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Dysbiosis in the Gut Microbiota of Patients with Multiple Sclerosis, with a Striking Depletion of Species Belonging to Clostridia XIVa and IV Clusters

https://doi.org/10.1371/journal.pone.0137429
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ana.1032openalex-snapshot
Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis
inferredcites →https://doi.org/10.1002/ana.21141openalex-snapshot
Environmental risk factors for multiple sclerosis. Part II: Noninfectious factors
inferredcites →https://doi.org/10.1002/ibd.21436openalex-snapshot
Highlighting new phylogenetic specificities of Crohnʼs disease microbiota
inferredcites →https://doi.org/10.1007/978-1-4614-7953-6openalex-snapshot
Multiple Sclerosis Immunology
inferredcites →https://doi.org/10.1007/978-1-4614-7953-6_6openalex-snapshot
Diet, Gut Flora, and Multiple Sclerosis: Current Research and Future Perspectives
inferredcites →https://doi.org/10.1016/j.cell.2014.03.011openalex-snapshot
Role of the Microbiota in Immunity and Inflammation
inferredcites →https://doi.org/10.1016/j.chom.2008.05.001openalex-snapshot
Metagenomic Approaches for Defining the Pathogenesis of Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.1016/j.jns.2012.08.032openalex-snapshot
Increased prevalence, incidence, and female predominance of multiple sclerosis in northern Japan
inferredcites →https://doi.org/10.1038/cti.2013.11openalex-snapshot
Bacterial lipodipeptide, Lipid 654, is a microbiome‐associated biomarker for multiple sclerosis
inferredcites →https://doi.org/10.1038/ismej.2010.133openalex-snapshot
UniFrac: an effective distance metric for microbial community comparison
inferredcites →https://doi.org/10.1038/nature08821openalex-snapshot
A human gut microbial gene catalogue established by metagenomic sequencing
inferredcites →https://doi.org/10.1038/nature10251openalex-snapshot
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
inferredcites →https://doi.org/10.1038/nature10554openalex-snapshot
Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination
inferredcites →https://doi.org/10.1038/nature11319openalex-snapshot
Gut microbiota composition correlates with diet and health in the elderly
inferredcites →https://doi.org/10.1038/nature12198openalex-snapshot
Gut metagenome in European women with normal, impaired and diabetic glucose control
inferredcites →https://doi.org/10.1038/nature12331openalex-snapshot
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota
inferredcites →https://doi.org/10.1038/nature12506openalex-snapshot
Richness of human gut microbiome correlates with metabolic markers
inferredcites →https://doi.org/10.1038/nature12721openalex-snapshot
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
inferredcites →https://doi.org/10.1038/nature12723openalex-snapshot
The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality
inferredcites →https://doi.org/10.1038/nature12726openalex-snapshot
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
inferredcites →https://doi.org/10.1056/nejmra020100openalex-snapshot
The Effect of Infections on Susceptibility to Autoimmune and Allergic Diseases
inferredcites →https://doi.org/10.1073/pnas.0706625104openalex-snapshot
Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases
inferredcites →https://doi.org/10.1073/pnas.0804812105openalex-snapshot
Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients
inferredcites →https://doi.org/10.1073/pnas.1000082107openalex-snapshot
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1093/dnares/dst006openalex-snapshot
Robustness of Gut Microbiota of Healthy Adults in Response to Probiotic Intervention Revealed by High-Throughput Pyrosequencing
inferredcites →https://doi.org/10.1093/dnares/dst037openalex-snapshot
Dysbiosis of Salivary Microbiota in Inflammatory Bowel Disease and Its Association With Oral Immunological Biomarkers
inferredcites →https://doi.org/10.1099/ijs.0.069146-0openalex-snapshot
