Bidirectional crosstalk between dysbiotic gut microbiota and systemic lupus erythematosus: What is new in therapeutic approaches? DOI Creative Commons
Hasnaa Yaigoub, Nada Fath,

Hasna Tirichen

et al.

Clinical Immunology, Journal Year: 2022, Volume and Issue: 244, P. 109109 - 109109

Published: Sept. 8, 2022

Systemic lupus erythematosus is an autoimmune disease characterized by chronic inflammation and multiple organs damage. Its pathogenesis complex involves factors including gut microbiota. Accumulating evidence indicates the interaction of microbial communities with host immune system to maintain a state homeostasis. Imbalances within composition function may contribute development many diseases SLE. In this review, we aim highlight dysregulation commensal bacteria their metabolites in gastrointestinal tract resulting responses decrypt cross-link between altered microbiota SLE condition. We also provide new insights into targeting as promising therapeutic approach treat manage

Language: Английский

The leaky gut and the gut microbiome in sepsis – targets in research and treatment DOI Creative Commons
Wiwat Chancharoenthana, Supitcha Kamolratanakul, Marcus J. Schultz

et al.

Clinical Science, Journal Year: 2023, Volume and Issue: 137(8), P. 645 - 662

Published: April 1, 2023

Abstract Both a leaky gut (a barrier defect of the intestinal surface) and dysbiosis change in microbial population) are intrinsic to sepsis. While sepsis itself can cause dysbiosis, worsen The syndrome refers status with which there is an increased permeability allowing translocation molecules from into blood circulation. It not just symptom gastrointestinal involvement, but also underlying that develops independently, its presence could be recognized by detection, blood, lipopolysaccharides (1→3)-β-D-glucan (major components microbiota). Gut-dysbiosis consequence reduction some bacterial species microbiome, as mucosal immunity defect, caused hypoperfusion, immune cell apoptosis, variety enteric neuro-humoral-immunity responses. A bacteria produce short-chain fatty acids barriers, leading pathogen molecules, circulation where it causes systemic inflammation. Even fungi might human patients sepsis, even though this has been consistently observed murine models probably because longer duration antibiotic use patients. virobiome partly consists bacteriophages detectable contents different between normal hosts. These alterations altogether interesting target for adjuvant therapies, e.g., faecal transplantation or probiotic therapy. Here, current information on along potential biomarkers, new treatment strategies, future research topics mentioned.

Language: Английский

Citations

34

Probiotics as functional foods: How probiotics can alleviate the symptoms of neurological disabilities DOI Creative Commons
Shadi Aghamohammad,

Asal Hafezi,

Mahdi Rohani

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2023, Volume and Issue: 163, P. 114816 - 114816

Published: May 8, 2023

Neurological disorders are diseases of the central nervous system with progressive loss tissue. One most difficult problems associated neurological is that there no clear treatment for these diseases. In this review, physiopathology some neurodegenerative diseases, etiological causes, drugs used and their side effects, finally role probiotics in controlling symptoms presented. Recently, researchers have focused more on microbiome gut-brain axis, which may play a critical maintaining brain health. Probiotics among important bacteria positive effects balance homeostasis via influencing microbiome. Other functions alleviating include anti-inflammatory properties, short-chain fatty acid production, production various neurotransmitters. The control abnormalities seen led to being referred as "psychobiotic. Given axis imbalance gut etiology disorders, could be considered safe agents positively affect complementary options disorders.

Language: Английский

Citations

21

NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota DOI Open Access
Julia Niño-Narvión, Marina Idalia Rojo-López,

Patricia Martinez-Santos

et al.

Nutrients, Journal Year: 2023, Volume and Issue: 15(13), P. 2992 - 2992

Published: June 30, 2023

The oxidized form of nicotinamide adenine dinucleotide (NAD+) is a critical metabolite for living cells. NAD+ may act either as cofactor many cellular reactions well coenzyme different NAD+-consuming enzymes involved in the physiological homeostasis organs and systems. In mammals, synthesized from tryptophan or other vitamin B3 intermediates that precursors. Recent research suggests precursors play crucial role maintaining integrity gut barrier. Indeed, its deficiency has been associated with enhanced inflammation leakage, dysbiosis. Conversely, NAD+-increasing therapies confer protection against intestinal experimental conditions human patients, accumulating evidence indicating such favorable effects could be, at least part, mediated by concomitant changes composition microbiota. However, mechanisms which NAD+-based treatments affect microbiota are still poorly understood. this context, we have focused specifically on impact dysbiosis animal models. We further explored relationship between improved host metabolism immunity vivo. Overall, comprehensive review aims to provide new perspective effect strategies physiology.

