由新分离的产乳酸菌株组成的合成菌对小鼠过敏性哮喘的免疫调节作用

IF 3.7 4区 医学 Q2 CELL BIOLOGY
Naina Monga , Shikha Sharma , Ruchika Bhatia , Mahendra Bishnoi , Kanthi Kiran Kondepudi , Amarjit S. Naura
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引用次数: 0

摘要

鉴于肠道微生物群在哮喘发病中的作用,本研究采用基于卵清蛋白(OVA)的小鼠模型,评估新分离的产乳酸菌株短双歧杆菌Bif11和植物乳杆菌LAB31对哮喘的免疫调节作用。我们的研究结果表明,这两种菌株都可能通过产生短链脂肪酸(SCFAs)来调节Th2免疫反应,从而抑制ova诱导的气道炎症。此外,由菌株和益生元组成的低聚异麦芽糖通过改善Th2免疫反应的调节,在改善ova诱导的气道炎症方面表现出优异的潜力。此外,合成物还可以防止ova诱导的粘液过量产生和气道高反应性。这种保护与肠道微生物群的正常化和盲肠中scfa的增加有关,而scfa的产生与脾脏中t调节细胞的数量密切相关。总的来说,我们的新型合成物具有微调免疫反应的能力,为过敏性哮喘提供保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunomodulatory action of synbiotic comprising of newly isolated lactic acid producing bacterial strains against allergic asthma in mice

Given the reported role of gut-microbiota in asthma pathogenesis, the present work was carried to evaluate immunomodulatory action of newly isolated lactic acid producing bacterial strains Bifidobacterium breve Bif11 and Lactiplantibacillus plantarum LAB31 against asthma using ovalbumin (OVA) based mouse model. Our results show that both strains modulate Th2 immune response potentially through production of short chain fatty acids (SCFAs), resulting in suppression of OVA-induced airway inflammation. Furthermore, synbiotic comprising of both strains and prebiotic, Isomaltooligosaccharide exhibited superior potential in amelioration of OVA-induced airway inflammation through improved modulation of Th2 immune response. Further, synbiotic protects against OVA-induced mucus hyper-production and airway-hyperresponsiveness. Such protection was associated with normalization of gut microbiome and enhanced production of SCFAs in cecum which correlates closely with population of T-regulatory cells in spleen. Overall, our novel synbiotic possesses the ability to fine-tune the immune response for providing protection against allergic asthma.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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