Imprinting of the immune system by the microbiota early in life

Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549

The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis

Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413

Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour

Cryan, J. F., & Dinan, T. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3346 · Cited by 4,572

Gut Microbiota Metabolism of Dietary Fiber Influences Allergic Airway Disease and Hematopoiesis

Trompette, A., Gollwitzer, E. S., Yadava, K., Sichelstiel, A. K., Sprenger, N., Ngom-Bru, C., Blanchard, C., Junt, T., Nicod, L. P., Harris, N. L., et al. (2014) · Nature Medicine · doi:10.1038/nm.3444 · Cited by 2,862

Trained immunity: A program of innate immune memory in health and– disease

Netea, M. G., Joosten, L. A. B., Latz, E., Mills, K. H. G., Natoli, G., Stunnenberg, H. G., O’Neill, L. A. J., & Xavier, R. J. (2016) · Science · doi:10.1126/science.aaf1098 · Cited by 2,768

The Effect of Infections on Susceptibility to Autoimmune and Allergic Diseases

Bach, J. (2002) · New England Journal of Medicine · doi:10.1056/nejmra020100 · Cited by 2,723

The Placenta Harbors a Unique Microbiome

Aagaard, K., Ma, J., Antony, K. M., Ganu, R., Petrosino, J., & Versalovic, J. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008599 · Cited by 2,494

How colonization by microbiota in early life shapes the immune system

Gensollen, T., Iyer, S. S., Kasper, D. L., & Blumberg, R. S. (2016) · Science · doi:10.1126/science.aad9378 · Cited by 2,044

Reciprocal T H 17 and Regulatory T Cell Differentiation Mediated by Retinoic Acid

Mucida, D., Park, Y., Kim, G., Turovskaya, O., Scott, I., Kronenberg, M., & Cheroutre, H. (2007) · Science · doi:10.1126/science.1145697 · Cited by 1,982

Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function

Olszak, T., An, D., Zeissig, S., Vera, M. P., Richter, J., Franke, A., Glickman, J. N., Siebert, R., Baron, R. M., Kasper, D. L., et al. (2012) · Science · doi:10.1126/science.1219328 · Cited by 1,661

Diurnal rhythmicity of fecal microbiota and metabolite profiles in the first year of life: a randomized controlled interventional trial with infant formulaPreprint

Heppner, N., Reitmeier, S., Heddes, M., Merino, M. V., Schwartz, L., Dietrich, A., List, M., Gigl, M., Meng, C., Omer, H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.19.563092 · Cited by 2

Competitive Coherence Generates Qualia in Bacteria and Other Living Systems

Norris, V. (2021) · Biology · doi:10.3390/biology10101034 · Cited by 4

Dietary supplementation with Rehmannia glutinosa catalpol improves broiler performance by regulating intestinal immune microenvironment

Mu, Z., Guo, L., Zhou, Y., Nie, F., Li, Z., Liu, H., Cui, J., Huang, M., & Yang, Y. (2024) · Italian Journal of Animal Science · doi:10.1080/1828051x.2024.2406517 · Cited by 1

Breast milk stabilizes bacterial communities in the large intestine even after weaning

Ito, K., Islam, J., Sakurai, K., Koyama, S., Matsuo, A., Okano, K., Hirakawa, R., Furukawa, M., & Nochi, T. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.151585 · Cited by 1

Impact of Micro-nanoplastics on Gut and Immune Function

Singh, C., Singh, R., Shekhar, A., & Das, I. (2025) · Sustainable development goals series · doi:10.1007/978-981-96-5047-7_19 · Cited by 1

Microbial influx during early postnatal life fortifies the ocular surface and guards against allergic eye disease in mice

Liu, Y., Sun, H., Song, S., He, X., Wu, H., Ou, S., He, H., Zong, R., Chen, Y., Fu, G., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-09095-4 · Cited by 1

Microbial interventions to improve health in neonatal ruminants: discoveries to applications

Malmuthuge, N., & Guan, L. L. (2025) · Canadian Journal of Animal Science · doi:10.1139/cjas-2025-0011 · Cited by 1