Language: Английский

Citations

16

Lupus exacerbation in ovalbumin-induced asthma in Fc gamma receptor IIb deficient mice, partly due to hyperfunction of dendritic cells DOI Open Access

Thansita Bhunyakarnjanarat,

Jiradej Makjaroen, Wilasinee Saisorn

et al.

Asian Pacific Journal of Allergy and Immunology, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Background: Although allergy might be another factor that exacerbates lupus as demonstrated by several epidemiologic studies, the direct correlation between activities and is still in question. Objective:To explore allergic reaction activities. Methods:The asthma model using ovalbumin (OVA) administration wildtype (WT) Fc gamma receptor IIb deficient (FcgRIIb-/-) mice (a lupus-prone model) together with vitro experiments on bone marrow-derived dendritic cells (DCs) were performed.Results: At 2-weeks-post OVA, both WT FcgRIIb-/-mice similar indicated an elevation of IgE IL-4 serum asthma-liked lung histology (lung weight, inflammatory score, bronchial thickness) increased spleen weight.Apoptosis lungs spleens (activated caspase 3 immunohistochemistry) was detected only OVA-administered FcgRIIb-/-mice.Surprisingly, FcgRIIb-/-mice, active nephritis, anti-dsDNA, proteinuria, renal immune complex deposition (immunohistochemistry analysis) implying impact activities.Meanwhile, creatinine gut permeability defect (FitC-dextran assay endotoxemia) not different OVA versus control.In parallel, FcgRIIb-/-DCs more susceptible to activations lipopolysaccharide (LPS) than DCs CD80 major histocompatibility II (MHC II) flow cytometry analysis.Conclusions: OVA-induced exacerbated activity, possibly due hyper-responsiveness over from loss inhibitory FcgRIIb.The proper control beneficial for lupus.

Language: Английский

Citations

5

Metagenomic symphony of the intestinal ecosystem: How the composition affects the mind DOI Creative Commons
Stefanie Malan‐Müller, David Martín‐Hernández, Javier R. Caso

et al.

Brain Behavior and Immunity, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 1, 2024

Language: Английский

Citations

5

Gut microbiota: a newly identified environmental factor in systemic lupus erythematosus DOI Creative Commons

Kaijin Yao,

Yina Xie,

Jiali Wang

et al.

Frontiers in Immunology, Journal Year: 2023, Volume and Issue: 14

Published: July 18, 2023

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that predominantly affects women of childbearing age and characterized by the damage to multiple target organs. The pathogenesis SLE complex, its etiology mainly involves genetic environmental factors. At present, there still lack effective means cure SLE. In recent years, growing evidence has shown gut microbiota, as an factor, triggers autoimmunity through potential mechanisms including translocation molecular mimicry, leads immune dysregulation, contributes development Dietary intervention, drug therapy, probiotics supplement, fecal microbiome transplantation other ways modulate microbiota appear be treatment for this review, dysbiosis in SLE, linking dysregulation associated with are summarized.

Language: Английский

Citations

13

miR‐10b‐5p rescues leaky gut linked with gastrointestinal dysmotility and diabetes DOI Creative Commons
Hannah Zogg, Rajan Singh, Se Eun Ha

et al.

United European Gastroenterology Journal, Journal Year: 2023, Volume and Issue: 11(8), P. 750 - 766

Published: Sept. 18, 2023

Abstract Background/Aim Diabetes has substantive co‐occurrence with disorders of gut‐brain interactions (DGBIs). The pathophysiological and molecular mechanisms linking diabetes DGBIs are unclear. MicroRNAs (miRNAs) key regulators gut dysmotility. We investigated whether impaired barrier function is regulated by a miRNA, miR‐10b‐5p, Methods created new mouse line using the Mb3Cas12a/Mb3Cpf1 endonuclease to delete mir‐10b globally. Loss studies in knockout (KO) mice were conducted characterize diabetes, dysmotility, dysfunction phenotypes these mice. Gain injecting KO miR‐10b‐5p mimic. Further, we performed miRNA‐sequencing analysis from colonic mucosa KO, wild type, mimic injected confirm (1) deficiency mice, (2) restoration after injection. Results Congenital loss led development hyperglycemia, dysfunction. Gut permeability was increased, but expression tight junction protein Zonula occludens‐1 reduced colon Patients or constipation‐ predominant irritable bowel syndrome, known DGBI that linked leaky gut, had significantly expression. Injection rescued alterations phenotypes. Conclusions Our study uncovered potential pathophysiologic mechanism links both dysmotility lacking miR‐10b‐5p. Treatment reversed diabetic, phenotypes, highlighting translational

