Recent Advances in Our Understanding of the Link between the Intestinal Microbiota and Systemic Lupus Erythematosus DOI Open Access
JW Kim, Seung‐Ki Kwok, Jung‐Yoon Choe

et al.

International Journal of Molecular Sciences, Journal Year: 2019, Volume and Issue: 20(19), P. 4871 - 4871

Published: Sept. 30, 2019

Systemic lupus erythematosus (SLE) is an autoimmune disease featuring enhanced expression of type I interferon (IFN) and autoantibody production triggering inflammation of, damage to, multiple organs. Continuing research efforts focus on how gut microbes trigger systemic autoimmunity SLE. The microbial communities mice humans with have been investigated via high-throughput sequencing. Firmicutes-to-Bacteroidetes ratio consistently reduced in SLE patients, regardless ethnicity. relative abundance Lactobacillus differs from the animal model used (MRL/lpr or NZB/W F1 mice). This may indicate that interactions between host, rather than enrichment certain microbes, are especially significant terms development. Enterococcus gallinarum reuteri, both which possible pathobionts, become translocated into tissue if epithelial barrier impaired. then interact host immune systems, activating IFN pathway inducing production. In addition, molecular mimicry critically link microbiome to Gut commensals patients share protein epitopes Ro60 autoantigen. Ruminococcus gnavus strain cross-reacted native DNA, anti-double-stranded DNA antibody response. Expansion R. paralleled increase activity nephritis. Such insights microbiota enhance our understanding pathogenesis will identify biomarkers predicting active disease.

Language: Английский

Autoimmunity and organ damage in systemic lupus erythematosus DOI
George C. Tsokos

Nature Immunology, Journal Year: 2020, Volume and Issue: 21(6), P. 605 - 614

Published: May 4, 2020

Language: Английский

Citations

439

Human Anti-fungal Th17 Immunity and Pathology Rely on Cross-Reactivity against Candida albicans DOI Creative Commons
Petra Bächer,

Thordis Hohnstein,

Eva Beerbaum

et al.

Cell, Journal Year: 2019, Volume and Issue: 176(6), P. 1340 - 1355.e15

Published: Feb. 21, 2019

Language: Английский

Citations

406

Host–microbiota interactions in immune-mediated diseases DOI
William Ruff, Teri M. Greiling, Martin Kriegel

et al.

Nature Reviews Microbiology, Journal Year: 2020, Volume and Issue: 18(9), P. 521 - 538

Published: May 26, 2020

Language: Английский

Citations

372

Low-Avidity CD4+ T Cell Responses to SARS-CoV-2 in Unexposed Individuals and Humans with Severe COVID-19 DOI Creative Commons
Petra Bächer, Elisa Rosati,

Daniela Esser

et al.

Immunity, Journal Year: 2020, Volume and Issue: 53(6), P. 1258 - 1271.e5

Published: Nov. 26, 2020

Language: Английский

Citations

313

Cross-reactivity between tumor MHC class I–restricted antigens and an enterococcal bacteriophage DOI
Aurélie Fluckiger,

Romain Daillère,

Mohamed Sassi

et al.

Science, Journal Year: 2020, Volume and Issue: 369(6506), P. 936 - 942

Published: Aug. 21, 2020

Phages and cancer immunity Gut bacteria are involved in the education of T cell immune responses, intestinal ecosystem influences anticancer immunity. Fluckiger et al. report microbial antigens that might cross-react with associated tumor cells. They found a type called enterococci harbor bacteriophage modulates responses. In mouse models, administration containing boosted responses after treatment chemotherapy or programmed death protein 1 (PD-1) blockade. humans, presence was improved survival PD-1 immunotherapy. A fraction human cells specific for naturally processed melanoma epitopes appeared to be able recognize peptides. This “molecular mimicry” may represent cross-reactivity between tumors antigens. Science , this issue p. 936

Language: Английский

Citations

302

A Diet-Sensitive Commensal Lactobacillus Strain Mediates TLR7-Dependent Systemic Autoimmunity DOI Creative Commons
Daniel F. Zegarra-Ruiz,

Asmaa El Beidaq,

Alonso J. Iñiguez

et al.

Cell Host & Microbe, Journal Year: 2018, Volume and Issue: 25(1), P. 113 - 127.e6

Published: Dec. 20, 2018

Language: Английский

Citations

258

The impact of the gut microbiome on extra-intestinal autoimmune diseases DOI
Eiji Miyauchi, Chikako Shimokawa, Alex Steimle

et al.

Nature reviews. Immunology, Journal Year: 2022, Volume and Issue: 23(1), P. 9 - 23

Published: May 9, 2022

Language: Английский

Citations

232

Toll-like receptor signalling in B cells during systemic lupus erythematosus DOI Open Access
Simon Fillatreau, Benoît Manfroi, Thomas Dörner

et al.

Nature Reviews Rheumatology, Journal Year: 2020, Volume and Issue: 17(2), P. 98 - 108

Published: Dec. 18, 2020

Language: Английский

Citations

228

Gut microbiota dysbiosis and altered tryptophan catabolism contribute to autoimmunity in lupus-susceptible mice DOI
Seung‐Chul Choi, Josephine Brown, Minghao Gong

et al.

Science Translational Medicine, Journal Year: 2020, Volume and Issue: 12(551)

Published: July 8, 2020

Gut microbiota dysbiosis induces lupus-like autoimmunity in mice through altered tryptophan catabolism.

Language: Английский

Citations

192

Shared gut, but distinct oral microbiota composition in primary Sjögren's syndrome and systemic lupus erythematosus DOI Creative Commons
Taco A. van der Meulen, Hermie J. M. Harmsen, Arnau Vich Vila

et al.

Journal of Autoimmunity, Journal Year: 2018, Volume and Issue: 97, P. 77 - 87

Published: Nov. 9, 2018

Alterations in the microbiota composition of gastro-intestinal tract are suspected to be involved etiopathogenesis two closely related systemic inflammatory autoimmune diseases: primary Sjögren's syndrome (pSS) and lupus erythematosus (SLE). Our objective was assess whether alterations gut oral compositions specific for pSS SLE.16S ribosomal RNA gene sequencing performed on fecal samples from 39 patients, 30 SLE patients 965 individuals general population, as well buccal swab washing same patients. Alpha-diversity, beta-diversity relative abundance individual bacteria were used outcome measures. Multivariate analyses test associations between disease phenotype, taking age, sex, body-mass index, proton-pump inhibitor use sequencing-depth into account possible confounding factors.Fecal differed significantly population controls, but not SLE. characterized by lower bacterial richness, Firmicutes/Bacteroidetes ratio higher Bacteroides species compared with controls. Oral which could partially explained dryness patients.pSS share similar composition, distinguishing while shows disease-specific differences

Language: Английский

Citations

181