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Maternal humoral factors modulate offspring gut immune homeostasis to mitigate diabetes development

https://doi.org/10.1101/2024.08.28.604371

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What this work says

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

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The changing epidemiology of type 1 diabetes: why is it going through the roof?

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Association between intestinal permeability and faecal microbiota composition in Italian children with beta cell autoimmunity at risk for type 1 diabetes

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MetOrigin: Discriminating the origins of microbial metabolites for integrative analysis of the gut microbiome and metabolome

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Frontline Science: Abnormalities in the gut mucosa of non-obese diabetic mice precede the onset of type 1 diabetes

inferredcites →https://doi.org/10.1007/s00125-008-1022-zopenalex-snapshot

Maternal type 1 diabetes reduces the risk of islet autoantibodies: relationships with birthweight and maternal HbA1c

inferredcites →https://doi.org/10.1007/s00125-019-4942-xopenalex-snapshot

Early-life factors contributing to type 1 diabetes

inferredcites →https://doi.org/10.1007/s00125-019-4952-8openalex-snapshot

Characteristics of familial type 1 diabetes: effects of the relationship to the affected family member on phenotype and genotype at diagnosis

inferredcites →https://doi.org/10.1007/s00125-020-05287-1openalex-snapshot

Association between family history, early growth and the risk of beta cell autoimmunity in children at risk for type 1 diabetes

inferredcites →https://doi.org/10.1007/s001250051044openalex-snapshot

Familial Risk of Type I diabetes in European Children

inferredcites →https://doi.org/10.1016/j.bbcan.2012.03.008openalex-snapshot

The multifaceted roles of neutrophil gelatinase associated lipocalin (NGAL) in inflammation and cancer

inferredcites →https://doi.org/10.1016/j.cell.2016.04.055openalex-snapshot

Maternal IgG and IgA Antibodies Dampen Mucosal T Helper Cell Responses in Early Life

inferredcites →https://doi.org/10.1016/j.cell.2018.11.035openalex-snapshot

Recirculating Intestinal IgA-Producing Cells Regulate Neuroinflammation via IL-10

inferredcites →https://doi.org/10.1016/j.celrep.2021.109655openalex-snapshot

The gut microbiota induces Peyer’s-patch-dependent secretion of maternal IgA into milk

inferredcites →https://doi.org/10.1016/j.chom.2015.01.001openalex-snapshot

The Dynamics of the Human Infant Gut Microbiome in Development and in Progression toward Type 1 Diabetes

inferredcites →https://doi.org/10.1016/j.chom.2015.07.003openalex-snapshot

Inhibition of Dectin-1 Signaling Ameliorates Colitis by Inducing Lactobacillus-Mediated Regulatory T Cell Expansion in the Intestine

inferredcites →https://doi.org/10.1016/j.chom.2018.12.015openalex-snapshot

Maternal Immunization Confers Protection to the Offspring against an Attaching and Effacing Pathogen through Delivery of IgG in Breast Milk

inferredcites →https://doi.org/10.1016/j.chom.2020.06.009openalex-snapshot

Breastmilk Feeding Practices Are Associated with the Co-Occurrence of Bacteria in Mothers’ Milk and the Infant Gut: the CHILD Cohort Study

inferredcites →https://doi.org/10.1016/j.cmet.2015.03.001openalex-snapshot

Regulation of Obesity-Related Insulin Resistance with Gut Anti-inflammatory Agents

inferredcites →https://doi.org/10.1016/j.ebiom.2023.104567openalex-snapshot

Alterations of the intestinal mucus layer correlate with dysbiosis and immune dysregulation in human Type 1 Diabetes

inferredcites →https://doi.org/10.1016/j.immuni.2019.02.014openalex-snapshot

A Weaning Reaction to Microbiota Is Required for Resistance to Immunopathologies in the Adult

inferredcites →https://doi.org/10.1016/j.pcl.2012.10.002openalex-snapshot

Human Milk Composition

inferredcites →https://doi.org/10.1016/s2213-8587(22)00218-2openalex-snapshot

Global incidence, prevalence, and mortality of type 1 diabetes in 2021 with projection to 2040: a modelling study

inferredcites →https://doi.org/10.1038/mi.2010.23openalex-snapshot

Breast milk immune complexes are potent inducers of oral tolerance in neonates and prevent asthma development

