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

The role of gut microbiota and its metabolites short-chain fatty acids in food allergy

Chen, C., Liu, C., Zhang, K., & Xue, W. (2022) · Food Science and Human Wellness · doi:10.1016/j.fshw.2022.09.003 · Cited by 61

Pathophysiology of Intestinal Na+/H+ Exchange

Gurney, M. A., Laubitz, D., Ghishan, F. K., & Kiela, P. R. (2016) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2016.09.010 · Cited by 60

The gut microbiota: A new potential driving force in liver cirrhosis and hepatocellular carcinoma

Sanduzzi‐Zamparelli, M., Rocco, A., Compare, D., & Nardone, G. (2017) · United European Gastroenterology Journal · doi:10.1177/2050640617705576 · Cited by 60

Significance of human microbiome in breast cancer: Tale of an invisible and an invincible

Chadha, J., Nandi, D., Atri, Y., & Nag, A. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.07.010 · Cited by 60

Predigestion as an Evolutionary Impetus for Human Use of Fermented Food

Amato, K. R., Mallott, E. K., Maia, P. D., & Sardaro, M. L. S. (2021) · Current Anthropology · doi:10.1086/715238 · Cited by 63

A heterogenic membrane-based biomimetic hybrid nanoplatform for combining radiotherapy and immunotherapy against breast cancer

Pan, P., Dong, X., Chen, Y., Ye, J., Sun, Y., & Zhang, X. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121810 · Cited by 59

T helper 17 (Th17) cell responses to the gut microbiota in human diseases

Sun, C., Yang, N. Y., Zheng, Z., Liu, D., & Xu, Q. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114483 · Cited by 60

Limosilactobacillus mucosae-derived extracellular vesicles modulates macrophage phenotype and orchestrates gut homeostasis in a diarrheal piglet model

Li, J., Feng, S., Wang, Z., He, J., Zhang, Z., Zou, H., Wu, Z., Liu, X., Hong Kui, W. E. I., & Tao, S. (2023) · npj Biofilms and Microbiomes · doi:10.1038/s41522-023-00403-6 · Cited by 61

A Cardiolipin from Muribaculum intestinale Induces Antigen-Specific Cytokine Responses

Bang, S., Shin, Y., Ma, X., Park, S., Graham, D. B., Xavier, R. J., & Clardy, J. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c09734 · Cited by 60

Bacterial extracellular vesicles at the interface of gut microbiota and immunity

Melo-Marques, I., Cardoso, S. M., & Empadinhas, N. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2396494 · Cited by 61

Nanosized Drug Delivery Systems in Gastrointestinal Targeting: Interactions with Microbiota

Karavolos, M. H., & Holban, A. M. (2016) · Pharmaceuticals · doi:10.3390/ph9040062 · Cited by 61

‘RA and the microbiome: do host genetic factors provide the link?

Wells, P. M., Williams, F. M. K., Matey-Hernandez, M. L., Menni, C., & Steves, C. J. (2019) · Journal of Autoimmunity · doi:10.1016/j.jaut.2019.02.004 · Cited by 59

Titanium dioxide nanoparticles via oral exposure leads to adverse disturbance of gut microecology and locomotor activity in adult mice

Zhang, S., Jiang, X., Cheng, S., Fan, J., Qin, X., Wang, T., Zhang, Y., Zhang, J., Qiu, Y. L., Qiu, J., et al. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02698-2 · Cited by 61

Regulation of cGAS‐Mediated Immune Responses and Immunotherapy

Saeed, A. F. U. H., Ruan, X., Guan, H., Su, J., & Ouyang, S. (2020) · Advanced Science · doi:10.1002/advs.201902599 · Cited by 60

Immunogenetic variation shapes the gut microbiome in a natural vertebrate population

Davies, C. S., Worsley, S. F., Maher, K. H., Komdeur, J., Burke, T. A., Dugdale, H. L., & Richardson, D. S. (2022) · Microbiome · doi:10.1186/s40168-022-01233-y · Cited by 59

