首页> 外文期刊>Antimicrobial agents and chemotherapy. >Impact of cethromycin (ABT-773) therapy on microbiological, histologic, immunologic, and respiratory indices in a murine model of Mycoplasma pneumoniae lower respiratory infection.
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Impact of cethromycin (ABT-773) therapy on microbiological, histologic, immunologic, and respiratory indices in a murine model of Mycoplasma pneumoniae lower respiratory infection.

机译:在肺炎支原体下呼吸道感染的小鼠模型中,头孢霉素(ABT-773)治疗对微生物学,组织学,免疫学和呼吸学指标的影响。

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Mycoplasma pneumoniae is a major etiologic agent of acute lower respiratory infections. We evaluated the antimicrobial and immunologic effects of cethromycin (ABT-773), a ketolide antibiotic, for the treatment of M. pneumoniae pneumonia in a mouse model. Eight-week-old BALB/c mice were inoculated intranasally once with 10(6) CFU of M. pneumoniae on day 0. Treatment was started 24 h after inoculation. Groups of mice were treated subcutaneously with cethromycin at 25 mg/kg of body weight or with placebo daily until sacrifice. Five to ten mice per group were evaluated at days 1, 4, 7, and 10 after inoculation. Outcome variables included bronchoalveolar lavage (BAL) for M. pneumoniae quantitative culture and cytokine and chemokine concentration determinations by enzyme-linked immunosorbent assay (tumor necrosis factor alpha [TNF-alpha], gamma interferon [IFN-gamma], interleukin-1beta [IL-1beta], IL-2, IL-4, IL-12, granulocyte-macrophage colony-stimulating factor, IL-8, monocyte chemoattractant protein 1 [MCP-1], and macrophage inflammatory protein 1alpha [MIP-1alpha]), histopathologic score of the lungs (HPS), and pulmonary function tests (PFT) using whole-body, unrestrained plethysmography at the baseline and post-methacholine exposure as indicators of airway obstruction (AO) and airway hyperresponsiveness (AHR), respectively. The cethromycin-treated mice had a greater reduction in M. pneumoniae culture titers than placebo-treated mice, reaching statistical significance on days 7 and 10 (P < 0.05). HPS was significantly reduced in cethromycin-treated mice compared with placebo-treated mice on days 4, 7, and 10 (P < 0.05). Cytokine concentrations in BAL samples were reduced in mice that received cethromycin, and the differences were statistically significant for 7 of the 10 cytokines measured (TNF-alpha, IFN-gamma, IL-1beta, IL-8, IL-12, MCP-1, and MIP-1alpha) on day 4 (P < 0.05). PFT values were improved in the cethromycin-treated mice, with AO and AHR significantly reduced on day 4 (P < 0.05). In this mouse model, treatment with cethromycin significantly reduced M. pneumoniae culture titers in BAL samples, cytokine and chemokine concentrations in BAL samples, histologic inflammation in the lungs, and disease severity as defined by AO and AHR.
机译:肺炎支原体是急性下呼吸道感染的主要病因。我们评估了头霉素的头孢霉素(ABT-773)的抗微生物和免疫学作用,其在小鼠模型中用于治疗肺炎支原体肺炎。在第0天,将8周龄的BALB / c小鼠鼻内接种10(6)CFU的肺炎支原体。在接种后24小时开始治疗。每天用25 mg / kg体重的红霉素皮下或每天用安慰剂皮下治疗小鼠,直至处死。接种后第1、4、7和10天,每组评估五到十只小鼠。结果变量包括用于肺炎支原体定量培养的支气管肺泡灌洗(BAL)以及通过酶联免疫吸附测定(肿瘤坏死因子α[TNF-α],γ干扰素[IFN-γ],白介素-1β[IL]测定细胞因子和趋化因子浓度)。 -1β,IL-2,IL-4,IL-12,粒细胞-巨噬细胞集落刺激因子,IL-8,单核细胞趋化蛋白1 [MCP-1]和巨噬细胞炎症蛋白1alpha [MIP-1alpha]),分别采用全身,基线无约束性容积描记法和美索胆碱暴露后的全身肺组织病理学评分(HPS)和肺功能测试(PFT)作为气道阻塞(AO)和气道高反应性(AHR)的指标。与安慰剂处理的小鼠相比,用红霉素处理的小鼠的肺炎支原体培养滴度降低幅度更大,在第7天和第10天达到统计学显着性(P <0.05)。与安慰剂处理的小鼠相比,在第4、7和10天,用红霉素处理的小鼠的HPS显着降低(P <0.05)。接受红霉素的小鼠的BAL样品中的细胞因子浓度降低,并且所测量的10种细胞因子中的7种(TNF-alpha,IFN-γ,IL-1beta,IL-8,IL-12,MCP-1)的差异具有统计学意义和第4天的MIP-1alpha)(P <0.05)。在用红霉素处理的小鼠中,PFT值有所改善,在第4天AO和AHR显着降低(P <0.05)。在此小鼠模型中,用红霉素处理可显着降低BAL样品中的肺炎支原体培养效价,BAL样品中的细胞因子和趋化因子浓度,肺部组织学炎症以及AO和AHR定义的疾病严重程度。

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