inferredcites →https://doi.org/10.1038/mi.2012.32openalex-snapshot

Temporal and spatial interplay of microbiota and intestinal mucosa drive establishment of immune homeostasis in conventionalized mice

inferredcites →https://doi.org/10.1038/nature07336openalex-snapshot

Innate immunity and intestinal microbiota in the development of Type 1 diabetes

inferredcites →https://doi.org/10.1038/nature12079openalex-snapshot

Thymus-derived regulatory T cells contribute to tolerance to commensal microbiota

inferredcites →https://doi.org/10.1038/nature16962openalex-snapshot

Expanding antigen-specific regulatory networks to treat autoimmunity

inferredcites →https://doi.org/10.1038/ncomms8725openalex-snapshot

Active suppression of intestinal CD4+TCRαβ+ T-lymphocyte maturation during the postnatal period

inferredcites →https://doi.org/10.1038/nm.4142openalex-snapshot

The microbiome in early life: implications for health outcomes

inferredcites →https://doi.org/10.1038/nri.2017.111openalex-snapshot

The hygiene hypothesis in autoimmunity: the role of pathogens and commensals

inferredcites →https://doi.org/10.1038/s41423-023-00989-zopenalex-snapshot

A T follicular helper cell origin for T regulatory type 1 cells

inferredcites →https://doi.org/10.1038/s41467-019-11370-yopenalex-snapshot

Gut-associated IgA+ immune cells regulate obesity-related insulin resistance

inferredcites →https://doi.org/10.1038/s41467-023-43652-xopenalex-snapshot

Mutual modulation of gut microbiota and the immune system in type 1 diabetes models

inferredcites →https://doi.org/10.1038/s41577-023-00985-4openalex-snapshot

The immunology of type 1 diabetes

inferredcites →https://doi.org/10.1038/s41586-018-0617-xopenalex-snapshot

Temporal development of the gut microbiome in early childhood from the TEDDY study

inferredcites →https://doi.org/10.1038/s41586-019-1898-4openalex-snapshot

Microbiota-targeted maternal antibodies protect neonates from enteric infection

inferredcites →https://doi.org/10.1038/s41586-020-2564-6openalex-snapshot

Mucosal or systemic microbiota exposures shape the B cell repertoire

inferredcites →https://doi.org/10.1038/s41586-021-03531-1openalex-snapshot

Thymic development of gut-microbiota-specific T cells

inferredcites →https://doi.org/10.1038/s41590-023-01425-0openalex-snapshot

The endogenous repertoire harbors self-reactive CD4+ T cell clones that adopt a follicular helper T cell-like phenotype at steady state

inferredcites →https://doi.org/10.1055/s-0029-1212120openalex-snapshot

The prevalence of IDDM in the first degree relatives of children newly diagnosed with IDDM in Austria — a population-based study

inferredcites →https://doi.org/10.1056/nejm198407193110304openalex-snapshot

Differences in Risk of Insulin-Dependent Diabetes in Offspring of Diabetic Mothers and Diabetic Fathers

inferredcites →https://doi.org/10.1073/pnas.1508740112openalex-snapshot

Microbiota regulates type 1 diabetes through Toll-like receptors

inferredcites →https://doi.org/10.1073/pnas.1706359114openalex-snapshot

Intestinal virome changes precede autoimmunity in type I diabetes-susceptible children

inferredcites →https://doi.org/10.1073/pnas.1712280114openalex-snapshot

Protective major histocompatibility complex allele prevents type 1 diabetes by shaping the intestinal microbiota early in ontogeny

inferredcites →https://doi.org/10.1084/jem.20120504openalex-snapshot

Familial transmission rather than defective innate immunity shapes the distinct intestinal microbiota of TLR-deficient mice

inferredcites →https://doi.org/10.1084/jem.20171163openalex-snapshot

Maternal IgG immune complexes induce food allergen–specific tolerance in offspring

inferredcites →https://doi.org/10.1084/jem.20180427openalex-snapshot

IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria

inferredcites →https://doi.org/10.1084/jem.20220839openalex-snapshot

Stability and heterogeneity in the antimicrobiota reactivity of human milk-derived immunoglobulin A

inferredcites →https://doi.org/10.1093/nar/gkab382openalex-snapshot

MetaboAnalyst 5.0: narrowing the gap between raw spectra and functional insights

inferredcites →https://doi.org/10.1111/all.14736openalex-snapshot

Breastfeeding promotes early neonatal regulatory T‐cell expansion and immune tolerance of non‐inherited maternal antigens

inferredcites →https://doi.org/10.1111/dme.12163openalex-snapshot

Serological testing for coeliac disease in Type 1 diabetes mellitus: is immunoglobulin A level measurement necessary?

