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弓形虫丝氨酸蛋白酶抑制剂-1:一种用于哮喘治疗的新型佐剂候选物。

Toxoplasma gondii serine-protease inhibitor-1: A new adjuvant candidate for asthma therapy.

作者信息

Soto Ariadna S, Fenoy Ignacio M, Sanchez Vanesa R, March Florencia, Perrone Sibilia Matías D, Aldirico María de Los Angeles, Picchio Mariano S, Arcon Nadia, Acosta Patricio L, Polack Fernando P, Martin Valentina, Goldman Alejandra

机构信息

Laboratorio de Inmunología, Vacunas y Alergia, CESyMA, Escuela de Ciencia y Tecnología, Universidad Nacional de San Martín, Buenos Aires, Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.

出版信息

PLoS One. 2017 Oct 26;12(10):e0187002. doi: 10.1371/journal.pone.0187002. eCollection 2017.

Abstract

Serine-proteases are important players in the pathogenesis of asthma, promoting inflammation and tissue remodeling. It's also known that many serine protease inhibitors display immunomodulatory properties. TgPI-1 is a Toxoplasma gondii protein that exhibits broad spectrum inhibitory activity against serine proteases. In view of the increased prevalence of atopic disorders and the need to develop new treatment strategies we sought to investigate the potential of TgPI-1 for treating respiratory allergies. For this purpose, we developed a therapeutic experimental model. BALB/c mice were rendered allergic by intraperitoneal ovalbumin-alum sensitization and airway-challenged. Once the asthmatic phenotype was achieved, mice were intranasally treated with rTgPI-1 alone or with a mixture of rTgPI-1 and ovalbumin (OVA). A week later mice were given a secondary aerosol challenge. Treatment with rTgPI-1 alone or co-administered with OVA diminished bronchoalveolar eosinophilia, mucus production and peribronchial lung infiltration. This effect was accompanied by a lung resistance reduction of 26.3% and 50.3% respectively. Both treatments resulted in the production of lower levels of IL-4, IL-5, IFN-γ and regulatory IL-10 by thoracic lymph node cells stimulated with OVA. Interestingly, significant decreases in OVA specific IgE and T cell proliferation, and increases in FoxP3+ T cells at local and systemic levels were only detected when the inhibitor was administered along with OVA. These results show that both rTgPI-1 treatments reduced asthma hallmarks. However, co-administration of the inhibitor with the allergen was more effective. Hence, rTgPI-1 emerges as a novel adjuvant candidate for asthma treatment.

摘要

丝氨酸蛋白酶是哮喘发病机制中的重要参与者,可促进炎症和组织重塑。还已知许多丝氨酸蛋白酶抑制剂具有免疫调节特性。TgPI-1是一种弓形虫蛋白,对丝氨酸蛋白酶具有广谱抑制活性。鉴于特应性疾病的患病率增加以及开发新治疗策略的必要性,我们试图研究TgPI-1治疗呼吸道过敏的潜力。为此,我们建立了一个治疗性实验模型。通过腹腔注射卵清蛋白-明矾致敏和气道激发使BALB/c小鼠过敏。一旦达到哮喘表型,小鼠分别经鼻单独用rTgPI-1或用rTgPI-1与卵清蛋白(OVA)的混合物进行治疗。一周后,对小鼠进行二次气雾剂激发。单独用rTgPI-1治疗或与OVA联合给药可减少支气管肺泡嗜酸性粒细胞增多、黏液分泌和支气管周围肺浸润。这种作用分别伴随着肺阻力降低26.3%和50.3%。两种治疗均导致OVA刺激的胸段淋巴结细胞产生较低水平的IL-4、IL-5、IFN-γ和调节性IL-10。有趣的是,仅当抑制剂与OVA一起给药时,才检测到OVA特异性IgE和T细胞增殖显著降低,以及局部和全身水平的FoxP3+ T细胞增加。这些结果表明,两种rTgPI-1治疗均降低了哮喘的特征。然而,抑制剂与变应原联合给药更有效。因此,rTgPI-1成为一种新型的哮喘治疗佐剂候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a0f/5658115/c68bdb8283e9/pone.0187002.g001.jpg

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