The microbiome and innate immunity

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444

Diversity of the Human Intestinal Microbial Flora

Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913

Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease

Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662

Intestinal microbiota metabolism of l-carnitine, a nutrient in red meat, promotes atherosclerosis

Koeth, R. A., Wang, Z., Levison, B. S., Buffa, J. A., Org, E., Sheehy, B. T., Britt, E. B., Fu, X., Wu, Y., Li, L., et al. (2013) · Nature Medicine · doi:10.1038/nm.3145 · Cited by 4,386

Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis

Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251

Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy

Sivan, A., Corrales, L., Hubert, N., Williams, J. B., Aquino-Michaels, K., Earley, Z. M., Benyamin, F. W., Man Lei, Y., Jabri, B., Alegre, M.-L., et al. (2015) · Science · doi:10.1126/science.aac4255 · Cited by 3,888

Type 2 diabetes as an inflammatory disease

Donath, M. Y., & Shoelson, S. E. (2011) · Nature Reviews Immunology · doi:10.1038/nri2925 · Cited by 3,737

Intestinal dendritic cell licensing through Toll-like receptor 4 is required for oral tolerance in allergic contact dermatitis

Hacini‐Rachinel, F., de Agüero, M. G., Kanjarawi, R., Moro-Sibilot, L., Luduec, J.-B. L., Macari, C., Boschetti, G., Bardel, É., Langella, P., Dubois, B., et al. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.02.022 · Cited by 30

Role of toll-like receptor 4 (TLR4)-mediated interleukin-6 (IL-6) production in chemotherapy-induced mucositis

Khan, S., Wardill, H. R., & Bowen, J. M. (2018) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-018-3605-9 · Cited by 30

The impacts of oral and gut microbiota on alveolar bone loss in periodontitis

Han, N., Li, X., Du, J., Xu, J., Guo, L., & Liu, Y. F. (2023) · Journal of Periodontal Research · doi:10.1111/jre.13168 · Cited by 30

Gut dysbiosis-related thrombosis in inflammatory bowel disease: Potential disease mechanisms and emerging therapeutic strategies

Papa, A., Santini, P., Lucia, S. S. D., Maresca, R., Porfidia, A., Pignatelli, P., Gasbarrini, A., Violi, F., & Pola, R. (2023) · Thrombosis Research · doi:10.1016/j.thromres.2023.11.005 · Cited by 29

NEDD4L mediates intestinal epithelial cell ferroptosis to restrict inflammatory bowel diseases and colorectal tumorigenesis

Liang, J., Wang, N., Yao, Y., Wang, Y., An, X., Wang, H., Liu, H., Jiang, Y., Li, H., Cheng, X., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci173994 · Cited by 29

Complex Gastrointestinal and Endocrine Sources of Inflammation in Schizophrenia

Severance, E. G., Dickerson, F., & Yolken, R. H. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00549 · Cited by 29

Administration of Saccharomyces boulardii mafic-1701 improves feed conversion ratio, promotes antioxidant capacity, alleviates intestinal inflammation and modulates gut microbiota in weaned piglets

Zhang, W., Bao, C., Wang, J., Zang, J., & Cao, Y. (2020) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-020-00516-4 · Cited by 31

The Associations between Diet and Socioeconomic Disparities and the Intestinal Microbiome in Preadolescence

Lapidot, Y., Reshef, L., Goldsmith, R., Na’amnih, W., Kassem, E., Ornoy, A., Gophna, U., & Muhsen, K. (2021) · Nutrients · doi:10.3390/nu13082645 · Cited by 29

Habitat Disturbance Linked with Host Microbiome Dispersion and Bd Dynamics in Temperate Amphibians

Neely, W. J., Greenspan, S. E., Stahl, L. M., Heraghty, S. D., Marshall, V. M., Atkinson, C. L., & Becker, C. G. (2021) · Microbial Ecology · doi:10.1007/s00248-021-01897-3 · Cited by 29

Effects of exposure to cadmium (Cd) and selenium-enriched Lactobacillus plantarum in Luciobarbus capito: Bioaccumulation, antioxidant responses and intestinal microflora

