Salvatore C M, Fonseca-Aten M, Katz-Gaynor K, Gomez A M, Mejias A, Somers C, Chavez-Bueno S, McCracken G H, Hardy R D
Department of Pediatric Infectious Diseases, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9063, USA.
Infect Immun. 2007 Jan;75(1):236-42. doi: 10.1128/IAI.01249-06. Epub 2006 Oct 30.
Mycoplasma pneumoniae is a leading cause of pneumonia and is associated with asthma. Evidence links M. pneumoniae respiratory disease severity with interleukin-12 (IL-12) concentration in respiratory secretions. We evaluated the microbiologic, inflammatory, and pulmonary function indices of M. pneumoniae pneumonia in IL-12 (p35) knockout (KO) mice and wild-type (WT) mice to determine the role of IL-12 in M. pneumoniae respiratory disease. Eight-week-old wild-type BALB/c mice and 8-week-old IL-12 (p35) KO BALB/c mice were inoculated once intranasally with 10(7) CFU of M. pneumoniae. Mice were evaluated at days 2, 4, and 7 after inoculation. Outcome variables included quantitative bronchoalveolar lavage (BAL) M. pneumoniae culture, lung histopathologic scores (HPS), BAL cytokine concentrations determined by enzyme-linked immunosorbent assay (tumor necrosis factor alpha [TNF-alpha], gamma interferon [IFN-gamma], IL-1beta, IL-2, IL-4, IL-5, IL-6, IL-10, and granulocyte-macrophage colony-stimulating factor) and plethysmography, before and after methacholine, to assess airway obstruction (AO) and airway hyperreactivity (AHR). IL-12 (p35) KO mice infected with M. pneumoniae were found to have significantly lower BAL M. pneumoniae concentrations compared with M. pneumoniae-infected WT mice. Lung HPS and the parenchymal pneumonia subscores (neutrophilic alveolar infiltrate), as well as AO, were significantly lower in infected KO mice. No difference was found for AHR. Infected KO mice had significantly lower BAL concentrations of IFN-gamma than WT mice; a trend toward lower BAL concentrations was observed for IL-10 (P = 0.065) and TNF-alpha (P = 0.078). No differences were found for IL-1beta, IL-2, IL-4, IL-5, or IL-6. The lack of IL-12 in experimental M. pneumoniae pneumonia was associated with less severe pulmonary disease and more rapid microbiologic and histologic resolution.
肺炎支原体是肺炎的主要病因,且与哮喘有关。有证据表明肺炎支原体呼吸道疾病的严重程度与呼吸道分泌物中的白细胞介素-12(IL-12)浓度有关。我们评估了白细胞介素-12(p35)基因敲除(KO)小鼠和野生型(WT)小鼠中肺炎支原体肺炎的微生物学、炎症和肺功能指标,以确定IL-12在肺炎支原体呼吸道疾病中的作用。8周龄的野生型BALB/c小鼠和8周龄的IL-12(p35)基因敲除BALB/c小鼠经鼻内接种10⁷CFU的肺炎支原体一次。在接种后第2、4和7天对小鼠进行评估。结果变量包括支气管肺泡灌洗(BAL)液中肺炎支原体的定量培养、肺组织病理学评分(HPS)、通过酶联免疫吸附测定法测定的BAL细胞因子浓度(肿瘤坏死因子α [TNF-α]、γ干扰素 [IFN-γ]、IL-1β、IL-2、IL-4、IL-5、IL-6、IL-10和粒细胞-巨噬细胞集落刺激因子)以及在乙酰甲胆碱前后进行体积描记法,以评估气道阻塞(AO)和气道高反应性(AHR)。发现感染肺炎支原体的IL-12(p35)基因敲除小鼠的BAL液中肺炎支原体浓度显著低于感染肺炎支原体的野生型小鼠。感染的基因敲除小鼠的肺HPS以及实质肺炎亚评分(嗜中性粒细胞肺泡浸润)和AO均显著较低。未发现AHR有差异。感染的基因敲除小鼠的BAL液中IFN-γ浓度显著低于野生型小鼠;观察到IL-10(P = 0.065)和TNF-α(P = 0.078)的BAL液浓度有降低趋势。IL-1β、IL-2、IL-4、IL-5或IL-6未发现差异。实验性肺炎支原体肺炎中缺乏IL-12与较轻的肺部疾病以及更快的微生物学和组织学缓解相关。