The status of the name Lactobacillus rogosae Holdeman and Moore 1974. Opinion 88.Judicial Commission of the International Committee on Systematics of Prokaryotes
inferredcites →https://doi.org/10.1126/science.1198469openalex-snapshot
Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species
inferredcites →https://doi.org/10.1126/science.1241165openalex-snapshot
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
inferredcites →https://doi.org/10.1128/iai.00803-13openalex-snapshot
Serine Lipids of Porphyromonas gingivalis Are Human and Mouse Toll-Like Receptor 2 Ligands
inferredcites →https://doi.org/10.1128/mbio.00261-11openalex-snapshot
Application of Novel PCR-Based Methods for Detection, Quantitation, and Phylogenetic Characterization of Sutterella Species in Intestinal Biopsy Samples from Children with Autism and Gastrointestinal Disturbances
inferredcites →https://doi.org/10.1136/gut.2003.025403openalex-snapshot
Reduction in diversity of the colonic mucosa associated bacterial microflora in patients with active inflammatory bowel disease
inferredcites →https://doi.org/10.1136/gut.2005.073817openalex-snapshot
Reduced diversity of faecal microbiota in Crohn’s disease revealed by a metagenomic approach
inferredcites →https://doi.org/10.1136/gut.2010.223263openalex-snapshot
Dysbiosis of the faecal microbiota in patients with Crohn's disease and their unaffected relatives
inferredcites →https://doi.org/10.1136/gutjnl-2014-308341openalex-snapshot
Geographical patterns of the standing and active human gut microbiome in health and IBD
inferredcites →https://doi.org/10.1177/1352458508098372openalex-snapshot
Temporal changes and geographical differences in multiple sclerosis phenotypes in Japanese: nationwide survey results over 30 years
inferredcites →https://doi.org/10.1371/journal.pone.0027076openalex-snapshot
A Comprehensive Evaluation of Colonic Mucosal Isolates of Sutterella wadsworthensis from Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1371/journal.pone.0063686openalex-snapshot
Characterization of Adherent Bacteroidales from Intestinal Biopsies of Children and Young Adults with Inflammatory Bowel Disease
inferredcites →https://doi.org/10.2353/ajpath.2008.080622openalex-snapshot
NKT Cell-Dependent Amelioration of a Mouse Model of Multiple Sclerosis by Altering Gut Flora
inferredcites →https://doi.org/10.4049/jimmunol.1001443openalex-snapshot
Central Nervous System Demyelinating Disease Protection by the Human Commensal Bacteroides fragilis Depends on Polysaccharide A Expression
inferredcites →https://doi.org/10.7554/elife.01202openalex-snapshot
Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Propionic Acid Shapes the Course of Multiple Sclerosis by a Distinct Immunomodulatory and Neuroprotective Mechanism
inferred← citeshttps://doi.org/10.2139/ssrn.4886559openalex-extracted
inferred← citeshttps://doi.org/10.1002/acn3.465openalex-snapshot
CD 4+ T cells from multiple sclerosis patients respond to a commensal‐derived antigen
inferred← citeshttps://doi.org/10.1002/acn3.51004openalex-snapshot
Gut microbiome variation is associated to Multiple Sclerosis phenotypic subtypes
inferred← citeshttps://doi.org/10.1002/acn3.51476openalex-snapshot
The gut microbiota in pediatric multiple sclerosis and demyelinating syndromes
inferred← citeshttps://doi.org/10.1002/acn3.52259openalex-snapshot
Short‐chain fatty acids in multiple sclerosis: Associated with disability, number of T2 lesions, and inflammatory profile
inferred← citeshttps://doi.org/10.1002/acn3.70212openalex-snapshot
Relapsing–Remitting Multiple Sclerosis Is Associated With a Dysbiotic Oral Microbiome
inferred← citeshttps://doi.org/10.1002/ana.24718openalex-snapshot
Gut microbiome analysis in neuromyelitis optica reveals overabundance of Clostridium perfringens
inferred← citeshttps://doi.org/10.1002/ana.24901openalex-snapshot
The gut microbiome in human neurological disease: A review
inferred← citeshttps://doi.org/10.1002/ana.25244openalex-snapshot
A probiotic modulates the microbiome and immunity in multiple sclerosis