Shang, X., Xu, W., Zhao, Z., Luo, L., Zhang, Q., Li, M., Sun, Q., & Geng, L. (2022) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2022.109352 · Cited by 29

Effect of the Microbiome on Intestinal Innate Immune Development in Early Life and the Potential Strategy of Early Intervention

Yang, Z., Liu, X., Wu, Y., Peng, J., & Wei, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.936300 · Cited by 33

Endometriosis biomarkers of the disease: an update

Soto, D. E., Rassier, S. L. C., Green, I. C., Burnett, T. L., Khan, Z., & Cope, A. G. (2022) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0000000000000798 · Cited by 29

Microbiome in cancer: An exploration of carcinogenesis, immune responses and immunotherapy

Zhou, P., Hu, Y., Wang, X., Shen, L., Liao, X., Zhu, Y., Yu, J., Zhao, F., Zhou, Y., Shen, H., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.877939 · Cited by 31

The relationship between atrial fibrillation and NLRP3 inflammasome: a gut microbiota perspective

Xing, Y., Yan, L., Li, X., Xu, Z., Wu, X., Gao, H., Chen, Y., Ma, X., Liu, J., & Zhang, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1273524 · Cited by 29

Nanotechnology Applications in Breast Cancer Immunotherapy

Wang, R., Kumar, P., Reda, M. M., Wallstrum, A., Crumrine, N. A., Ngamcherdtrakul, W., & Yantasee, W. (2023) · Small · doi:10.1002/smll.202308639 · Cited by 30

Bioactives and their roles in bone metabolism of osteoarthritis: evidence and mechanisms on gut-bone axis

Basak, S., Hridayanka, K. S. N., & Duttaroy, A. K. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1323233 · Cited by 29

Usual Consumption of Specific Dairy Foods Is Associated with Breast Cancer in the Roswell Park Cancer Institute Data Bank and BioRepository

McCann, S. E., Hays, J., Baumgart, C., Weiss, E. H., Yao, S., & Ambrosone, C. B. (2017) · Current Developments in Nutrition · doi:10.3945/cdn.117.000422 · Cited by 29

The Intra-Dependence of Viruses and the Holobiont

Grasis, J. A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01501 · Cited by 30

Production of a Functional Factor, p40, by Lactobacillus rhamnosus GG Is Promoted by Intestinal Epithelial Cell-Secreted Extracellular Vesicles

Yang, L., Higginbotham, J. N., Liu, L., Zhao, G., Acra, S. A., Peek, R. M., Polk, D. B., Li, H., & Yan, F. (2019) · Infection and Immunity · doi:10.1128/iai.00113-19 · Cited by 29

Understanding the immunological interactions of engineered nanomaterials: Role of the bio‐corona

Fadeel, B. (2022) · Wiley Interdisciplinary Reviews Nanomedicine and Nanobiotechnology · doi:10.1002/wnan.1798 · Cited by 29

The microbiome and the gut-lung axis in tuberculosis: interplay in the course of disease and treatment

Alvarado-Peña, N., Galeana-Cadena, D., Gómez-García, I. A., Mainero, X. S., & Silva‐Herzog, E. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1237998 · Cited by 29

Antibiotic-induced gut microbiome perturbation alters the immune responses to the rabies vaccine

Feng, Y., de Jong, S. E., Oliveira, A. P. B. N., Samaha, H., Yang, F., Hu, M., Wang, Y., Beydoun, N., Xie, X., Zhang, H., et al. (2025) · Cell Host & Microbe · doi:10.1016/j.chom.2025.03.015 · Cited by 31

Prophylactic efficacy of orally administered Bacillus poly-γ-glutamic acid, a non-LPS TLR4 ligand, against norovirus infection in mice

Lee, W., Kim, M., Lee, S., Jung, H.-G., & Oh, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-26935-y · Cited by 28

Bacterial Diversity in the Intestinal Mucosa of Dysbiosis Diarrhea Mice Treated with Qiweibaizhu Powder