inferredcites →https://doi.org/10.1111/j.1365-2222.2008.03096.xopenalex-snapshot

Maternal tolerance achieved during pregnancy is transferred to the offspring via breast milk and persistently protects the offspring from allergic asthma

inferredcites →https://doi.org/10.1111/j.1469-1809.1969.tb00077.xopenalex-snapshot

Heritabilities of liability to diabetes when sex and age at onset are considered

inferredcites →https://doi.org/10.1111/j.1469-1809.1978.tb00929.xopenalex-snapshot

Diabetes mellitus among first‐ and second‐deǵree relatives of early onset diabetics

inferredcites →https://doi.org/10.1111/j.1651-2227.1982.tb09364.xopenalex-snapshot

THE INCIDENCE OF DIABETES MELLITUS IN SWEDISH CHILDREN 0–14 YEARS OF AGE

inferredcites →https://doi.org/10.1111/joim.12607openalex-snapshot

Intestinal alkaline phosphatase at the crossroad of intestinal health and disease – a putative role in type 1 diabetes

inferredcites →https://doi.org/10.1111/nyas.13360openalex-snapshot

Intestinal epithelial claudins: expression and regulation in homeostasis and inflammation

inferredcites →https://doi.org/10.1126/science.aan6619openalex-snapshot

Natural polyreactive IgA antibodies coat the intestinal microbiota

inferredcites →https://doi.org/10.1126/sciimmunol.aao1314openalex-snapshot

Microbial antigen encounter during a preweaning interval is critical for tolerance to gut bacteria

inferredcites →https://doi.org/10.1126/sciimmunol.abc7191openalex-snapshot

Gut microbiota–specific IgA + B cells traffic to the CNS in active multiple sclerosis

inferredcites →https://doi.org/10.1128/mbio.03335-20openalex-snapshot

An Antibiotic-Impacted Microbiota Compromises the Development of Colonic Regulatory T Cells and Predisposes to Dysregulated Immune Responses

inferredcites →https://doi.org/10.1136/gutjnl-2017-314508openalex-snapshot

Akkermansia muciniphila induces gut microbiota remodelling and controls islet autoimmunity in NOD mice

inferredcites →https://doi.org/10.1136/gutjnl-2020-322873openalex-snapshot

Immunoglobulin A–specific deficiency induces spontaneous inflammation specifically in the ileum

inferredcites →https://doi.org/10.1159/000487102openalex-snapshot

The Neonatal Microbiome and Its Partial Role in Mediating the Association between Birth by Cesarean Section and Adverse Pediatric Outcomes

inferredcites →https://doi.org/10.1172/jci.insight.135718openalex-snapshot

Gut microbial metabolites alter IgA immunity in type 1 diabetes

inferredcites →https://doi.org/10.1177/0890334411424729openalex-snapshot

Sharing of Bacterial Strains Between Breast Milk and Infant Feces

inferredcites →https://doi.org/10.1186/1471-2105-14-128openalex-snapshot

Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool

inferredcites →https://doi.org/10.1186/s12876-016-0498-0openalex-snapshot

The mode of delivery affects the diversity and colonization pattern of the gut microbiota during the first year of infants' life: a systematic review

inferredcites →https://doi.org/10.1186/s13099-019-0332-7openalex-snapshot

Is there any association between gut microbiota and type 1 diabetes? A systematic review

inferredcites →https://doi.org/10.1186/s40168-019-0704-8openalex-snapshot

Macronutrient metabolism by the human gut microbiome: major fermentation by-products and their impact on host health

inferredcites →https://doi.org/10.1210/clinem/dgaa590openalex-snapshot

Altered Systemic and Intestinal IgA Immune Responses in Individuals With Type 1 Diabetes

inferredcites →https://doi.org/10.1371/journal.pone.0025792openalex-snapshot

Gut Microbiome Metagenomics Analysis Suggests a Functional Model for the Development of Autoimmunity for Type 1 Diabetes