Research progress on prevention and treatment of glucolipid metabolic disease with integrated traditional Chinese and Western medicine

Guo, J. (2017) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-017-2811-3 · Cited by 58

Prophylactic probiotics for cancer therapy-induced diarrhoea: a meta-analysis

Wardill, H. R., Sebille, Y. Z. A. V., Ciorba, M. A., & Bowen, J. M. (2018) · Current Opinion in Supportive and Palliative Care · doi:10.1097/spc.0000000000000338 · Cited by 59

Iron deficiency anemia-related gut microbiota dysbiosis in infants and young children: A pilot study

Mulevičienė, A., D’Amico, F., Turroni, S., Candela, M., & Jankauskienė, A. (2018) · Acta Microbiologica et Immunologica Hungarica · doi:10.1556/030.65.2018.045 · Cited by 60

Use of vitamin/zinc supplements, medicinal plants, and immune boosting drinks during COVID-19 pandemic: A pilot study from Benha city, Egypt

Khabour, O. F., & Hassanein, S. F. M. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e06538 · Cited by 57

The Use of Fecal Microbiome Transplant in Treating Human Diseases: Too Early for Poop?

Ser, H., Letchumanan, V., Goh, B. H., Wong, S. H., & Lee, L. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.519836 · Cited by 57

MiRNAs and lncRNAs in the regulation of innate immune signaling

Фанилевич, Г. И., Ramírez, M. D. J. E., Goncharov, E. N., Ivliev, D., Shumadalova, A. V., Ilyasova, T., & Wang, C. (2023) · Non-coding RNA Research · doi:10.1016/j.ncrna.2023.07.002 · Cited by 57

Nanoparticles for immune system targeting

Du, J., Zhang, Y. S., Hobson, D., & Hydbring, P. (2017) · Drug Discovery Today · doi:10.1016/j.drudis.2017.03.013 · Cited by 57

Effects of long-term intake of a yogurt fermented with Lactobacillus delbrueckii subsp. bulgaricus 2038 and Streptococcus thermophilus 1131 on mice

Usui, Y., Kimura, Y., Satoh, T., Takemura, N., Ouchi, Y., Hiroko, O., KOBAYASHI, K., Suzuki, H., Satomi, K., Hagiwara, S., et al. (2018) · International Immunology · doi:10.1093/intimm/dxy035 · Cited by 57

Differential responses of gut microbiota of male and female fathead minnow (Pimephales promelas) to a short-term environmentally-relevant, aqueous exposure to benzo[a]pyrene

DeBofsky, A., Xie, Y., Grimard, C., Alcaraz, A. J., Brinkmann, M., Hecker, M., & Giesy, J. P. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.126461 · Cited by 60

The impact of a high fat diet on bones: potential mechanisms

Qiao, J., Wu, Y., & Ren, Y. (2020) · Food & Function · doi:10.1039/d0fo02664f · Cited by 57

Immune Privilege: The Microbiome and Uveitis

Mölzer, C., Heissigerová, J., Wilson, H. M., Kuffová, L., & Forrester, J. V. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.608377 · Cited by 59

Update: Innate Lymphoid Cells in Inflammatory Bowel Disease

Luo, W., Tian, L., Tan, B., Shen, Z., Xiao, M., Wu, S., Meng, X., Wu, X., & Wang, X. (2021) · Digestive Diseases and Sciences · doi:10.1007/s10620-021-06831-8 · Cited by 56

Cancer-associated inflammation: pathophysiology and clinical significance

Pęczek, P., Gajda, M., Rutkowski, K., Fudalej, M. M., Deptała, A., & Badowska-Kozakiewicz, A. M. (2022) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-022-04399-y · Cited by 57

Cloaking Mesoporous Polydopamine with Bacterial Membrane Vesicles to Amplify Local and Systemic Antitumor Immunity

Chen, W., Song, Y., Bai, S., He, C., Guo, Z., Zhu, Y., Zhang, Z., & Sun, X. (2023) · ACS Nano · doi:10.1021/acsnano.3c00363 · Cited by 57