Early-life B cell memory is archived in the mouse B-1 cell compartment and drives chronic lymphocytic leukemia-like disease

Krausse, N., Vergani, S., Escrivà-Font, J., Montano, G., Boldrin, E., Sodini, S., Muleta, K. G., Soneji, S., Scharer, C. D., Consiglio, C. R., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117202 · Cited by 1

Fecal amino acid and short-chain fatty acid profiles in children with migraine: a targeted metabolomics study

Tian, N., Yang, F., Zhao, Y., Jin, M. H., Sun, F., Liu, M., Lian, Y., Sun, S., & Liu, K. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1788386 · Cited by 1

Trained immunity agonists given to neonatal mice fail to protect against leptospiral infection in adulthood and may cause adverse effects

Fernandez, M., Vernel-Pauillac, F., Pézier, T., Lacroix‐Lamandé, S., & Werts, C. (2026) · Innate Immunity · doi:10.1177/17534259261455983 · Cited by 1

The microbiome protects against septic hyperinflammation and bacterial proliferation in a zebrafish model of blood infection with Escherichia coli and mycobacteria

Liu, L., Koch, B. E. V., Krekels, E. H. J., & Spaink, H. P. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1837804 · Cited by 1

Antibiotic Class-Specific Effects on Inflammatory Bowel Disease: Microbiome Disruption, Risk, and Recovery

Rajarathinam, B., Nair, P. M., Murali, N., Lekshmi, G., Sajeev, A. K., Pillai, A. B., Thomas, A., Hely, S., Arun, K., Prakash, V., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146502 · Cited by 1

Gut-brain-immune interactions in neonatal hypoxic–ischemic brain injury

Herz, J., Bendix, I., Orywal, F., Härtel, C., & Felderhoff‐Müser, U. (2026) · Molecular and Cellular Pediatrics · doi:10.1186/s40348-026-00252-1 · Cited by 1

Early-life immune imprinting by a B. infantis-HMO synbiotic shapes infant immune signatures and protects against experimental respiratory disease

Rashid, R. B., Chung, C. K., Namubiru, P., Ahmed, T., Howard, D. R., Sebina, I., Wilkins, T., Rana, M. S., Morrow, J. P., Creek, D. J., et al. (2026) · Cell Reports Medicine · doi:10.1016/j.xcrm.2026.102935 · Cited by 1

Care of the Newborn Infant during the Third Stage of Labor

Díaz-Rossello, J. L., & Blasina, F. (2021) · Springer eBooks · doi:10.1007/978-3-030-83434-0_53 · Cited by 1

The gut microbiome and severity of SARS-CoV-2 infection: what is the link?

Robalino, J. G., Salazar, P., Muñóz, N., Tene, D. M., & Pedreáñez, A. B. (2022) · Novel Research in Microbiology Journal · doi:10.21608/nrmj.2022.253262 · Cited by 1

Progress on probiotics as add-on therapy for allergic rhinitis

Ciprandi, G., del Giudice, M. M., & Drago, L. (2024) · Revue française d'allergologie · doi:10.1016/j.reval.2023.103766 · Cited by 1

Effects of parental care on skin microbial community composition in poison frogs

Fischer, M., Xue, K. S., Costello, E. K., Dvorak, M., Raboisson, G., Robaczewska, A., Caty, S. N., Relman, D. A., & O’Connell, L. A. (2025) · eLife · doi:10.7554/elife.103331.3 · Cited by 1

Humans and the Microbiome: We Are Many

Lucius, R. (2025) · Springer eBooks · doi:10.1007/978-3-031-78821-5_4 · Cited by 1

Gut microbiota in the etiopathogenesis of celiac disease

Olivares, M., & Sanz, Y. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821594-4.00011-6 · Cited by 1

Editorial: Sustained Effects of Early Nutrition on Immune Development and Microbiome-Immune Crosstalk

Lewis, M. C., Childs, C. E., & Pérez-Cano, F. J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01687 · Cited by 1

Multigenerational adversity impacts on gut microbiome composition and socioemotional functioning in early childhoodPreprint

