{"title":"芽孢杆菌中的中性粒细胞活化蛋白通过 TLR2 信号传导抑制酪蛋白过敏。","authors":"Zhuwei Liang, Chao Zhang, Xiaoyu Liu, Kaiyue Yang, Zhile Xiong, Bingshao Liang, Jialiang Mai, Xiaojun Xiao, Jie Liu, Pingchang Yang, Damo Xu, Zhenwen Zhou","doi":"10.3389/fimmu.2024.1428079","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Milk allergy commonly occurs in children, mainly caused by bovine-derived casein (CAS) protein. Neutrophil-activating protein (NAP) of <i>Helicobacter pylori</i> plays an immunomodulatory role with potential to suppress Th2-type immune responses. <i>Bacillus subtilis</i> (<i>B. subtilis</i>) spores are commonly used as oral vectors for drug delivery.</p><p><strong>Objective: </strong>To investigate whether recombinantly expressed NAP on <i>B. subtilis</i> spores could be an effective treatment for CAS allergy in mouse.</p><p><strong>Methods: </strong>After CAS sensitization, mice were orally administered <i>B. subtilis</i> spores expressing recombinant NAP for 6 weeks. Allergic symptoms and parameters were evaluated after CAS challenge oral gavage, including allergic inflammation, splenic cytokines, and serum-specific antibodies. Protein levels of Toll-like receptor 2 (TLR2) and c-JUN in the jejunum tissue were measured by western blot. Bone marrow-derived macrophages (BMDMs) were stimulated with inactivated NAP spores to measure the influence on cytokine profiles <i>in vitro</i>.</p><p><strong>Results: </strong>NAP recombinant spore treatment significantly reduced allergic symptoms and intestinal inflammation. Interleukin-12 and interferon-gamma levels increased, whereas serum CAS-specific IgG1 and IgE levels decreased. TLR2 and c-JUN expression levels were elevated in the jejunal tissue. Inactivated NAP spores polarized BMDMs to the M1 phenotype and enhanced cytokine expression, which were inhibited by a TLR2 neutralizing antibody.</p><p><strong>Conclusion: </strong>NAP offers a new strategy in the treatment of CAS allergy by inhibiting the Th2 response, while eliciting macrophages to promote Th1 immune responses.</p>","PeriodicalId":12622,"journal":{"name":"Frontiers in Immunology","volume":"15 ","pages":"1428079"},"PeriodicalIF":5.7000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11574345/pdf/","citationCount":"0","resultStr":"{\"title\":\"Neutrophil-activating protein in <i>Bacillus</i> spores inhibits casein allergy via TLR2 signaling.\",\"authors\":\"Zhuwei Liang, Chao Zhang, Xiaoyu Liu, Kaiyue Yang, Zhile Xiong, Bingshao Liang, Jialiang Mai, Xiaojun Xiao, Jie Liu, Pingchang Yang, Damo Xu, Zhenwen Zhou\",\"doi\":\"10.3389/fimmu.2024.1428079\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Milk allergy commonly occurs in children, mainly caused by bovine-derived casein (CAS) protein. Neutrophil-activating protein (NAP) of <i>Helicobacter pylori</i> plays an immunomodulatory role with potential to suppress Th2-type immune responses. <i>Bacillus subtilis</i> (<i>B. subtilis</i>) spores are commonly used as oral vectors for drug delivery.</p><p><strong>Objective: </strong>To investigate whether recombinantly expressed NAP on <i>B. subtilis</i> spores could be an effective treatment for CAS allergy in mouse.</p><p><strong>Methods: </strong>After CAS sensitization, mice were orally administered <i>B. subtilis</i> spores expressing recombinant NAP for 6 weeks. Allergic symptoms and parameters were evaluated after CAS challenge oral gavage, including allergic inflammation, splenic cytokines, and serum-specific antibodies. Protein levels of Toll-like receptor 2 (TLR2) and c-JUN in the jejunum tissue were measured by western blot. Bone marrow-derived macrophages (BMDMs) were stimulated with inactivated NAP spores to measure the influence on cytokine profiles <i>in vitro</i>.