Fecal virome transplantation is sufficient to alter fecal microbiota and drive lean and obese body phenotypes in mice

Borin, J. M., Liu, R., Wang, Y., Wu, T., Chopyk, J., Huang, L., Kuo, P., Ghose, C., Meyer, J. R., Tu, X. M., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2236750 · Cited by 58

Microbiome control of innate reactivity

Chen, F., & Stappenbeck, T. S. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.12.003 · Cited by 57

Gut Microbiota and Probiotics/Synbiotics for Modulation of Immunity in Critically Ill Patients

Shimizu, K., Ojima, M., & Ogura, H. (2021) · Nutrients · doi:10.3390/nu13072439 · Cited by 56

Metabolic regulation on the immune environment of glioma through gut microbiota

Lyu, Y., Yang, H., & Liang, C. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.05.005 · Cited by 55

The gut microbiome as a biomarker of differential susceptibility to SARS-CoV-2

Sarkar, A., Harty, S., Moeller, A. H., Klein, S. L., Erdman, S. E., Friston, K. J., & Carmody, R. N. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.09.009 · Cited by 56

Modulation of Dendritic Cells by Microbiota Extracellular Vesicles Influences the Cytokine Profile and Exosome Cargo

Díaz‐Garrido, N., Badı́a, J., & Baldomà, L. (2022) · Nutrients · doi:10.3390/nu14020344 · Cited by 55

Regulation of bile acid metabolism-related signaling pathways by gut microbiota in diseases

Jia, E., Liu, Z.-Y., Pan, M., Lu, J., & Ge, Q. (2019) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1900073 · Cited by 55

Exploring the Potential Role of the Gut Microbiome in Chemotherapy-Induced Neurocognitive Disorders and Cardiovascular Toxicity

Čierniková, S., Mego, M., & Chovanec, M. (2021) · Cancers · doi:10.3390/cancers13040782 · Cited by 55

Alteration of the gut microbiota and metabolite phenylacetylglutamine in patients with severe chronic heart failure

Zhang, Z., Cai, B., Sun, Y., Deng, H., Wang, H., & Qiao, Z. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.1076806 · Cited by 58

The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice

Asseri, A. H., Bakhsh, T., Abuzahrah, S. S., Ali, S., & Rather, I. A. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1208044 · Cited by 57

Recent updates on the role of the gut-liver axis in the pathogenesis of NAFLD/NASH, HCC, and beyond

Ohtani, N., Kamiya, T., & Kawada, N. (2023) · Hepatology Communications · doi:10.1097/hc9.0000000000000241 · Cited by 55

Lung and Gut Microbiota as Potential Hidden Driver of Immunotherapy Efficacy in Lung Cancer

Carbone, C., Piro, G., Noia, V. D., D’Argento, E., Vita, E., Ferrara, M. G., Pilotto, S., Milella, M., Cammarota, G., Gasbarrini, A., et al. (2019) · Mediators of Inflammation · doi:10.1155/2019/7652014 · Cited by 54

Lactobacillus salivarius LI01 encapsulated in alginate-pectin microgels ameliorates d-galactosamine-induced acute liver injury in rats

Zhuge, A., Li, B., Yin, Y., Lv, L., Li, Y., Wu, J., Yang, L., Bian, X., Wang, K., Wang, Q., et al. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10749-y · Cited by 54

Dendrobium officinale Polysaccharide Alleviates Intestinal Inflammation by Promoting Small Extracellular Vesicle Packaging of miR-433-3p

Liu, H., Liang, J., Zhong, Y., Xiao, G., Efferth, T., Georgiev, M. I., Vargas-De-La-Cruz, C. B., Bajpai, V. K., Caprioli, G., Liu, J., et al. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c05134 · Cited by 55

Bioactive modulators targeting STING adaptor in cGAS-STING pathway

Feng, X., Liu, D., Li, Z., & Bian, J. (2019) · Drug Discovery Today · doi:10.1016/j.drudis.2019.11.007 · Cited by 53