inferred← citeshttps://doi.org/10.1002/ana.26084openalex-snapshot
Gut Microbiome in Progressive Multiple Sclerosis
inferred← citeshttps://doi.org/10.1002/ana.26202openalex-snapshot
Th1 ‐ CD11c + B Cell Axis Associated with Response to Plasmapheresis in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1002/anbr.202500233openalex-snapshot
Decoding the Pathophysiology of Autoimmune Diseases—Mechanism, Triggers, and Nanotherapeutics: A Review
inferred← citeshttps://doi.org/10.1002/cpz1.314openalex-snapshot
Microbiome Methods in Experimental Autoimmune Encephalomyelitis
inferred← citeshttps://doi.org/10.1002/dev.21803openalex-snapshot
A systematic review of gut‐immune‐brain mechanisms in Autism Spectrum Disorder
inferred← citeshttps://doi.org/10.1002/eji.201646792openalex-snapshot
CD44 deletion leading to attenuation of experimental autoimmune encephalomyelitis results from alterations in gut microbiome in mice
inferred← citeshttps://doi.org/10.1002/eji.201847807openalex-snapshot
The role of the gut microbiota and microbial metabolites in neuroinflammation
inferred← citeshttps://doi.org/10.1002/eji.202250229openalex-snapshot
Microbiota, diet, and the gut–brain axis in multiple sclerosis and stroke
inferred← citeshttps://doi.org/10.1002/eji.202250236openalex-snapshot
Diet‐microbiome‐immune interplay in multiple sclerosis: Understanding the impact of phytoestrogen metabolizing gut bacteria
inferred← citeshttps://doi.org/10.1002/ejsc.12166openalex-snapshot
Impact of dance classes on motor and cognitive functions and gut microbiota composition in multiple sclerosis patients: Randomized controlled trial
inferred← citeshttps://doi.org/10.1002/ijc.31836openalex-snapshot
The bidirectional interaction of the gut microbiome and the innate immune system: Implications for chemotherapy‐induced gastrointestinal toxicity
inferred← citeshttps://doi.org/10.1002/mco2.70228openalex-snapshot
Differences of the 6N and 6J Substrains of C57BL/6 Mice in the Development of Experimental Autoimmune Encephalomyelitis
inferred← citeshttps://doi.org/10.1002/mdc3.12840openalex-snapshot
Gut Vibes in Parkinson's Disease: The Microbiota‐Gut‐Brain Axis
inferred← citeshttps://doi.org/10.1002/med.21584openalex-snapshot
Gut microbiome interventions in human health and diseases
inferred← citeshttps://doi.org/10.1002/mnfr.202300043openalex-snapshot
The Gut Microbiome and Autoimmune Hepatitis: Implications for Early Diagnostic Biomarkers and Novel Therapies
inferred← citeshttps://doi.org/10.1002/mnfr.202400251openalex-snapshot
Interplay of Food‐Derived Bioactive Peptides with Gut Microbiota: Implications for Health and Disease Management
inferred← citeshttps://doi.org/10.1007/5584_2016_25openalex-snapshot
Metagenomic Analysis of Cerebrospinal Fluid from Patients with Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/82_2018_117openalex-snapshot
Fungi as Part of the Microbiota and Interactions with Intestinal Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-030-17971-7_54openalex-snapshot
Using Data Science for Medical Decision Making Case: Role of Gut Microbiome in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/978-3-030-24436-1_2openalex-snapshot
Principles of Immunotherapy
inferred← citeshttps://doi.org/10.1007/978-3-030-91051-8_11openalex-snapshot
Neurodegenerative Diseases and the Gut Microbiota
inferred← citeshttps://doi.org/10.1007/978-3-030-91415-8_2openalex-snapshot
Immune-Microbiota Crosstalk Underlying Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-14023-5_13openalex-snapshot
Gut Microbiota Changes and Parkinson’s Disease: What Do We Know, Which Avenues Ahead
inferred← citeshttps://doi.org/10.1007/978-3-031-84065-4_7openalex-snapshot
How the Interplay Between the Commensal Microbiota, Gut Barrier Integrity, and Mucosal Immunity Regulates Extraintestinal Autoimmune Diseases
inferred← citeshttps://doi.org/10.1007/978-3-032-26410-7_18openalex-snapshot
Microbiome and Diseases: Gut–Brain Axis and Neurological Disorders