</p><p><strong>Results: </strong>NAP recombinant spore treatment significantly reduced allergic symptoms and intestinal inflammation. Interleukin-12 and interferon-gamma levels increased, whereas serum CAS-specific IgG1 and IgE levels decreased. TLR2 and c-JUN expression levels were elevated in the jejunal tissue. Inactivated NAP spores polarized BMDMs to the M1 phenotype and enhanced cytokine expression, which were inhibited by a TLR2 neutralizing antibody.</p><p><strong>Conclusion: </strong>NAP offers a new strategy in the treatment of CAS allergy by inhibiting the Th2 response, while eliciting macrophages to promote Th1 immune responses.</p>\",\"PeriodicalId\":12622,\"journal\":{\"name\":\"Frontiers in Immunology\",\"volume\":\"15 \",\"pages\":\"1428079\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11574345/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/fimmu.2024.1428079\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fimmu.2024.1428079","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:牛奶过敏常见于儿童,主要由牛源性酪蛋白(CAS)引起。幽门螺杆菌的中性粒细胞活化蛋白(NAP)具有免疫调节作用,可抑制 Th2 型免疫反应。枯草芽孢杆菌(B.subtilis)孢子通常用作口服给药载体:目的:研究在枯草芽孢杆菌孢子上重组表达的 NAP 能否有效治疗小鼠对 CAS 的过敏:方法:CAS致敏后,给小鼠口服表达重组 NAP 的枯草芽孢 6 周。方法:CAS致敏后,给小鼠口服表达重组NAP的枯草芽孢杆菌孢子,持续6周。口服CAS后,对小鼠的过敏症状和参数进行评估,包括过敏性炎症、脾细胞因子和血清特异性抗体。空肠组织中Toll样受体2(TLR2)和c-JUN的蛋白水平通过Western印迹法进行了测定。用灭活的 NAP 孢子刺激骨髓衍生巨噬细胞(BMDMs),测量其对体外细胞因子谱的影响:结果:NAP 重组孢子处理可明显减轻过敏症状和肠道炎症。白细胞介素-12和γ干扰素水平升高,而血清CAS特异性IgG1和IgE水平下降。空肠组织中的 TLR2 和 c-JUN 表达水平升高。灭活的 NAP 孢子可将 BMDMs 极化为 M1 表型并增强细胞因子的表达,TLR2 中和抗体可抑制细胞因子的表达:结论:NAP 通过抑制 Th2 反应,同时激发巨噬细胞促进 Th1 免疫反应,为治疗 CAS 过敏症提供了一种新策略。
Neutrophil-activating protein in Bacillus spores inhibits casein allergy via TLR2 signaling.
Background: Milk allergy commonly occurs in children, mainly caused by bovine-derived casein (CAS) protein. Neutrophil-activating protein (NAP) of Helicobacter pylori plays an immunomodulatory role with potential to suppress Th2-type immune responses. Bacillus subtilis (B. subtilis) spores are commonly used as oral vectors for drug delivery.
Objective: To investigate whether recombinantly expressed NAP on B. subtilis spores could be an effective treatment for CAS allergy in mouse.
Methods: After CAS sensitization, mice were orally administered B. subtilis spores expressing recombinant NAP for 6 weeks. Allergic symptoms and parameters were evaluated after CAS challenge oral gavage, including allergic inflammation, splenic cytokines, and serum-specific antibodies. Protein levels of Toll-like receptor 2 (TLR2) and c-JUN in the jejunum tissue were measured by western blot. Bone marrow-derived macrophages (BMDMs) were stimulated with inactivated NAP spores to measure the influence on cytokine profiles in vitro.
Results: NAP recombinant spore treatment significantly reduced allergic symptoms and intestinal inflammation. Interleukin-12 and interferon-gamma levels increased, whereas serum CAS-specific IgG1 and IgE levels decreased. TLR2 and c-JUN expression levels were elevated in the jejunal tissue. Inactivated NAP spores polarized BMDMs to the M1 phenotype and enhanced cytokine expression, which were inhibited by a TLR2 neutralizing antibody.
Conclusion: NAP offers a new strategy in the treatment of CAS allergy by inhibiting the Th2 response, while eliciting macrophages to promote Th1 immune responses.
期刊介绍:
Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.