Bacterial vitamin B12 production enhances nematode predatory behavior

Akduman, N., Lightfoot, J. W., Röseler, W., Witte, H., Lo, W., Rödelsperger, C., & Sommer, R. J. (2020) · The ISME Journal · doi:10.1038/s41396-020-0626-2 · Cited by 53

The effect of bile acids on the growth and global gene expression profiles in Akkermansia muciniphila

Hagi, T., Geerlings, S. Y., Nijsse, B., & Belzer, C. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10976-3 · Cited by 55

Beyond the lesion site: minocycline augments inflammation and anxiety-like behavior following SCI in rats through action on the gut microbiota

Schmidt, E. K. A., Raposo, P. J. F., Espin, A. T., Fenrich, K. K., & Fouad, K. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02123-0 · Cited by 53

The chemistry of gut microbiome in health and diseases

Lau, A., Tan, L. T., Mutalib, N. A., Wong, S. H., Letchumanan, V., & Lee, L. (2021) · Progress In Microbes & Molecular Biology · doi:10.36877/pmmb.a0000175 · Cited by 55

Novel β-mannanase/GLP-1 fusion peptide high effectively ameliorates obesity in a mouse model by modifying balance of gut microbiota

Wang, Y., Ablimit, N., Zhang, Y., Li, J., Wang, X., Liu, J., Miao, T., Wu, L., Wang, H., Wang, Z., et al. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.09.150 · Cited by 53

Reducing bias in microbiome research: Comparing methods from sample collection to sequencing

Kool, J., Tymchenko, L., Shetty, S. A., & Fuentes, S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1094800 · Cited by 54

Eosinophils, probiotics, and the microbiome

Rosenberg, H. F., Masterson, J. C., & Furuta, G. T. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ri0416-202r · Cited by 53

Effects of sulfur-fumigation on the pharmacokinetics, metabolites and analgesic activity of Radix Paeoniae Alba

Kong, M., Liu, H., Wu, J., Shen, M., Wang, Z., Duan, S.-M., Zhang, Y., Zhu, H., & Li, S. (2017) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2017.10.023 · Cited by 52

Autoimmune phenotypes in schizophrenia reveal novel treatment targets

Severance, E. G., Dickerson, F., & Yolken, R. H. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.05.005 · Cited by 52

NLRP6 suppresses the inflammatory response of human periodontal ligament cells by inhibiting NF‐κB and ERK signal pathways

Lu, W. L., Zhang, L., Song, D., Yi, X., Xu, W., Ye, L.-R., & Huang, D. M. (2019) · International Endodontic Journal · doi:10.1111/iej.13091 · Cited by 52

Compartmentalization of Immune Response and Microbial Translocation in Decompensated Cirrhosis

Silva, M. C. A., Schierwagen, R., Pohlmann, A., Magdaleno, F., Uschner, F. E., Ryan, P. B., Vehreschild, M. J. G. T., Clària, J., Latz, E., Lelouvier, B., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00069 · Cited by 52

The lung microbiome in lung transplantation

McGinniss, J. E., Whiteside, S. A., Simón‐Soro, Á., Diamond, J. M., Christie, J. D., Bushman, F. D., & Collman, R. G. (2021) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2021.04.014 · Cited by 53

Can control of gut microbiota be a future therapeutic option for inflammatory bowel disease?

Nishida, A., Nishino, K., Sakai, K., Owaki, Y., Noda, Y., & Imaeda, H. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i23.3317 · Cited by 52

Psychological stress disrupts intestinal epithelial cell function and mucosal integrity through microbe and host-directed processes

Allen, J. M., Mackos, A. R., Jaggers, R. M., Brewster, P. C., Webb, M., Lin, C., Ladaika, C., Davies, R. H., White, P., Loman, B. R., et al. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2035661 · Cited by 53

Link between Viral Infections, Immune System, Inflammation and Diet

Suardi, C., Cazzaniga, E., Graci, S., Dongo, D., & Palestini, P. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18052455 · Cited by 54

Understanding the bidirectional interactions between two-dimensional materials, microorganisms, and the immune system