Querdasi, F. R., Karnani, N., broekman, B., Chong, Y. S., Gluckman, P. D., Daniel, L. M., Yap, F. K. P., Eriksson, J. G., Cai, S., Meaney, M. J., et al. (2022) · doi:10.31234/osf.io/64m9g · Cited by 1

Food allergy prevention in progeny by prebiotics supplementation during pregnancy in a preclinical studyPreprint

Selle, A., Brosseau, C., Duval, A., Bouchaud, G., Rousseaux, A., Bruneau, A., Cherbuy, C., Mariadassou, M., Cariou, V., Barbarot, S., et al. (2024) · doi:10.22541/au.170665900.07520581/v1 · Cited by 1

Fusobacterium necrophorum and Fusobacterium varium are commensal members of the bovine reproductive microbiota and may colonize calf prenatallyPreprint

Kilama, J., Dahlen, C. R., Abbasi, M., Shi, X., Nagaraja, T. G., Crouse, M. S., Cushman, R. A., Snider, A. P., McCarthy, K. L., Caton, J. S. S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.15.618546 · Cited by 1

Effects of parental care on skin microbial community composition in poison frogsPreprint

Fischer, M., Xue, K. S., Costello, E. K., Dvorak, M., Raboisson, G., Robaczewska, A., Caty, S. N., Relman, D. A., & O’Connell, L. A. (2025) · eLife · doi:10.7554/elife.103331 · Cited by 1

Effects of parental care on skin microbial community composition in poison frogsPreprint

Fischer, M., Xue, K. S., Costello, E. K., Dvorak, M., Raboisson, G., Robaczewska, A., Caty, S. N., Relman, D. A., & O’Connell, L. A. (2025) · eLife · doi:10.7554/elife.103331.2 · Cited by 1

Stochastic Variational Variable Selection for High-Dimensional Microbiome DataPreprint

Dang, T., Kumaishi, K., Usui, E., Kobori, S., Sato, T., Toda, Y., Yamasaki, Y., Tsujimoto, H., Ichihashi, Y., & Iwata, H. (2021) · Research Square · doi:10.21203/rs.3.rs-955229/v1

Fetal Exposure to Acetochlor Impaired Cognitive Function in Rats via Abnormal Gut Microbiome and Metabolic DisordersPreprint

Wei, W., Wu, H., Gu, W., Xu, J., Hu, C., Ma, Y., Qi, G., Jiang, H., Long, Y., Jiang, X., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-1057583/v1

Timing matters: Age-dependent impacts of the social environment and host selection on the avian gut microbiotaPreprint

Maracı, Ö., Antonatou-Papaioannou, A., Jünemann, S., Engel, K., Castillo-Gutiérrez, O., Busche, T., Kalinowski, J., & Caspers, B. A. (2022) · Research Square · doi:10.21203/rs.3.rs-1712585/v1

Vous avez dit « immunité » ?

Daëron, M. (2023) · Revue française d'allergologie · doi:10.1016/j.reval.2023.103282

Mechanisms of oral tolerance

Cheifetz, T. R., Muske, J., & Knoop, K. A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-96018-2.00062-6

From Leaky Gut to Tissue Microbiota in Metabolic Diseases

Burcelin, R. (2023) · Endocrinology · doi:10.1007/978-3-031-08115-6_4-1

INFARTO DE ARTÉRIA DE PERCHERON: RELATO DE CASO

Bucater, R. N., Castro, J. E. N. D. M. E., & Beltrame, D. P. C. (2023) · doi:10.22533/at.ed.2522402013

ANÁLISE ABRANGENTE DOS ENIGMAS DA NEUROLOGIA: UMA REVISÃO INTEGRATIVA

de Freitas, D. S., Filho, V. Z., Guerreiro, L. J. R., Moreira, G. D. P., Ramenzoni, F. B. B., Kachani, J., DINIZ, P. D., de Medeiros, D. A. P., Jorge, L. B., Ferreira, Y. D. M., et al. (2023) · doi:10.22533/at.ed.2522402012

