The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Segmented Filamentous Bacteria Are Potent Stimuli of a Physiologically Normal State of the Murine Gut Mucosal Immune System
Open accessAbstract
Segmented filamentous bacteria (SFB) are autochthonous bacteria inhabiting the intestinal tracts of many species, including humans. We studied the effect of SFB on the mucosal immune system by monoassociating formerly germfree C3H/HeN mice with SFB. At various time points during 190 days of colonization, fragment cultures of small intestine and Peyer's patches (PP) were analyzed for total immunoglobulin A (IgA) and SFB-specific IgA production. Also, phenotypic changes indicating germinal center reactions (GCRs) and the activation of CD4(+) T cells in PP were determined by using fluorescence-activated cell sorter analyses. A second group of SFB-monoassociated mice was colonized with a gram-negative commensal, Morganella morganii, to determine if the mucosal immune system was again stimulated and to evaluate the effect of prior colonization with SFB on the ability of M. morganii to translocate to the spleen and mesenteric lymph nodes. We found that SFB stimulated GCRs in PP from day 6 after monoassociation, that GCRs only gradually waned over the entire length of colonization, that natural IgA production was increased to levels 24 to 63% of that of conventionally reared mice, and that SFB-specific IgA was produced but accounted for less than 1.4% of total IgA. Also, the proportion of CD4(+), CD45RBlow T cells, indicative of activated cells, gradually increased in the PP to the level found in conventionally reared mice. Secondary colonization with M. morganii was able to stimulate GCRs anew, leading to a specific IgA antibody response. Previous stimulation of mucosal immunity by SFB did not prevent the translocation of M. morganii in the double-colonized mice. Our findings generally indicate that SFB are one of the single most potent microbial stimuli of the gut mucosal immune system.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“segmented filamentous bacteria are critical promoters of intestinal mucosal IgA production (39, 40)and Th17 cell induction (41, 42)”
From Respiratory viral infection-induced microbiome alterations and secondary bacterial pneumonia. (2018) · cites this paper as [40]
Citations
Cites
Shroff, K. E., Meslin, K., & Cebra, J. J. (1995) · Infection and Immunity · doi:10.1128/iai.63.10.3904-3913.1995 · Cited by 395
Self-citationCong, Y., Brandwein, S. L., McCabe, R. P., Lazenby, A., Birkenmeier, E. H., Sundberg, J. P., & Elson, C. O. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.6.855 · Cited by 383
Umesaki, Y., Okada, Y., Matsumoto, S., Imaoka, A., & Setoyama, H. (1995) · Microbiology and Immunology · doi:10.1111/j.1348-0421.1995.tb02242.x · Cited by 346
Moreau, M.-C., Ducluzeau, R., Guy‐Grand, D., & Muller, M. C. (1978) · Infection and Immunity · doi:10.1128/iai.21.2.532-539.1978 · Cited by 232
Apathogenic, intestinal, segmented, filamentous bacteria stimulate the mucosal immune system of mice
Klaasen, H. L., Van der Heijden, P. J., Stok, W., Poelma, F. G., Koopman, J. P., Van den Brink, M. E., Bakker, M. H., Eling, W. M., & Beynen, A. C. (1993) · Infection and Immunity · doi:10.1128/iai.61.1.303-306.1993 · Cited by 231
Functional and ontogenetic analysis of murine CD45Rhi and CD45Rlo CD4+ T cells.
