IntestinalMicrobiota Transplant Prior toAllogeneicStem CellTransplant (MAST) trial: study protocol for a multicentre, double-blinded, placebo-controlled, phase IIa trial DOI Creative Commons
Benjamin H. Mullish, Andrew J. Innes,

Lauren A. Roberts

и другие.

BMJ Open, Год журнала: 2024, Номер 14(12), С. e093120 - e093120

Опубликована: Дек. 1, 2024

Introduction Lower diversity of the gut microbiome prior to allogeneic haematopoietic cell transplantation (HCT) correlates with reduced survival after intervention. Most patients undergoing HCT for a haematological malignancy have previously received intensive chemotherapy, resulting in prolonged neutropenic episodes requiring broad-spectrum antibiotics; use these has been linked diversity. Intestinal microbiota transplant (IMT) is novel treatment approach that restores this We hypothesised IMT performed initiation conditioning during early stages HCT, leading decreased frequency complications and improved outcomes HCT. Methods analysis 50 adult receiving will be recruited into phase IIa trial randomised 1:1 receive capsulised or matched placebo shortly followed up 12 months. The primary outcome assess increase alpha between pre-IMT measured at ~42 days administration (day +28 HCT), comparing difference compared placebo. Secondary include tolerability, dynamics metrics taxonomy over all time points assessed, as well clinical (including burden invasive infections, fever, admission care, development graft-vs-host disease mortality). Ethics dissemination This study was approved by UK Research Committee (REC reference: 23/NE/0105). Dissemination results concert patient public involvement group input expected primarily via abstract presentation conferences manuscripts peer-reviewed journals. Trial registration numbers NCT6355583 ; EudraCT: 2022-003617-10.

Язык: Английский

The Complex Role of Gut Microbiota in Systemic Lupus Erythematosus and Lupus Nephritis: From Pathogenetic Factor to Therapeutic Target DOI Creative Commons
E Parodi,

M. Novi,

Paolo Bottino

и другие.

Microorganisms, Год журнала: 2025, Номер 13(2), С. 445 - 445

Опубликована: Фев. 18, 2025

The role of gut microbiota (GM) and intestinal dysbiosis in triggering the onset and/or modulating severity progression lupus nephritis (LN) has been object intense research over last few years. Some alterations at phyla level, such as abundance Proteobacteria reduction Firmicutes/Bacteroidetes (F/B) ratio α-diversity have consistently reported systemic erythematosus (SLE), whereas a more specific ascribed to some species (Bacteroides thetaiotaomicron Ruminococcus gnavus) LN. Underlying mechanisms include microbial translocation through "leaky gut" subsequent molecular mimicry, immune dysregulation (alteration IFNγ levels balance between Treg Th17 subsets), epigenetic interactions. Levels bacterial metabolites, butyrate other short-chain fatty acids (SCFAs), appear play key Beyond components GM, virome mycobiome are also increasingly recognized important players modulation an response. On hand, microbiota-based therapy appears promising includes diet, prebiotics, probiotics, symbiotics, fecal transplantation (FMT). could correct critical alterations, F/B Treg/Th17 imbalance, blunt production autoantibodies renal damage. Despite current limits, GM is emerging powerful environmental factor that be harnessed interfere with leading SLE, preventing flares organ damage, including aim this review provide state-of-the-art analysis SLE LN on one while exploring possible therapeutic manipulation control disease hand.

Язык: Английский

Процитировано

1

Harnessing the human gut microbiota: an emerging frontier in combatting multidrug-resistant bacteria DOI Creative Commons
Wenwen Ding, Yiwen Cheng, Xia Liu

и другие.

Frontiers in Immunology, Год журнала: 2025, Номер 16

Опубликована: Март 17, 2025

Antimicrobial resistance (AMR) has become a major and escalating global health threat, undermining the effectiveness of current antibiotic antimicrobial therapies. The rise multidrug-resistant bacteria led to increasingly difficult-to-treat infections, resulting in higher morbidity, mortality, healthcare costs. Tackling this crisis requires development novel agents, optimization therapeutic strategies, initiatives infection surveillance control. Recent studies highlight crucial role human gut microbiota defending against AMR pathogens. A balanced protects body through mechanisms such as colonization resistance, positioning it key ally fight AMR. In contrast, dysbiosis disrupts defense, thereby facilitating persistence, colonization, dissemination resistant This review will explore how influence drug-resistant bacterial its involvement various types AMR-related potential for microbiota-targeted therapies, fecal transplantation, prebiotics, probiotics, phage therapy. Elucidating interactions between pathogens provide critical insights developing strategies prevent treat infections. While previous reviews have focused on general impact health, specifically look at latest research evolution spread AMR, highlighting strategies.