PERFIL DAS INTOXICAÇÕES MEDICAMENTOSAS NA REGIÃO NORDESTE ENTRE OS ANOS DE 2014 A 2017

Caiana, R. R. A., Filho, F. C. D. M., Alves, Y. D. S., Ramos, J. F., Silva, R. D. O., & Freitas, J. C. R. (2023) · doi:10.22533/at.ed.2522402015

SECUELAS CARDIOVASCULARES POST-COVID-19 SEGÚN LA EXPERIENCIA DE MÉDICOS TRATANTES

Tapia, I. M. G., Cruz, Y. D., Zermeño, M. D. C. L., Esparza, L. C. H., Garnica, A. R., & Ledezma, J. C. R. (2023) · doi:10.22533/at.ed.2522402017

PERCEPCIÓN DE LA POBLACIÓN SOBRE LA VACUNA CONTRA COVID 19

Saldierna, M. G., Arellano, M. A. R., Chavarria, M. A. Y., Briseño, A. R. A., Martínez, D. V. S., Mendez, F. G., Vázquez, J. R., Zermeño, M. D. C. L., Esparza, L. C. H., Mancera, L. D. T., et al. (2023) · doi:10.22533/at.ed.2522402014

PRÁTICAS DE CUIDADO DOS REMANESCENTES DE QUILOMBO DO MUNICÍPIO DE ORIXIMINÁ, BAIXO AMAZONAS

Soares, M. P., Cheble, A. B. C. D. S., Ramirez, B. G., Calzavara, J. S. I. D. R., Campos, J. C., Galvão, L. S. B., Guimarães, L. M. S., Pinto, L. R. O., Bittencourt, M. A. D. S., & de Rezende, P. P. C. (2023) · doi:10.22533/at.ed.2522402016

Jornada médica: desafios e triunfos na prática da medicina 2

Neto, B. R. D. S. (2023) · doi:10.22533/at.ed.252240201

SEPSE: DESAFIOS DIAGNÓSTICOS E ESTRATÉGIAS DE INTERVENÇÃO

Oyczenascz, B. L. S., de Oliveira, V. A., & Frizzo, M. N. (2023) · doi:10.22533/at.ed.2522402018

TRATAMENTO E PREVENÇÃO IDEAL PARA CICATRIZES DE CIRURGIAS PLÁSTICAS

Torres, C. D. M., Ramos, L. N. R., Torres, K. D. M., Matozinho, D. V. P., de Sá, P. A. T., Perini, R. L. M., de Pina, T. P., Melo, L. R., Filho, A. S., Filho, H. R. D. O., et al. (2023) · doi:10.22533/at.ed.2522402019

AGREGAÇÃO DE EXCESSO DE PESO CORPORAL E PRÁTICA INSUFICIENTE DE ATIVIDADE FÍSICA AUMENTAM PERDA DE PRODUTIVIDADE LABORAL ENTRE OS PACIENTES DO SISTEMA ÚNICO DE SAÚDE

Araújo, M. Y. C., Mantovani, A. M., dos Santos, L. L., Rodrigues, G. D. L., & Codogno, J. S. (2023) · doi:10.22533/at.ed.2522402011

RELAÇÃO ENTRE O MICROBIOMA INTESTINAL E O SISTEMA ABO: UMA REVISÃO BIBLIOGRÁFICA

Nascimento, I. M., & Neto, B. R. D. S. (2023) · doi:10.22533/at.ed.25224020110

From Leaky Gut to Tissue Microbiota in Metabolic Diseases

Burcelin, R. (2024) · Endocrinology · doi:10.1007/978-3-031-35064-1_4

Variability of the intestinal microbiota in children with of noninfectious diseases

Тurdieva, S. T., Ganiyeva, D. K., & Abdurashidova, K. B. (2024) · Meditsinskiy sovet = Medical Council · doi:10.21518/ms2024-203

Microbiota-Based Therapeutics for COVID-19 and Sequelae

de Oliveira, G. L. V. (2024) · Springer eBooks · doi:10.1007/978-981-97-3790-1_22

Effects of parental care on skin microbial community composition in poison frogsPreprint

