Dawson Harry, Solano-Aguilar Gloria, Beal Madeline, Beshah Ethiopia, Vangimalla Vandana, Jones Eudora, Botero Sebastian, Urban Joseph F
Diet, Genomics, & Immunology Laboratory, Beltsville Human Nutrition Research Center, U.S. Department of Agriculture, Beltsville, MD 20705, USA.
Infect Immun. 2009 Jun;77(6):2576-87. doi: 10.1128/IAI.00827-07. Epub 2009 Mar 30.
Pigs infected with Ascaris suum or controls were given 100 microg (low-dose) or 1,000 microg (high-dose) all-trans retinoic acid (ATRA)/kg body weight in corn oil or corn oil alone per os on days after inoculation (DAI) -1, +1, and +3 with infective eggs. Treatment with ATRA increased interleukin 4 (IL4) and IL12p70 in plasma of infected pigs at 7 DAI and augmented bronchoalveolar lavage (BAL) eosinophilia observed at 7 and 14 DAI. To explore potential molecular mechanisms underlying these observations, a quantitative real-time reverse transcription (RT)-PCR array was used to examine mRNA expression in tissue. Ascaris-infected pigs had increased levels of liver mRNA for T-helper-2 (Th2)-associated cytokines, mast cell markers, and T regulatory (Treg) cells, while infected pigs given ATRA had higher IL4, IL13, CCL11, CCL26, CCL17, CCL22, and TPSB1 expression. Gene expression for Th1-associated markers (IFNG, IL12B, and TBX21), the CXCR3 ligand (CXCL9), IL1B, and the putative Treg marker TNFRSF18 was also increased. Expression of IL4, IL13, IL1B, IL6, CCL11, and CCL26 was increased in the lungs of infected pigs treated with ATRA. To determine a putative cellular source of eosinophil chemoattractants, alveolar macrophages were treated with IL4 and/or ATRA in vitro. IL4 induced CCL11, CCL17, CCL22, and CCL26 mRNA, and ATRA increased the basal and IL4-stimulated expression of CCL17 and CCL22. Thus, ATRA augments a diverse Th1-, Th2-, Treg-, and inflammation-associated response in swine infected with A. suum, and the increased BAL eosinophilia may be related to enhanced induction of eosinophil chemokine activity by alveolar macrophages.
给感染猪蛔虫的猪或对照猪在接种感染性虫卵后的第-1、+1和+3天,经口给予100微克(低剂量)或1000微克(高剂量)的全反式维甲酸(ATRA)/千克体重,溶剂为玉米油或仅为玉米油。在感染后第7天,用ATRA治疗可增加感染猪血浆中的白细胞介素4(IL4)和IL12p70,并增强在感染后第7天和第14天观察到的支气管肺泡灌洗(BAL)嗜酸性粒细胞增多。为了探究这些观察结果背后的潜在分子机制,使用定量实时逆转录(RT)-PCR阵列检测组织中的mRNA表达。感染猪蛔虫的猪肝脏中与辅助性T细胞2(Th2)相关的细胞因子、肥大细胞标志物和调节性T(Treg)细胞的mRNA水平升高,而给予ATRA的感染猪IL4、IL13、CCL11、CCL26、CCL17、CCL22和TPSB1的表达更高。与Th1相关的标志物(IFNG、IL12B和TBX21)、CXCR3配体(CXCL9)、IL1B和假定的Treg标志物TNFRSF18的基因表达也增加。在用ATRA治疗的感染猪的肺中,IL4、IL13、IL1B、IL6、CCL11和CCL26的表达增加。为了确定嗜酸性粒细胞趋化因子的假定细胞来源,体外将肺泡巨噬细胞用IL4和/或ATRA处理。IL4诱导CCL11、CCL17、CCL22和CCL26 mRNA表达,而ATRA增加CCL17和CCL22的基础表达以及IL4刺激的表达。因此,ATRA增强了感染猪蛔虫的猪体内多种与Th1、Th2、Treg和炎症相关的反应,BAL嗜酸性粒细胞增多可能与肺泡巨噬细胞增强嗜酸性粒细胞趋化因子活性的诱导有关。