Tripathi Prabhanshu, Kukreja Neetu, Singh B P, Arora Naveen
Allergy and Immunology Section, Institute of Genomics and Integrative Biology, D.U. North Campus, Mall Road, Delhi 110 007, India.
J Clin Immunol. 2009 May;29(3):292-302. doi: 10.1007/s10875-008-9261-9. Epub 2008 Nov 20.
Studies with mite allergens demonstrated that proteolytic activity augments allergic airway inflammation. This knowledge is limited to few enzyme allergens.
The objective of this study is to investigate the effect of serine protease Cur l 1 from Curvularia lunata in airway inflammation/hyper-responsiveness.
Cur l 1 was purified and inactivated using a serine protease inhibitor. Balb/c mice were sensitized with enzymatically active Cur l 1 or C. lunata extract. Sensitized mice were given booster dose on day 14 with active or inactivated Cur l 1. Intranasal challenge was given on day 28, 29, and 30. Airway hyper-responsiveness was measured by plethysmography. Blood, bronchoalveolar lavage fluid (BALF), spleen, and lungs from mice were analyzed for cellular infiltration, immunoglobulins, and cytokine levels.
Mice challenged with enzymatically active Cur l 1 demonstrated significantly higher airway inflammation than inactive Cur l 1 group mice (p < 0.01). There was a significant difference in serum IgE and IgG1 levels among mice immunized with active Cur l 1 and inactive Cur l 1 (p < 0.01). IL-4 and IL-5 were higher in BALF and splenocyte culture supernatant of active Cur l 1 than inactive Cur l 1 mice. Lung histology revealed increased eosinophil infiltration, goblet cell hyperplasia and mucus secretion in active group.
Proteolytic activity of Cur l 1 plays an important role in airway inflammation and the inactivated Cur l 1 has potential to be explored for immunotherapy.
对螨过敏原的研究表明,蛋白水解活性会加剧过敏性气道炎症。这一认识仅限于少数几种酶过敏原。
本研究的目的是调查来自新月弯孢霉的丝氨酸蛋白酶Cur l 1在气道炎症/高反应性中的作用。
使用丝氨酸蛋白酶抑制剂对Cur l 1进行纯化和灭活。用具有酶活性的Cur l 1或新月弯孢霉提取物对Balb/c小鼠进行致敏。在第14天用活性或灭活的Cur l 1对致敏小鼠进行加强剂量注射。在第28、29和30天进行鼻内激发。通过体积描记法测量气道高反应性。对小鼠的血液、支气管肺泡灌洗液(BALF)、脾脏和肺进行细胞浸润、免疫球蛋白和细胞因子水平分析。
用具有酶活性的Cur l 1激发的小鼠表现出比灭活的Cur l 1组小鼠明显更高的气道炎症(p < 0.01)。在用活性Cur l 1和灭活的Cur l 1免疫的小鼠之间,血清IgE和IgG1水平存在显著差异(p < 0.01)。活性Cur l 1组小鼠的BALF和脾细胞培养上清液中的IL-4和IL-5高于灭活的Cur l 1组小鼠。肺组织学显示,活性组中嗜酸性粒细胞浸润增加、杯状细胞增生和黏液分泌增多。
Cur l 1的蛋白水解活性在气道炎症中起重要作用,灭活的Cur l 1有用于免疫治疗的潜在研究价值。