Fischer, M., Xue, K. S., Costello, E. K., Dvorak, M., Raboisson, G., Robaczewska, A., Caty, S. N., Relman, D. A., & O’Connell, L. A. (2025) · eLife · doi:10.7554/elife.103331.1

Translating Patent Innovation into Clinical Practice: Two Decades of Therapeutic Advancements in Dysbiosis Management

D’Urso, F., Paladini, F., Miraglia, A., D’Amuri, A., Chieppa, M., Pollini, M., & Broccolo, F. (2025) · Microorganisms · doi:10.3390/microorganisms13051064

Intestinal Mucosal Immunity and IgA Shape the Gut Microbiota Composition in Early and Adult Life

Nabhani, Z. A., & Ronchi, F. (2025) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-031-84065-4_5

Early development and dynamics of nasopharyngeal microbiota in infants during the COVID-19 pandemic: a 2-year prospective birth cohort study

Lluansí, A., Brotons, P., Díaz, M., Cases, A. R., García-Beltrán, C., Pérez-Argüello, A., Cisneros, M., Blanco-Fuertes, M., Henares, D., Ibáñez, L., et al. (2025) · Respiratory Research · doi:10.1186/s12931-025-03307-5

Born to be wild: Wildings stay the course

Thomson, C. A., & McCoy, K. D. (2025) · Immunity · doi:10.1016/j.immuni.2025.08.013

Phylosymbiosis in the making: Discordant developmental emergence of evolutionary signatures in the mammalian gut microbiome and host transcriptomePreprint

Rudzki, E. N., Jašarević, E., & Kohl, K. D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.13.682227

Pourquoi les maladies inflammatoires chroniques de l’intestin sont-elles devenues plus fréquentes chez l’enfant ?

Enaud, R., Rivière, P., Poullenot, F., & Lamireau, T. (2025) · Perfectionnement en Pédiatrie · doi:10.1016/j.perped.2025.10.005

Early growth restriction disrupts mice intestinal clock and homeostasis without being prevented by lactoferrin

Tran, L. C., Marousez, L., Micours, E., Dubernat, L., Meneboo, J., Figeac, M., Ribière, C., Bonhomme, C., Gottrand, F., Lésage, J., et al. (2025) · Pediatric Research · doi:10.1038/s41390-025-04466-3

Effect of perinatal ampicillin or amoxicillin/clavulanate exposure on maternal and infant gut microbiome, metabolome, and infant responses to the 20-valent pneumococcal conjugate vaccine

Suzuki, E., Deleray, V., Zemlin, J., Kousha, A., Nonoguchi, H. A., Sun, D., Tsai, C., Zuffa, S., Kvitne, K. E., Dorrestein, P. C., et al. (2026) · Gut Microbes Reports · doi:10.1080/29933935.2026.2705707

The infant gut microbiome and the intergenerational transmission of psychiatric risk

Jopling, E. N., Metcalfe‐Roach, A., Turvey, S. E., Mandhane, P. J., Finlay, B. B., & LeMoult, J. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106232

Additional file 1 of Stochastic variational variable selection for high-dimensional microbiome data

Dang, T., Kumaishi, K., Usui, E., Kobori, S., Sato, T., Toda, Y., Yamasaki, Y., Tsujimoto, H., Ichihashi, Y., & Iwata, H. (2023) · Figshare · doi:10.6084/m9.figshare.22603660

Additional file 3 of Hen raising helps chicks establish gut microbiota in their early life and improve microbiota stability after H9N2 challenge

Li, X., Bi, R., Xiao, K., Roy, A., Zhang, Z., Chen, X., Peng, J., Wang, R., Yang, R., Shen, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19028964

Additional file 2 of Stochastic variational variable selection for high-dimensional microbiome data

Dang, T., Kumaishi, K., Usui, E., Kobori, S., Sato, T., Toda, Y., Yamasaki, Y., Tsujimoto, H., Ichihashi, Y., & Iwata, H. (2023) · Figshare · doi:10.6084/m9.figshare.22603663

Additional file 1 of Hen raising helps chicks establish gut microbiota in their early life and improve microbiota stability after H9N2 challenge

