{"title":"益生元对特应性皮炎的影响。","authors":"Kangmo Ahn","doi":"10.4168/aair.2023.15.3.271","DOIUrl":null,"url":null,"abstract":"https://e-aair.org The human microbiota interacts with host immunity, leading to immune dysfunction associated with allergy and asthma.1 In particular, many studies revealed that gut microbiota plays an important role in the pathophysiology of atopic dermatitis (AD). In a comparative analysis between AD patients and healthy controls, the former group showed diminished levels of Bifidobacterium in the gut. Furthermore, an inverse correlation was identified between AD severity and percentages of Bifidobacterium.2 Low gut microbiota diversity (P = 0.004), particularly low diversity of the bacterial phylum Bacteroidetes (P = 0.02) and the genus Bacteroides (P = 0.01), at 1 month of age was significantly associated with AD until 2 years of age.3 When compared to the control group, a subgroup of AD showed lower functional genes related to host immune development and this finding was associated with reduced colonization of mucin-degrading bacteria (Akkermansia muciniphila, Ruminococcus gnavus, and Lachnospiraceae bacterium 2_1_58FAA) in the gut.4 The fecal samples at 6 months of age showed that the proportion of Streptococcus was significantly higher and Clostridium was significantly lower In infants with AD at 2 years of age.5 Overall, the development and persistence of AD are associated with alterations in the gut microbiome, and this effect may be mediated by the gutskin axis through immunologic, metabolic, and neuroendocrine pathways.6,7","PeriodicalId":7547,"journal":{"name":"Allergy, Asthma & Immunology Research","volume":"15 3","pages":"271-275"},"PeriodicalIF":4.1000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3a/f9/aair-15-271.PMC10186120.pdf","citationCount":"2","resultStr":"{\"title\":\"The Effect of Prebiotics on Atopic Dermatitis.\",\"authors\":\"Kangmo Ahn\",\"doi\":\"10.4168/aair.2023.15.3.271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"https://e-aair.org The human microbiota interacts with host immunity, leading to immune dysfunction associated with allergy and asthma.1 In particular, many studies revealed that gut microbiota plays an important role in the pathophysiology of atopic dermatitis (AD). In a comparative analysis between AD patients and healthy controls, the former group showed diminished levels of Bifidobacterium in the gut. Furthermore, an inverse correlation was identified between AD severity and percentages of Bifidobacterium.2 Low gut microbiota diversity (P = 0.004), particularly low diversity of the bacterial phylum Bacteroidetes (P = 0.02) and the genus Bacteroides (P = 0.01), at 1 month of age was significantly associated with AD until 2 years of age.3 When compared to the control group, a subgroup of AD showed lower functional genes related to host immune development and this finding was associated with reduced colonization of mucin-degrading bacteria (Akkermansia muciniphila, Ruminococcus gnavus, and Lachnospiraceae bacterium 2_1_58FAA) in the gut.4 The fecal samples at 6 months of age showed that the proportion of Streptococcus was significantly higher and Clostridium was significantly lower In infants with AD at 2 years of age.5 Overall, the development and persistence of AD are associated with alterations in the gut microbiome, and this effect may be mediated by the gutskin axis through immunologic, metabolic, and neuroendocrine pathways.6,7\",\"PeriodicalId\":7547,\"journal\":{\"name\":\"Allergy, Asthma & Immunology Research\",\"volume\":\"15 3\",\"pages\":\"271-275\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3a/f9/aair-15-271.PMC10186120.pdf\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Allergy, Asthma & Immunology Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.4168/aair.2023.15.3.271\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ALLERGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Allergy, Asthma & Immunology Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4168/aair.2023.15.3.271","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
https://e-aair.org The human microbiota interacts with host immunity, leading to immune dysfunction associated with allergy and asthma.1 In particular, many studies revealed that gut microbiota plays an important role in the pathophysiology of atopic dermatitis (AD). In a comparative analysis between AD patients and healthy controls, the former group showed diminished levels of Bifidobacterium in the gut. Furthermore, an inverse correlation was identified between AD severity and percentages of Bifidobacterium.2 Low gut microbiota diversity (P = 0.004), particularly low diversity of the bacterial phylum Bacteroidetes (P = 0.02) and the genus Bacteroides (P = 0.01), at 1 month of age was significantly associated with AD until 2 years of age.3 When compared to the control group, a subgroup of AD showed lower functional genes related to host immune development and this finding was associated with reduced colonization of mucin-degrading bacteria (Akkermansia muciniphila, Ruminococcus gnavus, and Lachnospiraceae bacterium 2_1_58FAA) in the gut.4 The fecal samples at 6 months of age showed that the proportion of Streptococcus was significantly higher and Clostridium was significantly lower In infants with AD at 2 years of age.5 Overall, the development and persistence of AD are associated with alterations in the gut microbiome, and this effect may be mediated by the gutskin axis through immunologic, metabolic, and neuroendocrine pathways.6,7
期刊介绍:
The journal features cutting-edge original research, brief communications, and state-of-the-art reviews in the specialties of allergy, asthma, and immunology, including clinical and experimental studies and instructive case reports. Contemporary reviews summarize information on topics for researchers and physicians in the fields of allergy and immunology. As of January 2017, AAIR do not accept case reports. However, if it is a clinically important case, authors can submit it in the form of letter to the Editor. Editorials and letters to the Editor explore controversial issues and encourage further discussion among physicians dealing with allergy, immunology, pediatric respirology, and related medical fields. AAIR also features topics in practice and management and recent advances in equipment and techniques for clinicians concerned with clinical manifestations of allergies and pediatric respiratory diseases.