Dysbiosis of the Oral Ecosystem in Severe Congenital Neutropenia Patients

被引:11
|
作者
Zaura, Egija [1 ,2 ]
Brandt, Bernd W. [1 ,2 ]
Buijs, Mark J. [1 ,2 ]
Emingil, Gulnur [3 ]
Erguz, Merve [3 ]
Karapinar, Deniz Yilmaz [4 ]
Pekpinarli, Burc [5 ]
Bao, Kai [6 ]
Belibasakis, Georgios N. [6 ]
Bostanci, Nagihan [6 ]
机构
[1] Vrije Univ Amsterdam, Acad Ctr Dent Amsterdam ACTA, Dept Prevent Dent, NL-1600 NP Amsterdam, Netherlands
[2] Univ Amsterdam, NL-1600 NP Amsterdam, Netherlands
[3] Ege Univ, Sch Dent, Dept Periodontol, TR-35100 Izmir, Turkey
[4] Ege Univ, Sch Med, Dept Pediat Hematol, TR-35100 Izmir, Turkey
[5] Ege Univ, Sch Dent, Dept Pediat, TR-35100 Izmir, Turkey
[6] Karolinska Inst, Dept Dent Med, Div Oral Dis, S-14104 Huddinge, Sweden
基金
瑞典研究理事会;
关键词
chemokines; congenital neutropenia; cytokines; gingival crevicular fluid; inflammation; microbiota; saliva; ORIGINAL KOSTMANN FAMILY; PERIODONTAL-DISEASE; MORBUS KOSTMANN; DEFICIENCY; STREM-1;
D O I
10.1002/prca.201900058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Purpose To decipher the underlying immunological mechanisms in predisposition to oral microbial dysbiosis in severe congenital neutropenia (SCN) patients. Experimental Design Ten SCN patients (5-23 years old) and 12 healthy controls (5-22 years old) are periodontally examined and provided saliva, subgingival plaque, and gingival crevicular fluid (GCF) samples. The SCN patients received oral hygiene therapy and are re-evaluated after 6 months. Antimicrobial peptides HPN1-3 and LL-37 are assessed in saliva by ELISA. Concentration of 30 cytokines is measured in saliva and GCF by human 30-plex panel, while bacterial profiles of saliva and subgingival plaque are assessed using 16S rDNA amplicon sequencing. Results There is no significant difference in salivary HPN1-3 and LL-37 concentration between the SCN patients and controls. At baseline, clinical, immunological, and microbiological parameters of the patients are indicative of oral ecological dysbiosis. The SCN patients have significantly higher bleeding on probing (BOP)%, GCF volume, and cytokine levels, high bacterial load with low bacterial diversity in saliva. The associations between the microbiome and immunological parameters in the SCN patients differ from those in the healthy individuals. Conclusions and Clinical Relevance SCN patients have a dysregulated immune response toward commensal oral microbiota, which could be responsible for the observed clinical and microbiological signs of dysbiosis.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)
    Faiyaz-Ul-Haquea, M.
    Al-Jefric, A.
    Abalkhail, H. A.
    Toulimat, M.
    Al-Muallimi, M. A.
    Pulicat, M. S.
    Gaafar, A.
    Alaiya, A. A.
    Al-Dayel, F.
    Peltekova, I.
    Zaidi, S. H. E.
    CLINICAL GENETICS, 2009, 76 (06) : 569 - 572
  • [32] Congenital neutropenia
    Ancliff, PJ
    BLOOD REVIEWS, 2003, 17 (04) : 209 - 216
  • [33] Failure in Implant Rehabilitation in a Patient With Severe Congenital Neutropenia (Kostmann Syndrome)
    Marin-Berna, Marian
    Velazquez-Cayon, Rocio-Trinidad
    Torres-Lagares, Daniel
    Hita-Iglesias, Pilar
    Bouferrache, Kahina
    Madrid, Carlos
    Gutierrez-Perez, Jose-Luis
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2012, 70 (04) : E260 - E263
  • [34] Genetics and Pathophysiology of Severe Congenital Neutropenia Syndromes Unrelated to Neutrophil Elastase
    Boztug, Kaan
    Klein, Christoph
    HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2013, 27 (01) : 43 - +
  • [35] Dysbiosis of oral buccal mucosa microbiota in patients with oral lichen planus
    He, Y.
    Gong, D.
    Shi, C.
    Shao, F.
    Shi, J.
    Fei, J.
    ORAL DISEASES, 2017, 23 (05) : 674 - 682
  • [36] Compound Heterozygous HAX1 Mutations in a Swedish Patient With Severe Congenital Neutropenia and No Neurodevelopmental Abnormalities
    Carlsson, Goran
    Elinder, Goran
    Malmgren, Helena
    Trebinska, Alicja
    Grzybowska, Ewa
    Dahl, Niklas
    Nordenskjold, Magnus
    Fadeel, Bengt
    PEDIATRIC BLOOD & CANCER, 2009, 53 (06) : 1143 - 1146
  • [37] Dysbiosis of oral bacteria in patients with chronic kidney disease
    Yasuno, Tetsuhiko
    Tada, Kazuhiro
    Takahashi, Koji
    Watanabe, Maho
    Ito, Kenji
    Arima, Hisatomi
    Masutani, Kosuke
    RENAL REPLACEMENT THERAPY, 2024, 10 (01)
  • [38] Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry
    Zeidler, Cornelia
    Grote, Ulrike A. H.
    Nickel, Anna
    Brand, Beate
    Carlsson, Goeran
    Cortesao, Emilia
    Dufour, Carlo
    Duhem, Caroline
    Notheis, Gundula
    Papadaki, Helen A.
    Tamary, Hannah
    Tjonnfjord, Geir E.
    Tucci, Fabio
    Van Droogenbroeck, Jan
    Vermylen, Christiane
    Voglova, Jaroslava
    Xicoy, Blanca
    Welte, Karl
    HAEMATOLOGICA, 2014, 99 (08) : 1395 - 1402
  • [39] Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia
    Carlsson, Goran
    Fasth, Anders
    Berglof, Elisabet
    Lagerstedt-Robinson, Kristina
    Nordenskjold, Magnus
    Palmblad, Jan
    Henter, Jan-Inge
    Fadeel, Bengt
    BRITISH JOURNAL OF HAEMATOLOGY, 2012, 158 (03) : 363 - 369
  • [40] Dysbiosis of gut microbiota in patients with severe COVID-19
    Shimizu, Kentaro
    Hirata, Haruhiko
    Tokuhira, Natsuko
    Motooka, Daisuke
    Nakamura, Shota
    Ueda, Akiko
    Tachino, Jotaro
    Koide, Moe
    Uchiyama, Akinori
    Ogura, Hiroshi
    Oda, Jun
    ACUTE MEDICINE & SURGERY, 2024, 11 (01):