Lee, W. T., Yin, X. M., & Vitetta, E. S. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.144.9.3288 · Cited by 227
Davis, C. P., & Savage, D. C. (1974) · Infection and Immunity · doi:10.1128/iai.10.4.948-956.1974 · Cited by 206
SNEL, J., Heinen, P. P., Blok, H. J., Carman, R. J., Duncan, A. J., Allen, P. C., & Collins, M. D. (1995) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-45-4-780 · Cited by 179
Long-term CD4+ memory T cells from the spleen lack MEL-14, the lymph node homing receptor
Bradley, L. M., Atkins, G., & Swain, S. L. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.2.324 · Cited by 164
Weinstein, P. D., & Cebra, J. J. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.12.4126 · Cited by 145
Self-citation
Research works printed but not linked: 1
- Leidy J. On the existence of entophyta in healthy animals, as a natural condition.Proc. Natl. Acad. Sci. USA41849225233
Cited by
Sorted by citations
Items 301–400 of 408
Rat salivary gland reveals a more restricted IgA repertoire than ileum
Stoel, M., Evenhuis, W. N. H., Kroese, F. G. M., & Bos, N. A. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.07.001 · Cited by 11
Self-citationIgA Determines Bacterial Composition in the Gut
Gupta, S., Gupta, S. L., Singh, A., Oswal, N., Bal, V., Rath, S., George, A., & Basu, S. (2023) · Crohn s & Colitis 360 · doi:10.1093/crocol/otad030 · Cited by 12
Misic, A. M., Miedel, E. L., Brice, A. K., Cole, S. D., Zhang, G. F., Dyer, C., Secreto, A. J., Smith, A. L., Danet-Desnoyers, G. A., & Beiting, D. P. (2018) · Comparative Medicine · doi:10.30802/aalas-cm-17-000084 · Cited by 10
Sporulation in Bacteria: Beyond the Standard Model
Hutchison, E. A., Miller, D. A., & Angert, E. R. (2016) · ASM Press eBooks · doi:10.1128/9781555819323.ch4 · Cited by 10
Self or non-self? The multifaceted role of the microbiota in immune-mediated diseases
Kriegel, M. A. (2015) · Clinical Immunology · doi:10.1016/j.clim.2015.05.010 · Cited by 10
Relationship between T cells and microbiota in health and disease
Kageyama, T., Matsuo, T., Kurakake, R., & Sano, T. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.03.007 · Cited by 9
Fadlallah, S. M., Bitar, E. R., Hussein, H. M., Jallad, M.-A., Matar, G. M., & Rahal, E. A. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.02042-23 · Cited by 8
Ming, G., Zheng, Y., Tang, S., Fang, Z., Wang, T., Li, K., Chen, H., Zhang, J., Zhou, N., Wei, X., et al. (2026) · Microbiome · doi:10.1186/s40168-026-02370-4 · Cited by 7
Xie, R., Jiang, P., Li, L., Yu, B., Wang, C., Pan, Y., Rao, J., Wei, W., & Qiao, Y. (2020) · The FASEB Journal · doi:10.1096/fj.201902680rr · Cited by 8
Auci, D. L. (2016) · Journal of Gastroenterology Pancreatology & Liver Disorders · doi:10.15226/2374-815x/3/4/00166 · Cited by 7
Shi, H. N., & Walker, W. A. (2004) · Bioscience and Microflora · doi:10.12938/bifidus.23.55 · Cited by 8
Mantis, N. J. (2011) · Mucosal Immunology · doi:10.1038/mi.2011.42 · Cited by 8
α-Glucosidase inhibitors boost gut immunity by inducing IgA responses in Peyer’s patches
Hattori-Muroi, K., Naganawa-Asaoka, H., Kabumoto, Y., Tsukamoto, K., Fujisaki, Y., Fujimura, Y., Komiyama, S., Kinashi, Y., Kato, M., Sato, S., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1277637 · Cited by 7
Pattaroni, C., Macowan, M. G., Chatzis, R., Iacono, G., Cardwell, B., Gore, M. L., Čustović, A., Shields, M. D., Power, U. F., Grigg, J., et al. (2025) · Science Advances · doi:10.1126/sciadv.adw1410 · Cited by 7
Gastrointestinal Mucosal Immunology and Mechanisms of Inflammation
MURCH, S. H. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4377-0774-8.10006-5 · Cited by 7
Nowrouzian, F. L., Svensson‐Stadler, L., Adlerberth, I., & Wold, A. E. (2017) · Apmis · doi:10.1111/apm.12743 · Cited by 7
Review: Postnatal development of the mucosal immune system and consequences on health in adulthood
Lewis, M. C., Inman, C. F., & Bailey, M. (2010) · Canadian Journal of Animal Science · doi:10.4141/cjas09112 · Cited by 7