Язык: Английский

Процитировано

0

Therapeutic potential of fecal microbiota transplantation in colorectal cancer based on gut microbiota regulation: from pathogenesis to efficacy DOI Creative Commons

Chen Gu,

Gengyu Sha, Baoqing Zeng

и другие.

Therapeutic Advances in Gastroenterology, Год журнала: 2025, Номер 18

Опубликована: Янв. 1, 2025

Colorectal cancer (CRC) remains a leading cause of cancer-related deaths worldwide, with its progression intricately linked to gut microbiota dysbiosis. Disruptions in microbial homeostasis contribute tumor initiation, immune suppression, and inflammation, establishing the as key therapeutic target. Fecal transplantation (FMT) has emerged transformative approach restore balance, enhance responses, reshape microenvironment. This review explores mechanisms underlying FMT’s potential, evaluates advantages over other microbiota-based interventions, addresses challenges such donor selection, safety concerns, treatment standardization. Looking forward, integration FMT into personalized CRC therapies requires robust clinical trials identification predictive biomarkers optimize efficacy safety.

Язык: Английский

Процитировано

0

Fecal microbiota transplantation: application scenarios, efficacy prediction, and factors impacting donor-recipient interplay DOI Creative Commons
Yaxin Liu, Xinru Li, Yuchao Chen

и другие.

Frontiers in Microbiology, Год журнала: 2025, Номер 16

Опубликована: Март 25, 2025

Fecal microbiota transplantation (FMT) represents a therapeutic approach that directly regulates the gut of recipients, normalizes its composition and reaping rewards. Currently, in addition to general application treating Clostridium difficile ( C. ) infection (CDI), FMT treatment has also been extended fields other gastrointestinal diseases, infections, gut-liver or gut-brain axis disorders, metabolic diseases cancer, etc. Prior FMT, rigorous donor screening is essential reduce occurrence adverse events. In addition, it imperative evaluate whether recipient can safely effectively undergo treatment. However, efficacy influenced by complex interactions between recipient, degree engraftment not necessarily positively related with success rate FMT. Furthermore, an increasing number novel factors affecting outcomes are being identified recent clinical trials animal experiments, broadening our understanding This article provides comprehensive review scenarios influencing safety from aspects both donors summarizes how these emerging regulatory be combined predict patients undergoing

Язык: Английский

Процитировано

0

Fecal microbiota transplantation: a tale of two regulatory pathways DOI Creative Commons
Diane E. Hoffmann,

Gail Javitt,

Colleen Kelly

и другие.

Gut Microbes, Год журнала: 2025, Номер 17(1)

Опубликована: Апрель 29, 2025

Fecal microbiota transplantation (FMT) is a procedure involving the transfer of intestinal from healthy donor to patient restore functional microbiome. First described in modern science 1958, use FMT has been practiced for decades, but only during past dozen years have clinical frameworks and legal regulations competent authorities developed. Future development microbiota-derived medical therapies will be shaped by regulatory various jurisdictions. This review examines historical status United States Europe, with particular attention their respective approaches ensuring safety quality therapeutic product access.

Язык: Английский

Процитировано

0

IntestinalMicrobiota Transplant Prior toAllogeneicStem CellTransplant (MAST) trial: study protocol for a multicentre, double-blinded, placebo-controlled, phase IIa trial DOI Creative Commons
Benjamin H. Mullish, Andrew J. Innes,

Lauren A. Roberts

и другие.

BMJ Open, Год журнала: 2024, Номер 14(12), С. e093120 - e093120

Опубликована: Дек. 1, 2024

Introduction Lower diversity of the gut microbiome prior to allogeneic haematopoietic cell transplantation (HCT) correlates with reduced survival after intervention. Most patients undergoing HCT for a haematological malignancy have previously received intensive chemotherapy, resulting in prolonged neutropenic episodes requiring broad-spectrum antibiotics; use these has been linked diversity. Intestinal microbiota transplant (IMT) is novel treatment approach that restores this We hypothesised IMT performed initiation conditioning during early stages HCT, leading decreased frequency complications and improved outcomes HCT. Methods analysis 50 adult receiving will be recruited into phase IIa trial randomised 1:1 receive capsulised or matched placebo shortly followed up 12 months. The primary outcome assess increase alpha between pre-IMT measured at ~42 days administration (day +28 HCT), comparing difference compared placebo. Secondary include tolerability, dynamics metrics taxonomy over all time points assessed, as well clinical (including burden invasive infections, fever, admission care, development graft-vs-host disease mortality). Ethics dissemination This study was approved by UK Research Committee (REC reference: 23/NE/0105). Dissemination results concert patient public involvement group input expected primarily via abstract presentation conferences manuscripts peer-reviewed journals. Trial registration numbers NCT6355583 ; EudraCT: 2022-003617-10.

Язык: Английский

Процитировано

0