Peng, G., & Fadeel, B. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114422 · Cited by 54

The gut microbiota and its metabolite butyrate shape metabolism and antiviral immunity along the gut-lung axis in the chicken

Saint-Martin, V., Guillory, V., Chollot, M., Fleurot, I., Kut, E., Roesch, F., Caballero, I., Helloin, E., Chambellon, É., Ferguson, B. J., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06815-0 · Cited by 54

Bats Are an Untapped System for Understanding Microbiome Evolution in Mammals

Ingala, M. R., Simmons, N. B., & Perkins, S. L. (2018) · mSphere · doi:10.1128/msphere.00397-18 · Cited by 51

Microbiome dynamics in obesity

Thaiss, C. A. (2018) · Science · doi:10.1126/science.aav6870 · Cited by 54

Impact of the gut microbiota on immune checkpoint inhibitor-associated toxicities

Pezo, R. C., Wong, M., & Martin, A. (2019) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756284819870911 · Cited by 51

Adjuvant activities of CTAB-modified Polygonatum sibiricum polysaccharide cubosomes on immune responses to ovalbumin in mice

Liu, Z., Ni, H., Yu, L., Xu, S., Bo, R., Qiu, T., Gu, P., Zhu, T., He, J., Wusiman, A., et al. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.01.174 · Cited by 51

The use of fecal microbiota transplant in sepsis

Keskey, R. C., Cone, J., DeFazio, J. R., & Alverdy, J. C. (2020) · Translational research · doi:10.1016/j.trsl.2020.07.002 · Cited by 52

Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women

Mehta, S. D., Nannini, D. R., Otieno, F., Green, S. J., Agingu, W., LANDAY, A. L., Zheng, Y., & Hou, L. (2020) · mSystems · doi:10.1128/msystems.00502-20 · Cited by 53

Typically inhibiting USP14 promotes autophagy in M1-like macrophages and alleviates CLP-induced sepsis

Xu, F., Ma, Y., Huang, W., Gao, J., Guo, M., Li, J., Kong, L., Liang, G., Du, R., Xu, Q., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02898-9 · Cited by 51

Shifts in gut and vaginal microbiomes are associated with cancer recurrence time in women with ovarian cancer

Jacobson, D. K., Moore, K. N., Gunderson, C. C., Rowland, M. R., Austin, R. M., Honap, T. P., Xu, J., Warinner, C., Sankaranarayanan, K., & Lewis, C. M. (2021) · PeerJ · doi:10.7717/peerj.11574 · Cited by 50

Extracellular vesicles hybrid plasmid-loaded lipid nanovesicles for synergistic cancer immunotherapy

Tong, Q., Li, K., Huang, F., Dai, Y., Zhang, T., Muaibati, M., Abasi, A., & Huang, X. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100845 · Cited by 50

Enhanced understanding of the host–pathogen interaction in sepsis: new opportunities for omic approaches

Goh, C., & Knight, J. C. (2017) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30045-0 · Cited by 51

Interplay between Cellular Metabolism and Cytokine Responses during Viral Infection

Zhang, S., Carrière, J., Lin, X., Xie, N., & Feng, P. (2018) · Viruses · doi:10.3390/v10100521 · Cited by 53

The Conceptual Ecology of the Human Microbiome

Morar, N., & Bohannan, B. J. M. (2019) · The Quarterly Review of Biology · doi:10.1086/703582 · Cited by 51

Bone marrow CX3CR1+ mononuclear cells relay a systemic microbiota signal to control hematopoietic progenitors in mice

Lee, S., Kim, H., You, G., Kim, Y., Lee, S., Le, V., Kwon, O., Im, S., Kim, Y., Kim, K. S., et al. (2019) · Blood · doi:10.1182/blood.2019000495 · Cited by 52

Following the community development of SIHUMIx – a new intestinal in vitro model for bioreactor use