Gut–Brain Axis: Role of the Gut Microbiome on Human Health
Poojara, L., Acharya, D., Patel, J. K., & Rawal, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-1626-6_8 · Cited by 7
Hedblom, G. A., Dev, K., Bowden, S. D., & Baumler, D. J. (2022) · BMC Genomics · doi:10.1186/s12864-022-08886-x · Cited by 6
Innate Immunity and Inflammation
McKarns, S. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64228-9 · Cited by 6
Food Allergy and the Microbiota: Implications for Probiotic Use in Regulating Allergic Responses
Fu, L., Cherayil, B. J., Shi, H., Wang, Y., & Zhu, Y. (2019) · Springer eBooks · doi:10.1007/978-981-13-6928-5_8 · Cited by 5
Brandtzæg, P., & Johansen, F. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8412-6_3 · Cited by 5
B-1 Cells and the Mucosal Immune System
Bos, N. A., Kroese, F. G. M., & Cebra, J. J. (2005) · Elsevier eBooks · doi:10.1016/b978-012491543-5/50037-1 · Cited by 5
Self-citationImmunotherapeutic potential of “Breg-Treg” vs “Th9-Th17” cell axis in post-menopausal osteoporosis
Bhardwaj, A., Sapra, L., & Srivastava, R. K. (2025) · International Reviews of Immunology · doi:10.1080/08830185.2025.2601515 · Cited by 5
Abanikannda, M. F., Shiflett, M. B., Morais, A. R. C., Hong, J. W., Sealey, W. M., & Bledsoe, J. W. (2024) · Antioxidants · doi:10.3390/antiox13111280 · Cited by 4
Bos, N. A., & Salzman, N. H. (2011) · Immunology Letters · doi:10.1016/j.imlet.2011.02.015 · Cited by 4
Self-citationMucosal B Cell Differentiation and Regulation
Lycke, N. Y., Bemark, M., & Spencer, J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00033-1 · Cited by 4
Microbiota: In Health and in Sickness, From Birth to Death
Kuk, S., Uyar, Y., Karaca, S., & Yazar, S. (2016) · Turkish Journal of Parasitology · doi:10.5152/tpd.2016.4789 · Cited by 4
ALTERATION OF THE GUT MICROBIOME FOR PATIENTS WITH INFLAMMATORY BOWEL DISEASE: A REVIEW
Al-Amrah, H., Saadah, O. I., Mosli, M. H., Edris, S., Al-Hindi, R. R., & Bahieldin, A. (2020) · Applied Ecology and Environmental Research · doi:10.15666/aeer/1805_73797392 · Cited by 3
Oemcke, L. A., Anderson, R. C., Rakonjac, J., McNabb, W. C., & Roy, N. C. (2021) · Access Microbiology · doi:10.1099/acmi.0.000218 · Cited by 4
Restriction of IgA secretion in gut plasma cells is driven by a tissue-specific glycolytic program
Zoccoli-Rodriguez, V., Iwaniec, J., & Wilmore, J. R. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf310 · Cited by 3
Bacteroides fragilis colonization induces protective systemic IgA
Harris, J., Gubitosi, N., Zoccoli-Rodriguez, V., Borg, K. M., Delaney, M., Cruz, T. N., Gaudette, B. T., & Wilmore, J. R. (2025) · Microbiome · doi:10.1186/s40168-025-02222-7 · Cited by 3
Hematopoietic MyD88 orchestrates the control of gut colonization by segmented filamentous bacteria
Cherrier, M., Teo, T., Corrêa, R. O., Picard, M., Couesnon, A., Lebreton, C., Carbone, F., Masson, C., Schnupf, P., Cerf–Bensussan, N., et al. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.03.002 · Cited by 3
Transcription factor c-Rel mediates communication between commensal bacteria and mucosal lymphocytes
Luu, M., Binder, K., Hartmann, S., Kespohl, M., Bazant, J., Romero, R., Schütz, B., Steinhoff, U., & Visekruna, A. (2021) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ab0621-350r · Cited by 3
Dispersal and spatial heterogeneity allow coexistence between enemies and protective mutualists
Poisot, T., Bever, J. D., Thrall, P. H., & Hochberg, M. (2014) · Ecology and Evolution · doi:10.1002/ece3.1151 · Cited by 3
Schoeb, T. R., & Rahija, R. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-409527-4.00026-2 · Cited by 4
Gastrointestinal Mucosal Immunology and Mechanisms of Inflammation
MURCH, S. H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-67293-1.00005-0 · Cited by 3
The human gastrointestinal tract and the significance of intestinal probiotics
Cott, K. I. (2023) · doi:10.52768/jjgastro/1171 · Cited by 2