Li, X., Bi, R., Xiao, K., Roy, A., Zhang, Z., Chen, X., Peng, J., Wang, R., Yang, R., Shen, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19028955

Additional file 1 of Agaricus subrufescens fermented rye affects the development of intestinal microbiota, local intestinal and innate immunity in suckling-to-nursery pigs

Wen, C., Geervliet, M., de Vries, H., Fabà, L., den Hil, P. J. R.-V., Skovgaard, K., Savelkoul, H. F. J., Schols, H. A., Wells, J. M., Tijhaar, E. J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26581682

Additional file 1 of Impacts of maternal microbiota and microbial metabolites on fetal intestine, brain, and placenta

Husso, A., Pessa‐Morikawa, T., Koistinen, V., Kärkkäinen, O., Kwon, H. N., Lahti, L., Iivanainen, A., Hanhineva, K., & Niku, M. (2024) · Figshare · doi:10.6084/m9.figshare.26623024

Additional file 4 of Hen raising helps chicks establish gut microbiota in their early life and improve microbiota stability after H9N2 challenge

Li, X., Bi, R., Xiao, K., Roy, A., Zhang, Z., Chen, X., Peng, J., Wang, R., Yang, R., Shen, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19028967

Additional file 5 of Hen raising helps chicks establish gut microbiota in their early life and improve microbiota stability after H9N2 challenge

Li, X., Bi, R., Xiao, K., Roy, A., Zhang, Z., Chen, X., Peng, J., Wang, R., Yang, R., Shen, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19028970

Additional file 2 of Impacts of maternal microbiota and microbial metabolites on fetal intestine, brain, and placenta

Husso, A., Pessa‐Morikawa, T., Koistinen, V., Kärkkäinen, O., Kwon, H. N., Lahti, L., Iivanainen, A., Hanhineva, K., & Niku, M. (2024) · Figshare · doi:10.6084/m9.figshare.26623027

Additional file 2 of Hen raising helps chicks establish gut microbiota in their early life and improve microbiota stability after H9N2 challenge

Li, X., Bi, R., Xiao, K., Roy, A., Zhang, Z., Chen, X., Peng, J., Wang, R., Yang, R., Shen, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19028958

Le triptyque microbiote–immunité–cerveau dans l’inflammation et la cognition

Eberl, G. (2026) · Bulletin de l Académie Nationale de Médecine · doi:10.1016/j.banm.2026.01.008

Accelerating Cancer Risk Factor Discovery for Prevention in Younger GenerationsPreprint

Sarsenova, A. (2026) · doi:10.24108/preprints-3114438

Microbiota humana: Nuestra compañera desde el nacimiento hasta la muerte

García-Martínez, B. I. (2026) · Casos y Revisiones de Salud · doi:10.22201/fesz.26831422e.2025.7.2s.6

Maternal gut microbial legacy shapes intestinal health and susceptibility of offspring to colitis

Lee, J.-M., Kim, M.-J., Hoyul, L., Hyun, Y., Nam, S., Jeon, D.-G., Shin, J., & Kim, E. S. (2026) · npj Biofilms and Microbiomes · doi:10.1038/s41522-026-00938-4 · Cited by 1

Histomorphological analysis of the relationship between Helicobacter pylori infection of the gastric mucosa and host immunity strength

Wang, Y.-K., Guo, Q.-W., He, H.-Y., Li, Y.-Y., Zhu, C.-Y., Li, P., Jiang, B., Wang, S.-N., & Xu, S.-L. (2026) · Journal of Molecular Histology · doi:10.1007/s10735-026-10773-8

Differentiation and activation of Peyer’s patch phagocytes in adulthood and upon weaning

Wagner, C. (2020) · theses.fr (ABES) · doi:10.70675/c0f7e7aazfdf6z474dz826bz26f9444d5035

Etude du rôle de la signalisation du TGF-beta au sein des lymphocytes T dans la tolérance au microbiote intestinal

Benech, N. (2021) · theses.fr (ABES) · doi:10.70675/1b31a851z0f22z458ez95d5z183bb456b0ea