Long, C., Shao, H., Luo, C., Yu, R., & Tan, Z. (2020) · Gastroenterology Research and Practice · doi:10.1155/2020/9420129 · Cited by 28

From Nursery to Nursing Home: Emerging Concepts in Clostridioides difficile Pathogenesis

Smith, A. B., Ocaña, J. S., & Zackular, J. P. (2020) · Infection and Immunity · doi:10.1128/iai.00934-19 · Cited by 31

Intestinal protozoan infections shape fecal bacterial microbiota in children from Guinea-Bissau

von Huth, S., Thingholm, L. B., Kofoed, P., Bang, C., Rühlemann, M. C., Franke, A., & Holmskov, U. (2021) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0009232 · Cited by 28

Multi-walled carbon nanotube polysaccharide modified Hericium erinaceus polysaccharide as an adjuvant to extend immune responses

Ren, Z., Luo, Y., Meng, Z., Zhang, J., Yu, R., Sun, M., Xu, T., Li, J., Ma, Y., Huang, Y., et al. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.03.180 · Cited by 28

Shades of grey: host phenotype dependent effect of urbanization on the bacterial microbiome of a wild mammal

Stothart, M. R., & Newman, A. E. M. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00105-4 · Cited by 30

Fibroblast membrane-camouflaged nanoparticles for inflammation treatment in the early stage

Sun, L., He, L., Wu, W., Luo, L., Han, M., Liu, Y., Shi, S., Zhong, K., Yang, J., & Li, J. (2021) · International Journal of Oral Science · doi:10.1038/s41368-021-00144-2 · Cited by 28

Translocation of Helicobacter hepaticus synergizes with myeloid-derived suppressor cells and contributes to breast carcinogenesis

Deng, H., Muthupalani, S., Erdman, S. E., Liu, H., Niu, Z., Wang, T. C., & Fox, J. G. (2022) · OncoImmunology · doi:10.1080/2162402x.2022.2057399 · Cited by 28

Multi-Omics Integration Reveals the Crucial Role of Fusobacterium in the Inflammatory Immune Microenvironment in Head and Neck Squamous Cell Carcinoma

Qiao, H., Li, H., Wen, X.-H., Tan, X.-R., Yang, C., & Liu, N. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01068-22 · Cited by 28

Mesenchymal stem cells ( MSCs ) and MSC ‐derived exosomes in animal models of central nervous system diseases: Targeting the NLRP3 inflammasome

Nazari, S., Pourmand, S. M., Motevaseli, E., & Hassanzadeh, G. (2023) · IUBMB Life · doi:10.1002/iub.2759 · Cited by 29

Qualitative and Quantitative DNA- and RNA-Based Analysis of the Bacterial Stomach Microbiota in Humans, Mice, and Gerbils

Wurm, P., Dörner, E., Kremer, C., Spranger, J., Maddox, C., Halwachs, B., Harrison, U., Blanchard, T. G., Haas, R., Högenauer, C., et al. (2018) · mSystems · doi:10.1128/msystems.00262-18 · Cited by 30

Fecal microbiota of different reproductive stages of the central population of the lesser-long nosed bat, Leptonycteris yerbabuenae

Gaona, O., Gómez-Acata, S., Cerqueda‐García, D., Neri-Barrios, C. X., & Falcón, L. I. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219982 · Cited by 29

Oral and intestinal microbial features in pregnant women with hypothyroidism and their correlations with pregnancy outcomes

Wang, B., Xu, Y., Zhang, M., Zhang, J., Hou, X., Li, J., Cai, Y., Sun, Z., Ban, Y., & Wang, W. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00234.2020 · Cited by 28

Gut microbiome on immune checkpoint inhibitor therapy and consequent immune-related colitis: a review

Hwang, S. W., Kim, M. K., & Kweon, M. (2023) · Intestinal Research · doi:10.5217/ir.2023.00019 · Cited by 28

AllergoOncology: Microbiota in allergy and cancer—A European Academy for Allergy and Clinical Immunology position paper