Language: Английский

Citations

11

Effects of Aneurysmal Subarachnoid Hemorrhage in Patients Without In-Hospital Infection on FABP-I, LBP, and sCD-14 DOI Open Access

Brigitta Orban,

Diána Simon, Szabina Erdő-Bonyár

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(2), P. 485 - 485

Published: Jan. 8, 2025

Aneurysmal subarachnoid hemorrhage (aSAH) is a serious condition complicated by delayed cerebral ischemia (DCI), where inflammation plays key role. Although altered gut permeability noted in other conditions, its significance aSAH remains unclear. Fatty acid-binding protein (FABP-I), lipopolysaccharide-binding (LBP), and soluble CD-14 (sCD-14) are established markers of barrier dysfunction. This study investigates marker changes early late phases. The included 177 patients 100 controls. Serum samples were collected on days 1 (D1) 9 (D9) after ictus. FABP-I, LBP, sCD-14 levels measured via ELISA, clinical data recorded. Outcomes assessed using the 90-day modified Rankin scale (mRS 0-3 = favorable outcome). FABP-I was significantly lower (p < 0.05), while LBP higher 0.001) compared to did not differ between outcome groups, but elevated unfavorable outcomes 0.001). These differed without in-hospital infection, with DCI during later phase 0.05). In differences groups suggest potential endotoxin release from microbial systems, contributing neuroinflammation influencing outcomes.

Language: Английский

Citations

0

Syk inhibitor attenuates lupus in FcγRIIb−/− mice through the Inhibition of DNA extracellular traps from macrophages and neutrophils via p38MAPK-dependent pathway DOI Creative Commons

Kritsanawan Sae‐khow,

Awirut Charoensappakit, Kanyarat Udompornpitak

et al.

Cell Death Discovery, Journal Year: 2025, Volume and Issue: 11(1)

Published: Feb. 17, 2025

Abstract Spleen tyrosine kinase (Syk), an important hub of immune signaling, is activated by several signalings in active lupus which could be interfered Syk inhibitor but still not completely evaluated innate cells associated with activity. Hence, a (fostamatinib; R788) was tested vivo using Fc gamma receptor-deficient (FcγRIIb −/− ) mice and vitro (macrophages neutrophils). After 4 weeks oral inhibitor, 40 week-old FcγRIIb (a full-blown model) demonstrated less prominent parameters (serum anti-dsDNA, proteinuria, glomerulonephritis), systemic inflammation, as serum TNFa, IL-6, citrullinated histone H3 (CitH3), gut permeability defect, indicated FITC dextran assay, lipopolysaccharide (LPS), (1 → 3)-β-D-glucan (BG), extracellular traps (ETs) complex deposition spleens kidneys (immunofluorescent staining CitH3 immunoglobulin G) than placebo. Due to the spontaneous elevation LPS BG serum, plus (LPS + BG) used activate macrophages neutrophils. stimulation, neutrophils predominant abundance phosphorylated (Western blotting), pro-inflammatory responses (CD86 flow cytometry analysis, supernatant cytokines, ETs immunofluorescent, cytometry-based apoptosis). With RNA sequencing analysis western blotting, Syk-p38MAPK-dependent pathway suggested downregulating inflammatory pathways BG-activated Although both inhibitors against p38MAPK attenuated macrophage neutrophil WGP, apoptosis inhibition observed. These results that (fostamatinib) improved severity caused defect partly through Syk-p38MAPK anti-inflammation inhibited ET formation cytokine production from cells.

Language: Английский

Citations

0

The emerging role of neutrophil extracellular traps in autoimmune and autoinflammatory diseases DOI Creative Commons

Liuting Zeng,

Xiang Wang, Wei Xiao

et al.

MedComm, Journal Year: 2025, Volume and Issue: 6(3)

Published: March 1, 2025

Neutrophil extracellular traps (NETs) are unique fibrous structures released by neutrophils in response to various pathogens, exhibiting both anti-inflammatory and proinflammatory effects. In autoimmune conditions, NETs serve as crucial self-antigens triggering inflammatory cascades activating the inflammasome complement systems, disrupting self-tolerance mechanisms accelerating responses. Furthermore, play a pivotal role modulating immune cell activation, affecting adaptive This review outlines intricate relationship between diseases, including arthritis, systemic Behçet's disease, lupus erythematosus, kidney skin sclerosis, vasculitis, gouty arthritis. It highlights potential of targeting therapeutic strategy diseases. By examining dynamic balance NET formation clearance this offers critical insights theoretical foundation for future research on NET-related mechanisms. Advances systems biology, flow cytometry, single-cell multiomics sequencing have provided valuable tools exploring molecular NETs. These advancements renewed focus offering promising avenues further investigation into their clinical implications.

Language: Английский

Citations

0