Abish S. Stephen, Stacy Worrall, Cheryl Somani, Robert P. Allaker, Janet Davies, Luigi Nibali, Nikolaos Donos
{"title":"非手术牙周治疗调节原发性免疫缺陷儿童的口腔微生物组。","authors":"Abish S. Stephen, Stacy Worrall, Cheryl Somani, Robert P. Allaker, Janet Davies, Luigi Nibali, Nikolaos Donos","doi":"10.1111/jcpe.14201","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background and Aim</h3>\n \n <p>Primary Immunodeficiencies (PIDs) arise from rare genetic defects affecting humoral and cellular immunity, which can lead to reduced dental plaque control. This study aimed to characterise the subgingival dental plaque microbiome in neutropenic PID children compared to healthy controls and assess their response to non-surgical periodontal therapy.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Subgingival plaque was collected from three first molars and one first incisor at baseline and 6 months post therapy from children with PID (<i>n</i> = 24) and systematically healthy control participants (<i>n</i> = 24) who were recruited from Great Ormond Street Hospital and Barts Health NHS Trust, respectively. The subgingival microbiome was profiled using an Illumina metabarcoding approach on the bacterial 16S rRNA gene V1–V2 region.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Significant shifts in community structure were observed post therapy, as measured by alpha and beta diversities. An increase in <i>Rothia</i> spp., <i>Neisseria</i> spp. and <i>Actinomyces</i> spp. was noted in PID children post therapy, consistent with clinical improvements. Baseline blood absolute neutrophil counts in PID children were positively associated with \n <i>Streptococcus cristatus</i>\n and <i>Gemella</i> spp., and negatively with <i>Saccharibacteria, Capnocytophaga</i> and <i>Porphyromonas</i> spp., highlighting key host–microbial relationships.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Non-surgical periodontal therapy modulated the subgingival microbiota in neutropenic PID children, revealing novel host–microbial interactions important for the oral microbiome in health.</p>\n </section>\n </div>","PeriodicalId":15380,"journal":{"name":"Journal of Clinical Periodontology","volume":"52 10","pages":"1410-1418"},"PeriodicalIF":6.8000,"publicationDate":"2025-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jcpe.14201","citationCount":"0","resultStr":"{\"title\":\"Non-Surgical Periodontal Therapy Modulates Oral Microbiome in Primary Immunodeficient Children\",\"authors\":\"Abish S. Stephen, Stacy Worrall, Cheryl Somani, Robert P. Allaker, Janet Davies, Luigi Nibali, Nikolaos Donos\",\"doi\":\"10.1111/jcpe.14201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background and Aim</h3>\\n \\n <p>Primary Immunodeficiencies (PIDs) arise from rare genetic defects affecting humoral and cellular immunity, which can lead to reduced dental plaque control. This study aimed to characterise the subgingival dental plaque microbiome in neutropenic PID children compared to healthy controls and assess their response to non-surgical periodontal therapy.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Subgingival plaque was collected from three first molars and one first incisor at baseline and 6 months post therapy from children with PID (<i>n</i> = 24) and systematically healthy control participants (<i>n</i> = 24) who were recruited from Great Ormond Street Hospital and Barts Health NHS Trust, respectively. The subgingival microbiome was profiled using an Illumina metabarcoding approach on the bacterial 16S rRNA gene V1–V2 region.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Significant shifts in community structure were observed post therapy, as measured by alpha and beta diversities. An increase in <i>Rothia</i> spp., <i>Neisseria</i> spp. and <i>Actinomyces</i> spp. was noted in PID children post therapy, consistent with clinical improvements. Baseline blood absolute neutrophil counts in PID children were positively associated with \\n <i>Streptococcus cristatus</i>\\n and <i>Gemella</i> spp., and negatively with <i>Saccharibacteria, Capnocytophaga</i> and <i>Porphyromonas</i> spp., highlighting key host–microbial relationships.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Non-surgical periodontal therapy modulated the subgingival microbiota in neutropenic PID children, revealing novel host–microbial interactions important for the oral microbiome in health.</p>\\n </section>\\n </div>\",\"PeriodicalId\":15380,\"journal\":{\"name\":\"Journal of Clinical Periodontology\",\"volume\":\"52 10\",\"pages\":\"1410-1418\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-07-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jcpe.14201\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Periodontology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jcpe.14201\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Periodontology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jcpe.14201","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
摘要
原发性免疫缺陷(pid)是由影响体液和细胞免疫的罕见遗传缺陷引起的,这可能导致对牙菌斑的控制减少。本研究旨在描述中性粒细胞减少的PID儿童与健康对照组相比龈下牙菌斑微生物组的特征,并评估他们对非手术牙周治疗的反应。方法分别从大奥蒙德街医院(Great Ormond Street Hospital)和巴茨健康NHS信托基金(Barts Health NHS Trust)招募的患有PID的儿童(n = 24)和系统健康对照组(n = 24),在基线和治疗后6个月分别从3颗第一磨牙和1颗第一门牙上收集牙龈下菌斑。采用Illumina元条形码方法对细菌16S rRNA基因V1-V2区域进行龈下微生物组分析。结果通过α和β多样性测量,观察到治疗后社区结构的显著变化。在治疗后的PID患儿中,罗氏菌属、奈瑟菌属和放线菌属的数量有所增加,与临床改善一致。PID患儿的基线血液绝对中性粒细胞计数与criptostatus和Gemella spp呈正相关,与saccharibacterium, Capnocytophaga和Porphyromonas spp呈负相关,突出了关键的宿主-微生物关系。结论:非手术牙周治疗可调节中性粒细胞减少的PID儿童的龈下微生物群,揭示了新的宿主-微生物相互作用对健康口腔微生物群的重要作用。
Non-Surgical Periodontal Therapy Modulates Oral Microbiome in Primary Immunodeficient Children
Background and Aim
Primary Immunodeficiencies (PIDs) arise from rare genetic defects affecting humoral and cellular immunity, which can lead to reduced dental plaque control. This study aimed to characterise the subgingival dental plaque microbiome in neutropenic PID children compared to healthy controls and assess their response to non-surgical periodontal therapy.
Methods
Subgingival plaque was collected from three first molars and one first incisor at baseline and 6 months post therapy from children with PID (n = 24) and systematically healthy control participants (n = 24) who were recruited from Great Ormond Street Hospital and Barts Health NHS Trust, respectively. The subgingival microbiome was profiled using an Illumina metabarcoding approach on the bacterial 16S rRNA gene V1–V2 region.
Results
Significant shifts in community structure were observed post therapy, as measured by alpha and beta diversities. An increase in Rothia spp., Neisseria spp. and Actinomyces spp. was noted in PID children post therapy, consistent with clinical improvements. Baseline blood absolute neutrophil counts in PID children were positively associated with
Streptococcus cristatus
and Gemella spp., and negatively with Saccharibacteria, Capnocytophaga and Porphyromonas spp., highlighting key host–microbial relationships.
Conclusion
Non-surgical periodontal therapy modulated the subgingival microbiota in neutropenic PID children, revealing novel host–microbial interactions important for the oral microbiome in health.
期刊介绍:
Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology.
The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope.
The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.