Untersmayr, E., Bax, H. J., Bergmann, C., Bianchini, R., Cozen, W., Gould, H. J., Hartmann, K., Josephs, D. H., Levi‐Schaffer, F., Penichet, M. L., et al. (2019) · Allergy · doi:10.1111/all.13718 · Cited by 27

Exposure of the Host-Associated Microbiome to Nutrient-Rich Conditions May Lead to Dysbiosis and Disease Development—an Evolutionary Perspective

Lachnit, T., Bosch, T. C. G., & Deines, P. (2019) · mBio · doi:10.1128/mbio.00355-19 · Cited by 29

The Activation of Mucosal-Associated Invariant T (MAIT) Cells Is Affected by Microbial Diversity and Riboflavin Utilization in vitro

Krause, J. L., Schäpe, S. S., Schattenberg, F., Müller, S., Ackermann, G., Rolle-Kampczyk, U. E., Jehmlich, N., Pierzchalski, A., von Bergen�, M., & Herberth, G. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00755 · Cited by 29

Regulation of axial and head patterning during planarian regeneration by a commensal bacterium

Williams, K. B., Bischof, J., Lee, F. J., Miller, K. A., LaPalme, J. V., Wolfe, B. E., & Levin, M. G. (2020) · Mechanisms of Development · doi:10.1016/j.mod.2020.103614 · Cited by 27

Microbiome as a Target for Cancer Therapy

Suraya, R., Nagano, T., Kobayashi, K., & Nishimura, Y. (2020) · Integrative Cancer Therapies · doi:10.1177/1534735420920721 · Cited by 27

Effects of changes on gut microbiota in children with acute Kawasaki disease

Shen, J., Ding, Y., Yang, Z., Zhang, X., & Zhao, M. (2020) · PeerJ · doi:10.7717/peerj.9698 · Cited by 27

The gut microbiome in solid organ transplantation

Arassi, M. B., Zeller, G., Karcher, N., Zimmermann, M., & Tönshoff, B. (2020) · Pediatric Transplantation · doi:10.1111/petr.13866 · Cited by 27

Innate Immune Responses and Gut Microbiomes Distinguish HIV-Exposed from HIV-Unexposed Children in a Population-Specific Manner

Amenyogbe, N., Dimitriu, P. A., Cho, P., Ruck, C. E., Fortuno, E. S., Cai, B., Alimenti, A., Côté, H. C. F., Maan, E. J., Slogrove, A. L., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000040 · Cited by 27

Gut Microbiota, Peroxisome Proliferator-Activated Receptors, and Hepatocellular Carcinoma

Yu, Q., Wu, L., Ji, J., Feng, J., Dai, W., Li, J., Wu, J., & Guo, C. (2020) · Journal of Hepatocellular Carcinoma · doi:10.2147/jhc.s277870 · Cited by 27

The microbiome and the immune system in critical illness

Miniet, A. A., Grunwell, J. R., & Coopersmith, C. M. (2021) · Current Opinion in Critical Care · doi:10.1097/mcc.0000000000000800 · Cited by 27

Beyond classic concepts in thyroid homeostasis: Immune system and microbiota

Fernández-García, V., González-Ramos, S., Martín‐Sanz, P., Laparra, J. M., & Boscá, L. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111333 · Cited by 27

Bacterial community dynamics on bats and the implications for pathogen resistance

Li, A., Li, Z., Dai, W., Parise, K. L., Leng, H., Jin, L., Liu, S., Sun, K., Hoyt, J. R., & Feng, J. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15754 · Cited by 27

MAIT cell activation is reduced by direct and microbiota-mediated exposure to bisphenols

Krause, J. L., Engelmann, B., da Rocha, U. N., Pierzchalski, A., Chang, H., Zenclussen, A. C., von Bergen�, M., Rolle-Kampczyk, U. E., & Herberth, G. (2021) · Environment International · doi:10.1016/j.envint.2021.106985 · Cited by 28

Crosstalk between the gut microbiome and clinical response in locally advanced thoracic esophageal squamous cell carcinoma during neoadjuvant camrelizumab and chemotherapy