Krause, J. L., Schäpe, S. S., Fritz‐Wallace, K., Engelmann, B., Rolle-Kampczyk, U. E., Kleinsteuber, S., Schattenberg, F., Liu, Z., Mueller, S., Jehmlich, N., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2019.1702431 · Cited by 53

Viral strategies predisposing to respiratory bacterial superinfections

Rossi, G. A., Fanous, H., & Colin, A. A. (2020) · Pediatric Pulmonology · doi:10.1002/ppul.24699 · Cited by 54

The involvement of crustaceans toll-like receptors in pathogen recognition

Habib, Y. J., & Zhang, Z. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.04.035 · Cited by 53

Short-term exposure to norfloxacin induces oxidative stress, neurotoxicity and microbiota alteration in juvenile large yellow croaker Pseudosciaena crocea

Wang, X., Hu, M., Gu, H., Zhang, L., Shang, Y., Wang, T., Wang, T., Zeng, J., Ma, L., Huang, W., et al. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.115397 · Cited by 50

Mechanisms of idiosyncratic drug-induced liver injury

Uetrecht, J. (2019) · Advances in pharmacology · doi:10.1016/bs.apha.2018.12.001 · Cited by 49

Microbial regulation of enteroendocrine cells

Arora, T., Vanslette, A. M., Hjorth, S. A., & Bäckhed, F. (2021) · Med · doi:10.1016/j.medj.2021.03.018 · Cited by 52

Recent advances in poor HIV immune reconstitution: what will the future look like?

Zhang, W., & Ruan, L. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1236460 · Cited by 52

Microbiota Composition and the Integration of Exogenous and Endogenous Signals in Reactive Nasal Inflammation

Salzano, F. A., Marino, L., Salzano, G., Botta, R. M., Cascone, G., Fiorenza, U. D., Selleri, C., & Casolaro, V. (2018) · Journal of Immunology Research · doi:10.1155/2018/2724951 · Cited by 49

Ceftriaxone Administration Disrupts Intestinal Homeostasis, Mediating Noninflammatory Proliferation and Dissemination of Commensal Enterococci

Chakraborty, R., Lam, V., Kommineni, S., Stromich, J. J., Hayward, M., Kristich, C. J., & Salzman, N. H. (2018) · Infection and Immunity · doi:10.1128/iai.00674-18 · Cited by 52

Dietary Factors in the Control of Gut Homeostasis, Intestinal Stem Cells, and Colorectal Cancer

Francescangeli, F., Angelis, M. L. D., & Zeuner, A. (2019) · Nutrients · doi:10.3390/nu11122936 · Cited by 51

Detection of Intestinal Dysbiosis in Post-COVID-19 Patients One to Eight Months after Acute Disease Resolution

Ferreira, A. S., Borgonovi, T. F., de Salis, L. V. V., Leite, A. Z., Dantas, A. S., Salis, G. V. V. D., Cruz, G. N. F., de Oliveira, L. F. V., Gomes, E., Penna, A. L. B., et al. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph191610189 · Cited by 49

Protective microbiomes can limit the evolution of host pathogen defense

Metcalf, C. J. E., & Koskella, B. (2019) · Evolution Letters · doi:10.1002/evl3.140 · Cited by 48

Alisma orientalis Beverage Treats Atherosclerosis by Regulating Gut Microbiota in ApoE-/- Mice

Zhu, B., Zhai, Y., Ji, M., Wei, Y., Wu, J., Xue, W., Tao, W. W., & Wu, H. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.570555 · Cited by 48

Biomaterials-Mediated Engineering of the Immune System

Backlund, C. M., Jalili‐Firoozinezhad, S., Kim, B., & Irvine, D. J. (2023) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101721-040259 · Cited by 52

Best practice for wildlife gut microbiome research: A comprehensive review of methodology for 16S rRNA gene investigations

Combrink, L., Humphreys, I. R., Washburn, Q., Arnold, H. K., Stagaman, K., Kasschau, K. D., Jolles, A. E., Beechler, B. R., & Sharpton, T. J. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1092216 · Cited by 54

Cancer cell membrane-coated bacterial ghosts for highly efficient paclitaxel delivery against metastatic lung cancer