inferredcites →https://doi.org/10.1371/journal.pone.0122757openalex-snapshot

Evaluation of Serum & Salivary IgA in Patients with Type 1 Diabetes

inferredcites →https://doi.org/10.1371/journal.pone.0188475openalex-snapshot

Distinct fecal and oral microbiota composition in human type 1 diabetes, an observational study

inferredcites →https://doi.org/10.1371/journal.pone.0277273openalex-snapshot

Selective immunoglobulin A deficiency in children with diabetes mellitus: Data from a medical center in Ukraine

inferredcites →https://doi.org/10.1503/cmaj.121189openalex-snapshot

Gut microbiota of healthy Canadian infants: profiles by mode of delivery and infant diet at 4 months

inferredcites →https://doi.org/10.2119/molmed.2011.00195openalex-snapshot

Selective IgA Deficiency in Autoimmune Diseases

inferredcites →https://doi.org/10.21608/ejhm.2021.209971openalex-snapshot

Prevalence of Selective IgA Deficiency in a Sample of Egyptian Patients with Type1 Diabetes Mellitus

inferredcites →https://doi.org/10.2337/db05-1367openalex-snapshot

2-(8-Hydroxy-6-Methoxy-1-Oxo-1H-2-Benzopyran-3-yl) Propionic Acid, an Inhibitor of Angiogenesis, Ameliorates Renal Alterations in Obese Type 2 Diabetic Mice

inferredcites →https://doi.org/10.2337/db12-0526openalex-snapshot

Fecal Microbiota Composition Differs Between Children With β-Cell Autoimmunity and Those Without

inferredcites →https://doi.org/10.2337/db15-0024openalex-snapshot

Materno-Fetal Transfer of Preproinsulin Through the Neonatal Fc Receptor Prevents Autoimmune Diabetes

inferredcites →https://doi.org/10.2337/db21-0382openalex-snapshot

Gut Microbiota Regulate Pancreatic Growth, Exocrine Function, and Gut Hormones

inferredcites →https://doi.org/10.2337/dc18-0777openalex-snapshot

Intestinal Metaproteomics Reveals Host-Microbiota Interactions in Subjects at Risk for Type 1 Diabetes

inferredcites →https://doi.org/10.2337/diab.31.2.136openalex-snapshot

The Pittsburgh Study of Insulin-Dependent Diabetes Mellitus: Risk for Diabetes Among Relatives of IDDM

inferredcites →https://doi.org/10.3389/fendo.2020.00248openalex-snapshot

Prediction and Prevention of Type 1 Diabetes

inferredcites →https://doi.org/10.3389/fimmu.2020.00810openalex-snapshot

Relevance of the Materno-Fetal Interface for the Induction of Antigen-Specific Immune Tolerance

inferredcites →https://doi.org/10.3389/fimmu.2021.649112openalex-snapshot

Innate Mechanisms in Selective IgA Deficiency

inferredcites →https://doi.org/10.3389/fimmu.2021.737964openalex-snapshot

Environmental Determinants of Type 1 Diabetes: From Association to Proving Causality

inferredcites →https://doi.org/10.3389/fimmu.2023.1096323openalex-snapshot

Virus induced dysbiosis promotes type 1 diabetes onset

inferredcites →https://doi.org/10.3389/fimmu.2023.1146082openalex-snapshot

Maternal provisions in type 1 diabetes: Evidence for both protective & pathogenic potential

inferredcites →https://doi.org/10.3389/fnut.2019.00045openalex-snapshot

What's Normal? Microbiomes in Human Milk and Infant Feces Are Related to Each Other but Vary Geographically: The INSPIRE Study

inferredcites →https://doi.org/10.3390/biom12050619openalex-snapshot

Biology of the Extracellular Proteasome

inferredcites →https://doi.org/10.4049/jimmunol.162.5.2521openalex-snapshot

Targeted Deletion of the IgA Constant Region in Mice Leads to IgA Deficiency with Alterations in Expression of Other Ig Isotypes

inferredcites →https://doi.org/10.4093/dmj.2015.39.2.132openalex-snapshot

Selective Immunoglobulin A Deficiency in Type 1 Diabetes Mellitus: A Prevalence Study in Western Sicily (Italy)

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s12032-025-02972-2openalex-snapshot

Impact of gastrointestinal dysbiosis on tryptophan metabolism and neurological cancer progression

inferred← citeshttps://doi.org/10.1016/j.microb.2025.100352openalex-snapshot

The association between the health of the intestines and the human body with Akkermansia muciniphila

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