reported. We aimed to understand the factors underlying the existence of a cohort of patients presenting with chronic widespread dermatophytosis (CWD) due to Trichophyton rubrum, but with no signs of immunodeficiency. Their disease is usually recurrent and difficult to manage. Fourteen patients meeting the following criteria for CWD were studied: T. rubrum culture-proven skin lesions of ≥10 cm in at least one dimension; the involvement of at least three non-contiguous localizations of >1 year’s duration; and no predisposing conditions. For comparison, we also studied 13 acute Tinea pedis patients. Macrophages and neutrophils were isolated and tested for T. rubrum conidia phagocytic and killing activity. H2O2, NO, and pro- and anti-inflammatory cytokine release were measured. All experiments were run with age- and sex-matched healthy donors’ cells in parallel. CWD patients’ macrophages and neutrophils presented with reduced T. rubrum–phagocytic and killing abilities, and reduced H2O2 and NO release when compared with those of healthy donors. CWD patients’ macrophages secreted lower levels of the proinflammatory cytokines interleukin (IL)-1β, IL-6, IL-8, and tumor necrosis factor (TNF)-α, but enhanced levels of the anti-inflammatory cytokine IL-10. Neutrophil secretion closely followed this unbalanced pattern. In contrast, responses to the positive controls zymosan, lipopolysaccharide, and phorbol myristate acetate were comparable with those of healthy donors. The same experiments were performed with macrophages and neutrophils from the acute Tinea pedis patients and showed no differences when compared with the matched healthy donors. Patients with CWD have a T. rubrum-related functional deficiency of phagocytes and may represent a distinct clinical entity in the complex spectrum of the Trichophyton–host interaction.
机译:皮肤癣菌是典型的良性浅表感染的媒介。然而,已经报道了在免疫受损的宿主中越来越多的严重感染。我们旨在了解导致因毛癣菌而出现慢性广泛性皮肤癣菌症(CWD)的患者队列的潜在因素,但没有免疫缺陷的迹象。他们的疾病通常是复发的并且难以治疗。研究了14个满足以下CWD标准的患者:红毛锥菌培养证明的至少一维≥10 cm皮肤损伤;至少三个持续时间超过1年的不连续本地化的参与;而且没有任何诱因。为了进行比较,我们还研究了13例急性足癣患者。分离巨噬细胞和嗜中性粒细胞并测试其红锥虫分生孢子的吞噬和杀伤活性。测量了H2O2,NO以及促炎和抗炎细胞因子的释放。所有实验都是在年龄和性别相匹配的健康供体细胞平行进行的。与健康供体相比,CWD患者的巨噬细胞和中性粒细胞具有降低的红斑球菌吞噬和杀伤能力,以及减少的H2O2和NO释放。 CWD患者的巨噬细胞分泌的促炎细胞因子白介素(IL)-1β,IL-6,IL-8和肿瘤坏死因子(TNF)-α的水平较低,但抗炎细胞因子IL-10的水平升高。中性粒细胞的分泌紧密地遵循这种不平衡的模式。相反,对阳性对照酵母聚糖,脂多糖和肉豆蔻酸乙酸酯的反应与健康供体的反应相当。对来自急性足癣患者的巨噬细胞和嗜中性粒细胞进行了相同的实验,与相匹配的健康供体相比没有差异。患有CWD的患者患有红毛球菌相关的吞噬细胞功能缺陷,并且可能在毛癣菌-宿主相互作用的复杂光谱中代表了独特的临床实体。

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