Ling, D., Jia, X., Wang, K., Yan, Q., Yuan, B., Du, L., Li, M., & Jin, Y. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.08.012 · Cited by 48

Regulation of Microbiota by Vitamin D Receptor: A Nuclear Weapon in Metabolic Diseases

Bakke, D., Chatterjee, I., Agrawal, A., Dai, Y. D., & Sun, J. (2018) · Nuclear Receptor Research · doi:10.11131/2018/101377 · Cited by 48

The importance of scale in comparative microbiome research: New insights from the gut and glands of captive and wild lemurs

Greene, L. K., Bornbusch, S. L., McKenney, E. A., Harris, R. L., Gorvetzian, S. R., Yoder, A. D., & Drea, C. M. (2019) · American Journal of Primatology · doi:10.1002/ajp.22974 · Cited by 51

Microbiome and metabonomics study of quercetin for the treatment of atherosclerosis

Dong-ning, W., Guan, L. L., Jiang, Y., Ma, S.-H., Sun, Y., Lei, H., Yang, W., & Wang, Q. (2019) · Cardiovascular Diagnosis and Therapy · doi:10.21037/cdt.2019.12.04 · Cited by 48

Increased Colonic Permeability and Lifestyles as Contributing Factors to Obesity and Liver Steatosis

Palo, D. M. D., Garruti, G., Ciaula, A. D., Molina‐Molina, E., Shanmugam, H., Angelis, M. D., & Portincasa, P. (2020) · Nutrients · doi:10.3390/nu12020564 · Cited by 50

Immunological design of commensal communities to treat intestinal infection and inflammation

Brown, R. L., Larkinson, M. L. Y., & Clarke, T. B. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009191 · Cited by 49

Dietary neoagarotetraose extends lifespan and impedes brain aging in mice via regulation of microbiota-gut-brain axis

Li, T., Yang, S., Liu, X., Li, Y., Gu, Z., & Jiang, Z. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.04.014 · Cited by 48

Mechanism of Iron Ion Homeostasis in Intestinal Immunity and Gut Microbiota Remodeling

Bao, H., Wang, Y., Xiong, H., Xia, Y., Cui, Z., & Liu, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020727 · Cited by 48

Microbiota activation and regulation of adaptive immunity

Heidari, M., Vareki, S. M., Yaghobi, R., & Karimi, M. H. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1429436 · Cited by 50

A cross-sectional comparative study of gut bacterial community of Indian and Finnish children

Kumbhare, S. V., Kumar, H., Chowdhury, S. P., Dhotre, D. P., Endo, A., Mättö, J., Ouwehand, A. C., Rautava, S., Joshi, R., Patil, N. P., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-11215-y · Cited by 47

Dectin-1 is essential for IL-1β production through JNK activation and apoptosis in Aspergillus fumigatus keratitis

Yuan, K., Zhao, G., Che, C., Li, C., Lin, J., Zhu, G., & He, K. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.09.008 · Cited by 47

The intestinal microbiota in health and disease: the influence of microbial products on immune cell homeostasis

Abt, M. C., & Artis, D. (2009) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e328331b6b4 · Cited by 111

The Microbes of the Intestine: An Introduction to Their Metabolic and Signaling Capabilities

Hsiao, W., Metz, C. N., Singh, D. P., & Roth, J. (2008) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2008.08.006 · Cited by 84

Deciphering the interdependent labyrinth between gut microbiota and the immune system

Saini, A., Dalal, P., & Sharma, D. (2022) · Letters in Applied Microbiology · doi:10.1111/lam.13775 · Cited by 18

Microbiome and Gut Immunity: Innate Immune Cells

Strowig, T., Thiemann, S., & Diefenbach, A. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_8 · Cited by 9

Bridging intestinal immunity and gut microbiota by metabolites

Wang, G., Huang, S., Wang, Y., Cai, S., Yu, H., Liu, H., Zeng, X., Zhang, G., & Qiao, S. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03190-6 · Cited by 305