TY - JOUR
T1 - Dysregulation of the Intestinal Microbiome in Patients With Haploinsufficiency of A20
AU - Toyofuku, Etsushi
AU - Takeshita, Kozue
AU - Ohnishi, Hidenori
AU - Kiridoshi, Yuko
AU - Masuoka, Hiroaki
AU - Kadowaki, Tomonori
AU - Nishikomori, Ryuta
AU - Nishimura, Kenichi
AU - Kobayashi, Chie
AU - Ebato, Takasuke
AU - Shigemura, Tomonari
AU - Inoue, Yuzaburo
AU - Suda, Wataru
AU - Hattori, Masahira
AU - Morio, Tomohiro
AU - Honda, Kenya
AU - Kanegane, Hirokazu
N1 - Funding Information:
This work was partly supported by MEXT/JSPS KAKENHI (Grant Number: JP17K10099) and Naoki Tsuchida Research Grant to HK.
Publisher Copyright:
Copyright © 2022 Toyofuku, Takeshita, Ohnishi, Kiridoshi, Masuoka, Kadowaki, Nishikomori, Nishimura, Kobayashi, Ebato, Shigemura, Inoue, Suda, Hattori, Morio, Honda and Kanegane.
PY - 2022/1/28
Y1 - 2022/1/28
N2 - Introduction: Haploinsufficiency of A20 (HA20) is a form of inborn errors of immunity (IEI). IEIs are genetically occurring diseases, some of which cause intestinal dysbiosis. Due to the dysregulation of regulatory T cells (Tregs) observed in patients with HA20, gut dysbiosis was associated with Tregs in intestinal lamina propria. Methods: Stool samples were obtained from 16 patients with HA20 and 15 of their family members. Infant samples and/or samples with recent antibiotics use were excluded; hence, 26 samples from 13 patients and 13 family members were analyzed. The 16S sequencing process was conducted to assess the microbial composition of samples. Combined with clinical information, the relationship between the microbiome and the disease activity was statistically analyzed. Results: The composition of gut microbiota in patients with HA20 was disturbed compared with that in healthy family members. Age, disease severity, and use of immunosuppressants corresponded to dysbiosis. However, other explanatory factors, such as abdominal symptoms and probiotic treatment, were not associated. The overall composition at the phylum level was stable, but some genera were significantly increased or decreased. Furthermore, among the seven operational taxonomic units (OTUs) that increased, two OTUs, Streptococcus mutans and Lactobacillus salivarius, considerably increased in patients with autoantibodies than those without autoantibodies. Discussion: Detailed interaction on intestinal epithelium remains unknown; the relationship between the disease and stool composition change helps us understand the mechanism of an immunological reaction to microorganisms.
AB - Introduction: Haploinsufficiency of A20 (HA20) is a form of inborn errors of immunity (IEI). IEIs are genetically occurring diseases, some of which cause intestinal dysbiosis. Due to the dysregulation of regulatory T cells (Tregs) observed in patients with HA20, gut dysbiosis was associated with Tregs in intestinal lamina propria. Methods: Stool samples were obtained from 16 patients with HA20 and 15 of their family members. Infant samples and/or samples with recent antibiotics use were excluded; hence, 26 samples from 13 patients and 13 family members were analyzed. The 16S sequencing process was conducted to assess the microbial composition of samples. Combined with clinical information, the relationship between the microbiome and the disease activity was statistically analyzed. Results: The composition of gut microbiota in patients with HA20 was disturbed compared with that in healthy family members. Age, disease severity, and use of immunosuppressants corresponded to dysbiosis. However, other explanatory factors, such as abdominal symptoms and probiotic treatment, were not associated. The overall composition at the phylum level was stable, but some genera were significantly increased or decreased. Furthermore, among the seven operational taxonomic units (OTUs) that increased, two OTUs, Streptococcus mutans and Lactobacillus salivarius, considerably increased in patients with autoantibodies than those without autoantibodies. Discussion: Detailed interaction on intestinal epithelium remains unknown; the relationship between the disease and stool composition change helps us understand the mechanism of an immunological reaction to microorganisms.
KW - Lactobacillus salivarius
KW - Streptococcus mutans
KW - haploinsufficiency of A20
KW - inborn errors of immunity
KW - intestinal microbiome
KW - regulatory T cells
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UR - http://www.scopus.com/inward/citedby.url?scp=85124591974&partnerID=8YFLogxK
U2 - 10.3389/fcimb.2021.787667
DO - 10.3389/fcimb.2021.787667
M3 - Article
C2 - 35155270
AN - SCOPUS:85124591974
SN - 2235-2988
VL - 11
JO - Frontiers in cellular and infection microbiology
JF - Frontiers in cellular and infection microbiology
M1 - 787667
ER -