inferred← citeshttps://doi.org/10.1007/978-3-319-28609-9_10openalex-snapshot
Gut Microbiota: A Possible Role in the Pathogenesis of Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/978-3-319-28609-9_8openalex-snapshot
Nutrition, Macrobiotics, and the Brain’s Neuroinflammatory Response
inferred← citeshttps://doi.org/10.1007/978-4-431-55594-0_1openalex-snapshot
Cellular Immunity and Multiple Sclerosis: Current Understanding
inferred← citeshttps://doi.org/10.1007/978-981-13-1074-4_14openalex-snapshot
Gut Dysbiosis and Its Treatment in Patients with Functional Dyspepsia
inferred← citeshttps://doi.org/10.1007/978-981-15-2385-4_6openalex-snapshot
Gut Microbiota and Neurologic Diseases and Injuries
inferred← citeshttps://doi.org/10.1007/978-981-16-1626-6_7openalex-snapshot
Gut Microbiome Composition as the Key Factor for Immunomodulation in the Host
inferred← citeshttps://doi.org/10.1007/978-981-16-7672-7_7openalex-snapshot
Microbiota-Gut-Brain Axis in Neurological Disorders
inferred← citeshttps://doi.org/10.1007/978-981-19-3949-5_36-1openalex-snapshot
A Comprehensive Review of Medicinal Herbs Improving Gut-Brain Health
inferred← citeshttps://doi.org/10.1007/978-981-19-4530-4_10openalex-snapshot
Potential Role of Probiotics on Gut Microbiota in Neurological Disease
inferred← citeshttps://doi.org/10.1007/978-981-19-4800-8_11openalex-snapshot
Microorganisms in Pathogenesis and Management of Acute Disseminated Encephalomyelitis (ADEM)
inferred← citeshttps://doi.org/10.1007/978-981-19-4800-8_8openalex-snapshot
Microorganisms in Pathogenesis and Management of Multiple Sclerosis (MS)
inferred← citeshttps://doi.org/10.1007/978-981-33-6236-9_1openalex-snapshot
Gut Bacterial Dysbiosis and Its Clinical Implications
inferred← citeshttps://doi.org/10.1007/978-981-95-7494-0_1openalex-snapshot
The Microbiome-Body Connection: Unraveling the Gut-Brain Axis
inferred← citeshttps://doi.org/10.1007/978-981-97-4288-2_11openalex-snapshot
Emerging Relationship Between the Gut Microbiota and Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1007/978-981-97-4673-6_14openalex-snapshot
Ketogenic Diet: Implications on Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/978-981-99-7557-0_36openalex-snapshot
A Comprehensive Review of Medicinal Herbs Improving Gut-Brain Health
inferred← citeshttps://doi.org/10.1007/978-981-99-8803-7_3openalex-snapshot
The Gut Microbiome and the Central Nervous System (CNS)
inferred← citeshttps://doi.org/10.1007/978-981-99-8803-7_9openalex-snapshot
Gut Microbiota and Altered Behaviour: Target on Neuroimmune Interplays
inferred← citeshttps://doi.org/10.1007/s00005-019-00561-6openalex-snapshot
Gut Microbiota in Neurological Disorders
inferred← citeshttps://doi.org/10.1007/s00018-016-2311-1openalex-snapshot
Environmental factors in autoimmune diseases and their role in multiple sclerosis
inferred← citeshttps://doi.org/10.1007/s00109-021-02085-zopenalex-snapshot
Spinal fluid IgG antibodies from patients with demyelinating diseases bind multiple sclerosis-associated bacteria
inferred← citeshttps://doi.org/10.1007/s00115-020-01012-wopenalex-snapshot
Mikrobiota und Multiple Sklerose
inferred← citeshttps://doi.org/10.1007/s00203-021-02276-9openalex-snapshot
Unravelling the potential of gut microbiota in sustaining brain health and their current prospective towards development of neurotherapeutics
inferred← citeshttps://doi.org/10.1007/s00281-019-00733-8openalex-snapshot
The pathogenicity of Th17 cells in autoimmune diseases
inferred← citeshttps://doi.org/10.1007/s00284-022-03150-7openalex-snapshot
Gastrointestinal Tract, Microbiota and Multiple Sclerosis (MS) and the Link Between Gut Microbiota and CNS
inferred← citeshttps://doi.org/10.1007/s00284-026-04992-1openalex-snapshot
Gut Microbiota and Autoimmune Diseases: The Therapeutic Potential of Probiotics
inferred← citeshttps://doi.org/10.1007/s00401-018-1856-5openalex-snapshot
Interplay among gut microbiota, intestinal mucosal barrier and enteric neuro-immune system: a common path to neurodegenerative diseases?
