Kim Byoung-Ju, Kwon Ji-Won, Seo Ju-Hee, Choi Won-Ah, Kim Young-Jun, Kang Mi-Jin, Yu Jinho, Hong Soo-Jong
Department of Pediatrics, Inje University College of Medicine, Busan, Korea.
Korean J Pediatr. 2011 Sep;54(9):373-9. doi: 10.3345/kjp.2011.54.9.373. Epub 2011 Sep 30.
4-1BB (CD 137) is a costimulatory molecule expressed on activated T-cells. Repression by 4-1BB is thought to attenuate Th2-mediated allergic reactions. The aim of this study was to investigate the effect of 4-1BB on allergic airway inflammation in a murine asthma model.
BALB/c mice were sensitized to and challenged with ovalbumin (OVA). Hu.4-1BB-Fc was administered 1 day before the first OVA sensitization or 1 day after the second OVA sensitization. Following antigen challenge, airway responsiveness to methacholine was assessed and bronchoalveolar lavage (BAL) fluid was analyzed. Total immunoglobulin (Ig) E, OVA-specific IgE, IgG(1), and IgG(2a) levels in sera were measured by enzyme-linked immunosorbent assay. Lung pathology was also evaluated.
In mice treated with Hu.4-1BB-Fc before the first OVA sensitization, there was a marked decrease in airway hyperresponsiveness, total cell count, and eosinophil count in the BAL fluid. In addition, Hu.4-1BB-Fc treatment decreased serum OVA-specific IgG(1) levels and increased serum IgG(2a) level significantly compared with the corresponding levels in mice sensitized to and challenged with OVA. Hu.4-1BB-Fc-treated mice also showed suppressed peribronchial and perivascular inflammatory cell infiltration. In contrast, treatment with Hu.4-1BB-Fc 1 day after sensitization had no effect on airway hyperresponsiveness and showed less suppression of inflammation in lung tissue.
Administration of Hu.4-1BB-Fc can attenuate airway inflammation and hyperreactivity in a mouse model of allergic airway inflammation. In addition, administration before sensitization may be more effective. These findings suggest that 4-1BB may be a useful therapeutic molecule against asthma.
4-1BB(CD137)是一种在活化T细胞上表达的共刺激分子。4-1BB的抑制作用被认为可减弱Th2介导的过敏反应。本研究旨在探讨4-1BB对小鼠哮喘模型中过敏性气道炎症的影响。
用卵清蛋白(OVA)对BALB/c小鼠进行致敏和激发。在首次OVA致敏前1天或第二次OVA致敏后1天给予Hu.4-1BB-Fc。抗原激发后,评估气道对乙酰甲胆碱的反应性,并分析支气管肺泡灌洗(BAL)液。通过酶联免疫吸附测定法测量血清中的总免疫球蛋白(Ig)E、OVA特异性IgE、IgG(1)和IgG(2a)水平。还评估了肺病理学。
在首次OVA致敏前用Hu.4-1BB-Fc治疗的小鼠中,气道高反应性、BAL液中的总细胞计数和嗜酸性粒细胞计数显著降低。此外,与OVA致敏和激发的小鼠的相应水平相比,Hu.4-1BB-Fc治疗显著降低了血清OVA特异性IgG(1)水平并提高了血清IgG(2a)水平。Hu.4-1BB-Fc治疗的小鼠还表现出支气管周围和血管周围炎症细胞浸润受到抑制。相比之下,致敏后1天用Hu.4-1BB-Fc治疗对气道高反应性没有影响,并且对肺组织炎症的抑制作用较小。
给予Hu.4-1BB-Fc可减轻过敏性气道炎症小鼠模型中的气道炎症和高反应性。此外,致敏前给药可能更有效。这些发现表明4-1BB可能是一种治疗哮喘的有用治疗分子。