Identification et caractérisation de métabolites lipidiques bactériens impliqués dans l'homéostasie intestinale

Petitfils, C. (2021) · theses.fr (ABES) · doi:10.70675/bc778947z305ez4f0cz8866z05cc7ee3d466

Phagocyte activation processes in Peyer’s patches and development of a strategy to analyse the gut microbiota

Arroyo-Portilla, C. (2021) · theses.fr (ABES) · doi:10.70675/d2f458bfz528bz4f0aza382z0e40544f7556

Role of gut antimicrobial peptides in autoimmune diabetes

Liang, W. (2022) · theses.fr (ABES) · doi:10.70675/c6de56d0z81a5z4ca8zb878z9a08dd3b00c4

Etude de l’effet préventif d’une supplémentation en prébiotiques pendant la grossesse sur la survenue de l’allergie alimentaire chez la descendance

Selle, A. (2021) · theses.fr (ABES) · doi:10.70675/4c12f064zf4b7z40cezb550z1d17af21b730

Barrière intestinale, translocation de composés bactériens et développement de l'arthrite inflammatoire : étude du lien mécanistique

Poline, J. (2022) · theses.fr (ABES) · doi:10.70675/3bf35673z4a77z4947zb0a0z527a68ad6881

Archaea méthanogène et signature immunologique intestinale : caractérisation et relation avec l'évolution allergique à l'âge de 3 ans

Sérémé, Y. (2021) · theses.fr (ABES) · doi:10.70675/d6386e02z3b20z4c4bza6e2z7ea885aa66d9

Effect of gut microbiota from children with autism spectrum disorder (ASD) on behavior and ASD-related biological markers in germ-free mice

Roussin, L. (2023) · theses.fr (ABES) · doi:10.70675/998d3bd1z4618z400dz998cz89e524b35aef · Cited by 1

Place de la diversité bactérienne et de sa dynamique dans la surveillance épidémiologique

Kaba, L. (2022) · theses.fr (ABES) · doi:10.70675/5f00cf1fzdaa3z41e8zbb90ze22cb93d4b5b

Peyer’s patch immune response during malnutrition and infection by Salmonella enterica Typhimurium

Hidalgo-Villeda, F. (2022) · theses.fr (ABES) · doi:10.70675/981ec17dz4d78z44e3za178zc9a677670d20

Crosstalk between the microbiome and the mucosal immunoglobulin A system in the lung, in health and disease

Stavart, C., Gohy, S., Lebeer, S., Françoise Van Bambeke, A., Crabbé, A., & Pilette, C. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1796523

Gut microbiota translocation and dissemination in health: can it be beneficial and purposeful?

Udayan, S., Martín, A. P., & Newberry, R. D. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2662740

Compositional maturation of the microbiome and adaptive immunity in the postnatal period

Green, M., Cleary, S. R., Kwiecien-Delaney, B. J., & Foster (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1772425

Early-life Wnt4 expressing colon stromal cells orchestrate lifelong mucosal homeostasis via BMP-driven iNKT cell imprinting

Lin, X., Lee, C. H.-J., Zhang, T., Antanaviciute, A., Hanley, T., Glickman, J. N., Bharadwaj, N. S. S., Rosen, V., Gumperz, J. E., Waldor, M. K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72734-9

Postnatal Reprogramming Shapes Human Intestinal Epithelial Immune CompetencyPreprint

Lee, C. H.-J., Fawkner-Corbett, D., Christoforidou, Z., Gerós, A. S., Lentsch, V., Sheikh, L., Bridges, E., Jagielowicz, M., Deng, L., Qin, X., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.05.722861

Comparative Analysis of Fecal Microbiome Composition in Zoo‐Housed Colobines: The Influence of Dietary Macronutrients, Browse Provisioning, and Phylogeny

Plocek, M. R., Dunham, N. T., & Amato, K. R. (2026) · American Journal of Primatology · doi:10.1002/ajp.70169

The Inflammatory Response in the Murine Ovalbumin‐Induced Skin Inflammation Model Is Robust Despite Major Gut Microbiota Differences

Henriksen, I. W., Bartholdy, C., Koch, J., Stefanova, D. V., Hansen, C. H. F., & Hansen, A. K. (2026) · Clinical and Translational Science · doi:10.1111/cts.70593

Gut microbiota from health to disease: A role for biofilms?

