Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Immunol Lett. 2010 May 4;130(1-2):97-106. doi: 10.1016/j.imlet.2009.12.006. Epub 2009 Dec 11.
Hyper IgE Syndrome (HIES) is a rare genetic disorder, characterized by elevated serum IgE levels and reduced inflammatory responses to bacterial infections. This leads to dermatitis, recurrent lung infections and "cold abscesses". Recently, progress was made in HIES research, when mutations in STAT3 were found in the autosomal dominant form of HIES, and impaired responses of T helper 17 cells were reported. However, the causes for reduced inflammatory responses in these patients were not fully elucidated. In view of studies that indicated that polymorphonuclear leukocytes (PMN) of HIES patients are defective in their chemotactic properties, we asked if the PMN of these patients have reduced expression of receptors for chemoattractants. To analyze this possibility, we focused on fMLP and ELR(+)-CXC chemokines - which are essential for mounting acute inflammatory responses - and determined the coding sequences and expression levels of their corresponding receptors: FPR (for fMLP) as well as CXCR1 and CXCR2 (the receptors for ELR(+)-CXC chemokines). The analyses of these receptors in HIES patients indicated that their coding sequences were intact and normal. However, the percentages of PMN that expressed FPR, CXCR1 and CXCR2 were significantly lower in HIES patients. In addition, lower expression levels per cell were denoted for CXCR1 in PMN of the patients. A cumulative score that was calculated for the three chemoattractant receptors together indicated that in some of the patients there were prominent reductions, of up to approximately 50% in the overall expression of the receptors (indicated by % positive cells and mean expression levels per cell). In addition, we asked whether deregulation of PMN activities in HIES may result from binding of IgE to corresponding receptors on HIES PMN. Our findings indicate that this is probably not the case, because similarly to normal PMN, the cells of HIES patients did not express notable levels of the IgE receptors FcvarepsilonRI and FcvarepsilonRII. Together, these results provide novel information on the expression of key determinants in PMN migration in HIES, suggesting that a defect in the expression of chemoattractant receptors may lead to impaired chemotaxis found in HIES patients, and to decreased inflammatory responses.
高免疫球蛋白 E 综合征(HIES)是一种罕见的遗传性疾病,其特征是血清 IgE 水平升高和对细菌感染的炎症反应降低。这导致了皮炎、复发性肺部感染和“寒性脓肿”。最近,在 HIES 研究方面取得了进展,发现常染色体显性遗传形式的 HIES 存在 STAT3 突变,并报道了辅助性 T 细胞 17 细胞反应受损。然而,这些患者炎症反应降低的原因尚未完全阐明。鉴于研究表明 HIES 患者的多形核白细胞(PMN)在趋化性方面存在缺陷,我们询问这些患者的 PMN 是否表达降低了趋化因子受体。为了分析这种可能性,我们专注于 fMLP 和 ELR(+)-CXC 趋化因子——这对于引发急性炎症反应至关重要——并确定了它们相应受体的编码序列和表达水平:fMLP 的 FPR 受体以及 ELR(+)-CXC 趋化因子的 CXCR1 和 CXCR2 受体。对 HIES 患者这些受体的分析表明,它们的编码序列完整且正常。然而,HIES 患者的 PMN 表达 FPR、CXCR1 和 CXCR2 的百分比明显较低。此外,患者 PMN 中的 CXCR1 每个细胞的表达水平也较低。对这三种趋化因子受体进行的累积评分表明,在一些患者中,受体的整体表达明显降低,约降低 50%(通过阳性细胞百分比和每个细胞的平均表达水平表示)。此外,我们还询问了 HIES 中 PMN 活性的失调是否可能是由于 IgE 与 HIES PMN 上相应受体结合所致。我们的研究结果表明,这可能不是这种情况,因为与正常 PMN 一样,HIES 患者的细胞也没有表达显著水平的 IgE 受体 FcεRI 和 FcεRII。综上所述,这些结果为 HIES 中 PMN 迁移的关键决定因素的表达提供了新的信息,表明趋化因子受体表达缺陷可能导致 HIES 患者的趋化作用受损,并导致炎症反应降低。