Xu, L., Qi, Y., Jiang, Y., Ji, Y., Zhao, Q., Wu, J., Lu, W., Wang, Y., Chen, Q., & Wang, C. (2022) · Annals of Translational Medicine · doi:10.21037/atm-22-1165 · Cited by 27

Symbiosis: the other cells in development

Carrier, T. J., & Bosch, T. C. G. (2022) · Development · doi:10.1242/dev.200797 · Cited by 29

The gut microbiota contributes to changes in the host immune response induced by Trichinella spiralis

Li, C.-Y., Liu, Y., Liu, X., Bai, X., Jin, X., Xu, F., Chen, H., Zhang, Y., Vallée, I., Liu, M., et al. (2023) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0011479 · Cited by 28

Cholecystectomy Significantly Alters Gut Microbiota Homeostasis and Metabolic Profiles: A Cross-Sectional Study

Xu, F., Chen, R., Zhang, C., Wang, H., Ding, Z., Yu, L., Tian, F., Chen, W., Zhou, Y., & Zhai, Q. (2023) · Nutrients · doi:10.3390/nu15204399 · Cited by 31

Hybrid Cell Membrane‐Based Nanoplatforms for Enhanced Immunotherapy against Cancer and Infectious Diseases

Peng, X., Li, Y., Yuan, P., & Ding, X. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202304477 · Cited by 27

A Perspective Discussion on Rising Pesticide Levels and Colon Cancer Burden in Brazil

Uyemura, S. A., Stopper, H., Martin, F. L., & Kannen, V. (2017) · Frontiers in Public Health · doi:10.3389/fpubh.2017.00273 · Cited by 27

Development of a Safe and Effective Vaccinia Virus Oncolytic Vector WR-Δ4 with a Set of Gene Deletions on Several Viral Pathways

Mejías‐Pérez, E., Carreño‐Fuentes, L., & Estéban, M. (2017) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2017.12.002 · Cited by 27

IL-1R and MyD88 Contribute to the Absence of a Bacterial Microbiome on the Healthy Murine Cornea

Wan, S. J., Sullivan, A. B., Shieh, P., Metruccio, M. M. E., Evans, D. J., Bertozzi, C. R., & Fleiszig, S. M. J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01117 · Cited by 28

Echinococcus granulosus Infection Results in an Increase in Eisenbergiella and Parabacteroides Genera in the Gut of Mice

Bao, J., Zheng, H., Wang, Y., Zheng, X., Li, H., Qi, W., Wang, T., Guo, B., Guo, G., Zhang, Z., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02890 · Cited by 27

Microbiota determines insulin sensitivity in TLR2-KO mice

Guadagnini, D., Rocha, G. Z., Santos, A., Assalin, H. B., Hirabara, S. M., Curi, R., Oliveira, A. G., Prada, P. O., & Saad, M. J. A. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116793 · Cited by 27

The Dutch Microbiome Project defines factors that shape the healthy gut microbiomePreprint

Gaćeša, R., Kurilshikov, A., Vila, A. V., Sinha, T., Klaassen, M. A. Y., Bolte, L. A., Andreu‐Sánchez, S., Chen, L., Collij, V., Hu, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.27.401125 · Cited by 27

Perturbations of the ocular surface microbiome and their effect on host immune function

Chang, C.-C. J., & Winn, B. J. (2022) · Current Opinion in Ophthalmology · doi:10.1097/icu.0000000000000931 · Cited by 26

Genetic predisposition of the gastrointestinal microbiome and primary biliary cholangitis: a bi-directional, two-sample Mendelian randomization analysis

Luo, X., & You, X. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1225742 · Cited by 26

Kidney transplantation and gut microbiota

Chen, Z. W., Chang, X., Ye, Q., Gao, Y., & Deng, R. (2024) · Clinical Kidney Journal · doi:10.1093/ckj/sfae214 · Cited by 26

The Hologenome Concept of Evolution: Medical Implications

ROSENBERG, E. B., & Zilber‐Rosenberg, I. (2019) · Rambam Maimonides Medical Journal · doi:10.5041/rmmj.10359 · Cited by 28