inferred← citeshttps://doi.org/10.1007/s00431-022-04494-9openalex-snapshot
Intestinal microbiota composition of children with infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and multisystem inflammatory syndrome (MIS-C)
inferred← citeshttps://doi.org/10.1007/s10067-018-04419-8openalex-snapshot
Relative abundance of Megamonas hypermegale and Butyrivibrio species decreased in the intestine and its possible association with the T cell aberration by metabolite alteration in patients with Behcet’s disease (210 characters)
inferred← citeshttps://doi.org/10.1007/s10482-026-02304-yopenalex-snapshot
Faecalibacterium prausnitzii and Akkermansia muciniphila: driving the multiple sclerosis-a systematic review
inferred← citeshttps://doi.org/10.1007/s10482-026-02429-0openalex-snapshot
Difficult relationships between humans and bacteria: associations between multiple sclerosis and the human microbiome
inferred← citeshttps://doi.org/10.1007/s10522-024-10136-4openalex-snapshot
Dysbiosis and fecal microbiota transplant: Contemplating progress in health, neurodegeneration and longevity
inferred← citeshttps://doi.org/10.1007/s10522-026-10389-1openalex-snapshot
Age-driven dysbiosis: gut microbiota in the pathogenesis and treatment of aging disorders
inferred← citeshttps://doi.org/10.1007/s10620-018-5072-xopenalex-snapshot
Under-Evaluated or Unassessed Pathogenic Pathways in Autoimmune Hepatitis and Implications for Future Management
inferred← citeshttps://doi.org/10.1007/s10753-020-01339-1openalex-snapshot
Effects of Lactobacillus casei Strain T2 (IBRC-M10783) on the Modulation of Th17/Treg and Evaluation of miR-155, miR-25, and IDO-1 Expression in a Cuprizone-Induced C57BL/6 Mouse Model of Demyelination
inferred← citeshttps://doi.org/10.1007/s10787-022-01011-0openalex-snapshot
Melatonin and multiple sclerosis: antioxidant, anti-inflammatory and immunomodulator mechanism of action
inferred← citeshttps://doi.org/10.1007/s10875-018-0574-zopenalex-snapshot
Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications
inferred← citeshttps://doi.org/10.1007/s11011-016-9917-8openalex-snapshot
Diet, gut microbiota and cognition
inferred← citeshttps://doi.org/10.1007/s11011-021-00807-3openalex-snapshot
Immune-microbiome interplay and its implications in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1007/s11055-017-0484-1openalex-snapshot
Effects of Probiotic Enterococci and Glatiramer Acetate on the Severity of Experimental Allergic Encephalomyelitis in Rats
inferred← citeshttps://doi.org/10.1007/s11259-024-10588-6openalex-snapshot
Microbiota modulation by the inclusion of Tenebrio molitor larvae as alternative to fermented soy protein concentrate in growing pigs diet
inferred← citeshttps://doi.org/10.1007/s11306-025-02315-2openalex-snapshot
Blood metabolomics improves prediction of central nervous system damage in multiple sclerosis
inferred← citeshttps://doi.org/10.1007/s11357-024-01432-5openalex-snapshot
A review on gut microbiota and miRNA crosstalk: implications for Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s11481-021-10023-6openalex-snapshot
Effects of Orally Administered Cannabidiol on Neuroinflammation and Intestinal Inflammation in the Attenuation of Experimental Autoimmune Encephalomyelitis
inferred← citeshttps://doi.org/10.1007/s11481-025-10212-7openalex-snapshot
Lycopene Supplemented Mediterranean Diet Ameliorates Experimental Autoimmune Encephalomyelitis (EAE) in Mice and Changes Intestinal Microbiome
inferred← citeshttps://doi.org/10.1007/s11910-018-0827-5openalex-snapshot
Insights into the Mechanisms That May Clarify Obesity as a Risk Factor for Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s12017-024-08783-4openalex-snapshot
The Role of Gut-derived Short-Chain Fatty Acids in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s12017-025-08879-5openalex-snapshot
Engineering the Microbiome: a Novel Approach to Managing Autoimmune Diseases
inferred← citeshttps://doi.org/10.1007/s12035-016-9975-2openalex-snapshot
Nitrosative Stress, Hypernitrosylation, and Autoimmune Responses to Nitrosylated Proteins: New Pathways in Neuroprogressive Disorders Including Depression and Chronic Fatigue Syndrome
inferred← citeshttps://doi.org/10.1007/s12035-017-0843-5openalex-snapshot
Multiple Immune-Inflammatory and Oxidative and Nitrosative Stress Pathways Explain the Frequent Presence of Depression in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s12035-022-02990-5openalex-snapshot
The Role of a Gut Microbial-Derived Metabolite, Trimethylamine N-Oxide (TMAO), in Neurological Disorders
inferred← citeshttps://doi.org/10.1007/s12035-025-05194-9openalex-snapshot
Decoding the Gut Microbiota in Multiple Sclerosis Using Nanopore Long-Read Sequencing: Insights into Disease Severity and Subtypes
inferred← citeshttps://doi.org/10.1007/s12035-025-05348-9openalex-snapshot
