Department of Biochemistry and Immunology, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Department of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
J Appl Microbiol. 2021 Jun;130(6):2075-2086. doi: 10.1111/jam.14913. Epub 2020 Nov 22.
Allergic asthma is a chronic inflammatory lung disease characterized by a Th2-type immune response pattern. The development of nonspecific immunotherapy is one of the primary goals for the control of this disease.
In this study, we evaluated the therapeutic effects of Lactococcus lactis-producing mycobacterial heat shock protein 65 (LLHsp65) in an ovalbumin (OVA)-induced allergic asthma model. OVA-challenged BALB/c mice were orally administrated with LLHsp65 for 10 consecutive days. The results demonstrate that LLhsp65 attenuates critical features of allergic inflammation, like airway hyperresponsiveness and mucus production. Likewise, the treatment decreases the pulmonary eosinophilia and the serum level of OVA-specific IgE. In addition to deviating immune responses towards Th1-cytokine profile, increase regulatory T cells, and cytokine levels, such as IL-6 and IL-10.
Our results reveal that the mucosal immunotherapy of LLHsp65 significantly reduces the overall burden of airway allergic inflammation, suggesting a promising therapeutic strategy for allergic asthma treatment.
This research reveals new perspectives on nonspecific immunotherapy based on the delivery of recombinant proteins by lactic acid bacteria to treat of allergic disorders.
过敏性哮喘是一种慢性炎症性肺部疾病,其特征是 Th2 型免疫应答模式。非特异性免疫疗法的发展是控制这种疾病的主要目标之一。
在本研究中,我们评估了产分枝杆菌热休克蛋白 65 的乳酸乳球菌(LLHsp65)在卵清蛋白(OVA)诱导的过敏性哮喘模型中的治疗效果。用 OVA 挑战 BALB/c 小鼠,连续 10 天口服 LLHsp65。结果表明,LLhsp65 可减轻过敏性炎症的关键特征,如气道高反应性和黏液产生。同样,该治疗可减少肺嗜酸性粒细胞增多和 OVA 特异性 IgE 的血清水平。除了使免疫应答偏向 Th1 细胞因子谱、增加调节性 T 细胞和细胞因子水平(如 IL-6 和 IL-10)之外。
我们的结果表明,LLHsp65 的黏膜免疫疗法可显著减轻气道过敏性炎症的总体负担,为过敏性哮喘的治疗提供了一种有前途的治疗策略。
这项研究基于通过乳酸菌递送重组蛋白来治疗过敏疾病,为非特异性免疫疗法提供了新的视角。