Song, Y., Wen, S., & Guan, L. L. (2026) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-026-01354-6 · Cited by 2
Hattori-Muroi, K., Maruta, H., Takahashi, D., Kinashi, Y., Hattori, K., Kabumoto, Y., Fujimura, Y., Tsukamoto, S., Suzuki, K., Oguchi, H., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.04.013 · Cited by 4
Gut Microbiota and Their Regulation
Shrestha, A., & Wesemann, D. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397933-9.00017-5 · Cited by 2
Early life host regulation of the mammalian enteric microbiota composition
van Best, N., & Hornef, M. W. (2021) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2021.151498 · Cited by 2
Meleshko, T., Паллаг, О. В., & Boyko, N. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822238-6.00002-9 · Cited by 2
The Regulation of IgA Production
Fagarasan, S., & Macpherson, A. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00023-9 · Cited by 2
Debré, P. (2017) · Biologie Aujourd hui · doi:10.1051/jbio/2017012 · Cited by 2
Cerf–Bensussan, N. (2019) · Cellular Microbiology · doi:10.1111/cmi.13097 · Cited by 2
Beware of whom you live with: Your intestinal IgA may depend on it
Eberl, G., & Vieira, P. (2020) · European Journal of Immunology · doi:10.1002/eji.202048615 · Cited by 2
The role of mucus in the cross talk between gut bacteria and the host
Kober, O. I. (2013) · UEA Digital Repository (University of East Anglia) · Cited by 2
The gut microbiota of Labrador retriever puppies: a longitudinal cohort study
Woolley, C. S. C., Muwonge, A., Bronsvoort, M., Schoenebeck, J. J., Handel, I. G., Chamberlain, K., Rose, E., & Clements, D. N. (2025) · Animal Microbiome · doi:10.1186/s42523-025-00464-2 · Cited by 2
Striking a balance: how the gut microbiome shapes the fate of intestinal CD4+ T cells
Till, J. M., Brock, O. D., & Ahern, P. P. (2025) · Discovery Immunology · doi:10.1093/discim/kyaf020 · Cited by 1
The Role of Bacterial and Parasitic Infections in Chronic Inflammatory Disorders and Autoimmunity
Ehlers, S., & Rook, G. A. W. (2014) · ASM Press eBooks · doi:10.1128/9781555816872.ch41 · Cited by 1
Host Interactions with Bacteria: From “Entente Cordiale” to “Casus Belli”
Lhocine, N., & Sansonetti, P. J. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8256-7_14 · Cited by 1
McCarthy, Ú., Pettinello, R., Feehan, L., Ho, Y., & White, P. (2016) · Diseases of Aquatic Organisms · doi:10.3354/dao02977 · Cited by 1
Debnath, N., Yadav, A. K., & Kumar, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91313-3.00004-0 · Cited by 1
Role of microbiota-gut-brain axis in autoimmunity and multiple sclerosis
Mishra, Y., Maity, D., & Kaundal, R. K. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-21680-0.00007-9 · Cited by 1
Guo, C. (2013) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2vw2m · Cited by 1
Liu, W.-R., Shu, X., Gu, W., Peng, K., Zhao, H., Chen, B., Jiang, L., & Jiang, M. (2019) · PubMed Central · doi:10.7499/j.issn.1008-8830.2019.06.007 · Cited by 1
Risk factors for papillary thyroid cancer in obesity and diabetes mellitus
Gychka, S. G., Serbin, B. Y., Nikolaenk, S. I., Matviian, M. A., Sujima, S., & Товкай, О. А. (2020) · Clinical endocrinology and endocrine surgery · doi:10.30978/cees-2020-3-85 · Cited by 1
Kuraganti, G., Sujatha, E., & Bramhachari, P. V. (2021) · Springer eBooks · doi:10.1007/978-981-16-3156-6_8 · Cited by 1
Abanikannda, M. F., Shiflett, M. B., Morais, A. R. C., Hong, J., Sealey, W. M., & Bledsoe, J. W. (2024) · Preprints.org · doi:10.20944/preprints202408.2069.v1 · Cited by 1
Dias, A. M. M. (2018) · theses.fr (ABES) · doi:10.70675/d23527b7z823fz490fzafeez21e0de6d2406 · Cited by 1
Intestinal Bacteria: Mucosal Tissue Development and Gut Homeostasis
Lanning, D. K., Severson, K. M., & Knight, K. L. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8412-6_5
Bacterial-host interactions in inflammatory bowel disease
von Hegedus, J. H. (2014) · Utrecht University Repository (Utrecht University)
Disturbances in microbiota — cause or effect?