Microbiota-Derived SCFAs in Multiple Sclerosis: From Immune Priming to Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s12223-018-00674-zopenalex-snapshot
Human gut microbes are susceptible to antimicrobial food additives in vitro
inferred← citeshttps://doi.org/10.1007/s12223-026-01574-3openalex-snapshot
The gut microbiota–miRNA axis in multiple sclerosis: Mechanisms and therapeutic potentials
inferred← citeshttps://doi.org/10.1007/s12272-023-01484-9openalex-snapshot
Herbal medicine and gut microbiota: exploring untapped therapeutic potential in neurodegenerative disease management
inferred← citeshttps://doi.org/10.1007/s13205-026-04885-xopenalex-snapshot
From intake to impact: dietary modulation of the gut-brain axis across health and neurological disease
inferred← citeshttps://doi.org/10.1007/s13311-017-0574-3openalex-snapshot
The Gut Microbiota and Pediatric Multiple Sclerosis: Recent Findings
inferred← citeshttps://doi.org/10.1007/s13311-017-0581-4openalex-snapshot
Diet, Gut Microbiota, and Vitamins D + A in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s13311-017-0587-yopenalex-snapshot
The Role of the Gut Microbiome in Multiple Sclerosis Risk and Progression: Towards Characterization of the “MS Microbiome”
inferred← citeshttps://doi.org/10.1007/s13311-017-0588-xopenalex-snapshot
The “Gut Feeling”: Breaking Down the Role of Gut Microbiome in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s13311-017-0594-zopenalex-snapshot
The Gut Microbiome in Neuromyelitis Optica
inferred← citeshttps://doi.org/10.1007/s13311-017-0598-8openalex-snapshot
Microbiota Signaling Pathways that Influence Neurologic Disease
inferred← citeshttps://doi.org/10.1007/s13311-021-01016-7openalex-snapshot
Selected Clostridia Strains from The Human Microbiota and their Metabolite, Butyrate, Improve Experimental Autoimmune Encephalomyelitis
inferred← citeshttps://doi.org/10.1007/s13668-018-0236-zopenalex-snapshot
The Role of Diet in Multiple Sclerosis: Mechanistic Connections and Current Evidence
inferred← citeshttps://doi.org/10.1007/s40263-023-00986-wopenalex-snapshot
The Role of Gut Dysbiosis and Potential Approaches to Target the Gut Microbiota in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s40588-023-00213-6openalex-snapshot
Gut Microbiota and Autoimmune Diseases: Mechanisms, Treatment, Challenges, and Future Recommendations
inferred← citeshttps://doi.org/10.1007/s43440-024-00642-0openalex-snapshot
Multiple sclerosis: a narrative overview of current pharmacotherapies and emerging treatment prospects
inferred← citeshttps://doi.org/10.1007/s44337-024-00135-2openalex-snapshot
The complex relationship between the microbiota-gut-brain axis and neurodegenerative diseases and future perspectives
inferred← citeshttps://doi.org/10.1016/b978-0-12-802304-4.00012-8openalex-snapshot
Correlating the Gut Microbiome to Health and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-803506-1.00027-9openalex-snapshot
Microbiome
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20071-xopenalex-snapshot
Mapping the Environmental Microbiome
inferred← citeshttps://doi.org/10.1016/b978-0-12-810541-2.00004-xopenalex-snapshot
Gut Microbiota in Health and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-811351-6.00026-7openalex-snapshot
References
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inferred← citeshttps://doi.org/10.1016/b978-0-12-815249-2.00033-6openalex-snapshot
The Gut Microbiome in Autoimmune Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-815249-2.00034-8openalex-snapshot
The Gut Microbiome and Metabolome in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-819178-1.00043-5openalex-snapshot
Diet and the microbiome in precision medicine
inferred← citeshttps://doi.org/10.1016/b978-0-12-819265-8.00012-7openalex-snapshot
Microbiome Based Diseases Diagnostics
inferred← citeshttps://doi.org/10.1016/b978-0-12-819265-8.00040-1openalex-snapshot
Gut Microbiota in Brain diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-819265-8.00065-6openalex-snapshot
Microbiota-Gut-Brain Axis
inferred← citeshttps://doi.org/10.1016/b978-0-12-819265-8.00098-xopenalex-snapshot
Microbiota and Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-823848-6.00012-9openalex-snapshot
Microbiome in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-85415-3.00016-7openalex-snapshot
Allergy and autoimmunity: Share of genetics and environment
inferred← citeshttps://doi.org/10.1016/b978-0-323-88534-8.00041-9openalex-snapshot
Microbiome: Impact of sex on function and characteristics of gut microbiome
inferred← citeshttps://doi.org/10.1016/b978-0-323-89834-8.00020-9openalex-snapshot
Linking diet and gut microbiota in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-91387-4.00009-0openalex-snapshot
Gut Microbiota Links With Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-95582-9.00008-5openalex-snapshot