Buret, A. G., & Allain, T. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40306-4.00011-9

Perinatal antibiotics in a db/db mouse model impact obesity and hyperglycemia in a microbiome-dependent manner

Curtis-Joseph, N., Laubi, A. J., Campa, M. O. A. D. L., & Belenky, P. A. (2026) · Frontiers in Microbiomes · doi:10.3389/frmbi.2026.1750320

Epidural‐Related Maternal Fever Is Associated With Structural Alterations in Vaginal Floral Homeostasis Among Parturients

Xiong, C., Chen, X., Zhai, W., & Zhang, X. (2026) · Obstetrics and Gynecology International · doi:10.1155/ogi/7458179

A temporal differentiation program after birth delineates γδ T cell immunity

Baglioni, M. V., da Silva, M. G. F. F., Sonnenholzner, A., Rizk, J., Copland, A., Tardos, E. C., Secci, D., Sebastián, P. P., Laursen, M. F., Kappel, S. S., et al. (2026) · Science Advances · doi:10.1126/sciadv.aee6790

Incidence rates of allergy diagnoses in the U.S. military health system after the COVID-19 pandemic

Brough, J. J., Berill, Z., Susi, A., Sanchez, E. P., Schwartz, D., Nylund, C. M., & Mitre, E. E. S. (2026) · Frontiers in Allergy · doi:10.3389/falgy.2026.1884771

Natural microbiota confer life-long protection against obesity via an early-life, immune-mediated effect on brown adipocytes

Azar, S., Gavrilova, O., Baker, G., Oh, J. H., Fukutomi, K., Seishima, J., Ma, J., Kwak, M., Badger, J. H., Trinchieri, G., et al. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2718613

Microbial epigenetic regulation as a multilevel regulatory interface in host-microbe interactions

Yizengaw, L., & Wang, G.-H. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2725428 · Cited by 1

Bacteria-induced immunity: from homeostasis to immune subversion in periodontitis

Miranda, V. L., Teixeira, M. D. A., Souza, J. G. S., Bezinelli, L. M., & dos Santos, N. C. C. (2026) · Einstein (São Paulo) · doi:10.31744/einstein_journal/2026rw2369

From gut microbiota dysbiosis to immune dysregulation: pathogenic mechanisms and emerging therapeutic perspectives in pediatric asthma

Liu, Z., Yu, K., Gao, J., Zhang, T., Liu, F., & Zhuang, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1901737

From gut to lung: the microbiome-directed causal mechanisms and therapeutic horizons in asthma

Ni, F.-X., Pan, C. F., Chen, H.-H., Huang, D.-H., & Jiang, Z.-B. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1935791

Association of gut microbiota and regulatory T cells with vaccine immunogenicity in HIV-exposed uninfected and HIV-unexposed infants: a longitudinal cohort study

Johnson, M. J., Frank, D. N., Tovar-Salazar, A., Nunes, M. C., Madhi, S. A., & Weinberg, A. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106500

The microbiota, a necessary element of immunity

Eberl, G. (2018) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2018.03.003 · Cited by 17

Early life microbiome influences on development of the mucosal innate immune system

Ignácio, A., Czyz, S., & McCoy, K. D. (2024) · Seminars in Immunology · doi:10.1016/j.smim.2024.101885 · Cited by 55

The early life education of the immune system: Moms, microbes and (missed) opportunities

Jain, N. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1824564 · Cited by 119

Chapter 6 The intestinal microbiota and the child’s immune system

Jenmalm, M. C., & Prescott, S. L. (2017) · Wageningen Academic Publishers eBooks · doi:10.3920/978-90-8686-839-1_6 · Cited by 3

A mother's touch: microbial guardians of early immune imprinting

Zeng, M. Y., & Brown, J. A. (2025) · Trends in Immunology · doi:10.1016/j.it.2025.09.008 · Cited by 3