Microbiota Inhibit Epithelial Pathogen Adherence by Epigenetically Regulating C-Type Lectin Expression

Woo, V., Eshleman, E. M., Rice, T., Whitt, J., Vallance, B. A., & Alenghat, T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00928 · Cited by 27

Co-infection of Malassezia sympodialis With Bacterial Pathobionts Pseudomonas aeruginosa or Staphylococcus aureus Leads to Distinct Sinonasal Inflammatory Responses in a Murine Acute Sinusitis Model

Lee, K., Zhang, I., Kyman, S., Kask, O., & Cope, E. K. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00472 · Cited by 26

Associations of faecal microbiota with influenza-like illness in participants aged 60 years or older: an observational study

Fuentes, S., den Hartog, G., Nanlohy, N. M., Wijnands, L. M., Ferreira, J. A., Nicolaie, M. A., Pennings, J. L. A., Jacobi, R. H. J., de Wit, J., van Beek, J., et al. (2021) · The Lancet Healthy Longevity · doi:10.1016/s2666-7568(20)30034-9 · Cited by 28

Biomolecular Mechanisms of Autoimmune Diseases and Their Relationship with the Resident Microbiota: Friend or Foe?

Topi, S., Bottalico, L., Charitos, I. A., Colella, M., Domenico, M. D., Palmirotta, R., & Santacroce, L. (2022) · Pathophysiology · doi:10.3390/pathophysiology29030041 · Cited by 26

Manganese enhances DNA- or RNA-mediated innate immune response by inducing phosphorylation of TANK-binding kinase 1

Sui, H., Chen, Q., Yang, J., Srirattanapirom, S., & Imamichi, T. (2022) · iScience · doi:10.1016/j.isci.2022.105352 · Cited by 27

Underlying beneficial effects of Rhubarb on constipation-induced inflammation, disorder of gut microbiome and metabolism

Gao, H., He, C., Hua, R., Chen, L., Wang, B., Du, Y., Xin, S., Guo, Y., Gao, L., Zhang, L., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1048134 · Cited by 26

Targeting the gut microbiota to alleviate chemotherapy-induced toxicity in cancer

Xu, Y., Du, H., Chen, Y., Ma, C., Zhang, Q., Li, H., Xie, Z., & Hong, Y. (2023) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2023.2233605 · Cited by 27

Repression of Salmonella Host Cell Invasion by Aromatic Small Molecules from the Human Fecal Metabolome

Peixoto, R. J. M., Alves, E. S., Wang, M., Ferreira, R. B. R., Granato, A., Han, J., Gill, H., Jacobson, K., Lobo, L. A., Domingues, R. M. C. P., et al. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01148-17 · Cited by 26

Intestinal Microbiota in Sepsis

Sun, T., Wang, L., & Zhang, H. (2022) · Intensive Care Research · doi:10.1007/s44231-022-00001-8 · Cited by 26

Bacteria-based biohybrids for remodeling adenosine-mediated immunosuppression to boost radiotherapy-triggered antitumor immune response

Wu, X., Zhang, J., Deng, Z., Sun, X., Zhang, Y., Zhang, C., Wang, J., Yu, X., & Yang, G. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.123000 · Cited by 25

The gut microbiota: an emerging modulator of drug resistance in hepatocellular carcinoma

Yao, J., Ning, B., & Ding, J. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2473504 · Cited by 26

Nonmicrobicidal Small Molecule Inhibition of Polysaccharide Metabolism in Human Gut Microbes: A Potential Therapeutic Avenue

Santilli, A. D., Dawson, E. M., Whitehead, K. J., & Whitehead, D. C. (2018) · ACS Chemical Biology · doi:10.1021/acschembio.8b00309 · Cited by 25

The clinical implications of the microbiome in the development of allergy diseases

Koidl, L., & Untersmayr, E. (2021) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2021.1874353 · Cited by 25

Do Engineered Nanomaterials Affect Immune Responses by Interacting With Gut Microbiota?

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Microbiome and Gut Immunity: Innate Immune Cells

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