Lipid metabolism in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/b978-0-323-96128-8.00007-9openalex-snapshot
Microflora impacts immune system and its antitumor function
inferred← citeshttps://doi.org/10.1016/b978-0-323-98338-9.00011-6openalex-snapshot
Microbiome manipulation as a target for eye diseases: Lessons from animal models
inferred← citeshttps://doi.org/10.1016/b978-0-443-18578-6.00005-2openalex-snapshot
Microbiome and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-443-18776-6.00003-7openalex-snapshot
Organ-specific autoimmune disorders
inferred← citeshttps://doi.org/10.1016/b978-0-443-19104-6.00001-2openalex-snapshot
Neuroglia and the microbiota-gut-brain axis
inferred← citeshttps://doi.org/10.1016/b978-0-443-21680-0.00007-9openalex-snapshot
Role of microbiota-gut-brain axis in autoimmunity and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-443-23565-8.00020-xopenalex-snapshot
Bacteria, Viruses, and the Microbiome
inferred← citeshttps://doi.org/10.1016/b978-0-443-23565-8.09996-8openalex-snapshot
References
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Fatty acid metabolism in the progression and resolution of CNS disorders
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Combined therapies to treat complex diseases: The role of the gut microbiota in multiple sclerosis
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Autoimmunity and COVID-19 – The microbiotal connection
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The impact of microbiota-derived short-chain fatty acids on macrophage activities in disease: Mechanisms and therapeutic potentials
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Lifestyle alters GUT-bacteria function: Linking immune response and host
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The sex-specific interaction of the microbiome in neurodegenerative diseases
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Role of the intestinal microbiome in autoimmune diseases and its use in treatments
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Human Gut-Derived Commensal Bacteria Suppress CNS Inflammatory and Demyelinating Disease
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Inhibition of Th1 activation and differentiation by dietary guar gum ameliorates experimental autoimmune encephalomyelitis
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The gut microbiota-induced kynurenic acid recruits GPR35-positive macrophages to promote experimental encephalitis
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Tyzzerella nexilis strains enriched in mobile genetic elements are involved in progressive multiple sclerosis
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The gut microbiome and microbial translocation in multiple sclerosis
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Decrease of blood anti-α1,3 Galactose Abs levels in multiple sclerosis (MS) and clinically isolated syndrome (CIS) patients
inferred← citeshttps://doi.org/10.1016/j.clim.2020.108379openalex-snapshot
Role of diet in regulating the gut microbiota and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.clim.2020.108380openalex-snapshot
Gut dysbiosis and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.clim.2024.110258openalex-snapshot
Reconstruction of Sjögren's syndrome-like sialadenitis by a defined disease specific gut-reactive single TCR and an autoantibody
inferred← citeshttps://doi.org/10.1016/j.cll.2018.10.010openalex-snapshot
Immunologic Effects of the Microbiota in Organ Transplantation
inferred← citeshttps://doi.org/10.1016/j.cmet.2018.05.006openalex-snapshot
Intermittent Fasting Confers Protection in CNS Autoimmunity by Altering the Gut Microbiota
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Gut-brain communication in demyelinating disorders
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The Multibiome: The Intestinal Ecosystem's Influence on Immune Homeostasis, Health, and Disease
inferred← citeshttps://doi.org/10.1016/j.ebiom.2021.103557openalex-snapshot
Alterations of the gut mycobiome in patients with MS
inferred← citeshttps://doi.org/10.1016/j.ebiom.2021.103798openalex-snapshot
Alterations of host-gut microbiome interactions in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.ebiom.2022.103870openalex-snapshot
A multiple sclerosis patient-oriented multiomics analysis tells us where to go next: Commentary for: “Alterations of host-gut microbiome interactions in multiple sclerosis”
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105743openalex-snapshot
A probiotic approach identifies a Treg-centred immunoregulation via modulation of gut microbiota metabolites in people with multiple sclerosis and healthy individuals
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105959openalex-snapshot
Alterations of the nasal and oral microbiota in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.envint.2019.105187openalex-snapshot
Urban-associated diseases: Candidate diseases, environmental risk factors, and a path forward
inferred← citeshttps://doi.org/10.1016/j.envres.2023.116114openalex-snapshot
Impact of environmental characteristics on children's gut microbiota – A pilot study in assessing the role of indoor microbiome and metabolites
inferred← citeshttps://doi.org/10.1016/j.foodres.2021.110675openalex-snapshot
Polysaccharides confer benefits in immune regulation and multiple sclerosis by interacting with gut microbiota
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34092openalex-snapshot
RETRACTED: Gut-brain axis: A cutting-edge approach to target neurological disorders and potential synbiotic application
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The Neurodegenerative Elderly Syndrome (NES) hypothesis: Alzheimer and Parkinson are two faces of the same disease
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Structural characterization and anti-rheumatoid arthritis effects of polysaccharides from Anoectochilus xingrenensis
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Lupus: The microbiome angle
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Dysbiosis of the gut bacteriome, phageome, archaeome, and mycobiome in multiple sclerosis: An in-depth review
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Sodium butyrate ameliorates S100/FCA-induced autoimmune hepatitis through regulation of intestinal tight junction and toll-like receptor 4 signaling pathway
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.12.003openalex-snapshot
Microglia, Lifestyle Stress, and Neurodegeneration
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Antibiotics and autoimmune and allergy diseases: Causative factor or treatment?
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Gut microbiome and multiple sclerosis: New insights and perspective
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Effect of diroximel fumarate on gut dysbiosis and autoimmunity in the central nervous system
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Nutritional and ecological perspectives of the interrelationships between diet and the gut microbiome in multiple sclerosis: Insights from marmosets
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Brain Autoimmunity and Intestinal Microbiota: 100 Trillion Game Changers
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A clinical update on the significance of the gut microbiota in systemic autoimmunity
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Connecting the immune system, systemic chronic inflammation and the gut microbiome: The role of sex
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Safety and efficacy of fecal microbiota transplantation for treatment of systemic lupus erythematosus: An EXPLORER trial
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The immunomodulatory roles of the gut microbiome in autoimmune diseases of the central nervous system: Multiple sclerosis as a model
inferred← citeshttps://doi.org/10.1016/j.jaut.2024.103292openalex-snapshot
Perivascular B cells link intestinal angiogenesis to immunity and to the gut-brain axis during neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2017.07.036openalex-snapshot
Complete genome sequence of Ruminococcaceae bacterium CPB6: A newly isolated culture for efficient n -caproic acid production from lactate
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Therapeutic effect of the total saponin from Panax Japonicus on experimental autoimmune encephalomyelitis by attenuating inflammation and regulating gut microbiota in mice
inferred← citeshttps://doi.org/10.1016/j.jff.2022.105200openalex-snapshot
Effect of prebiotic fermentation products from primary human gut microbiota on an in vitro intestinal model
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Prevalence of Small Intestinal Bacterial Overgrowth in Multiple Sclerosis: a Case-Control Study from China
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Gut environmental factors and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2019.01.004openalex-snapshot
Gut microbiota in neurodegenerative disorders
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Deep DNA metagenomic sequencing reveals oral microbiome divergence between monozygotic twins discordant for multiple sclerosis severity
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The second brain: The connection between gut microbiota composition and multiple sclerosis
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The role of multiple sclerosis therapies on the dynamic of human gut microbiota
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Gut dysbiosis influences the pathophysiology of multiple sclerosis: A case-control study from North India
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