Florin, T. H. (2007) · Springer eBooks · doi:10.1007/978-1-4020-5702-1_10
How to evaluate a gastric submucosal tumour in a patient with haematemesis?
Boujaoudé, J. (2005) · Gut · doi:10.1136/gut.2004.054874
Shaping of mucosal dendritic cells by the intestinal environment
Massacand, J. C. (2009) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-006023200
Utvecklingen av bakteriefloran i magtarmkanalen hos kalvar
Augustsson, J. (2016) · Epsilon Archive for Student Projects (University of Southampton)
Immunomodulating Lactobacilli in Chicken
Koenen, M. E. (2004) · RePub (Erasmus University Rotterdam)
Mucosal homeostasis and inflammatory bowel disease
Reikvam, D. H. (2011) · NORA - Norwegian Open Research Archives
The Role of the Gut Microbiome in Modulating the Pathogenesis of Kawasaki Disease
Chan, K. D. (2014) · TSpace (University of Toronto)
A specific component of the intestinal microbiota exacerbates the severity of allergic asthma
Burgess, S. L. (2013) · OhioLink ETD Center (Ohio Library and Information Network)
Fuentes, S., Egert, M., Jiménez‐Valera, M., Monteoliva‐Sánchez, M., Ruiz‐Bravo, A., & Smidt, H. (2007)
Nociceptor Regulation of the Intestinal Immune Landscape During Salmonella Typhimurium Infection
Potts, D. E. (2019) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Role of microbial metabolites in regulating host immunity
Tadepally, H. D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-821406-0.00004-7
Characterization and Isolation of Segmented Filamentous Bacteria from Commercial Turkey
Hedblom, G. A. (2020) · University of Minnesota Digital Conservancy (University of Minnesota)
Gut microbiota and the immune system and inflammation
Duttaroy, A. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822405-2.00031-1
Zhang, C. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/85829
Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age
Renkema, K. R. (2013) · UA Campus Repository (The University of Arizona)
Savidge, T. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1165605.628651
Ray, A., & Krishnamoorthy, N. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1165605.1505055
Gut Microbiome and Immune Responses in Gastrointestinal Cancer
Laube, R., & Liu, K. (2023) · Springer eBooks · doi:10.1007/978-981-19-4492-5_11 · Cited by 1
Nakanishi, Y., Nozu, R., Ueno, M., Hioki, K., Ishii, C., Murakami, S., Suzuki, K. M., Ka, Y., Ogura, T., Ito, A., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3464296/v1
Gut commensals require Peyer’s patches to induce protective systemic IgA responsesPreprint
Wilmore, J. R., Harris, J., Zoccoli-Rodriguez, V., Delaney, M., Cruz, T., & Guadette, B. (2024) · Research Square · doi:10.21203/rs.3.rs-4220532/v1
Zhang, S., Zhou, R., Xiong, S., Xie, X., Li, L., & Li, Y. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4861698
Microbial hoolIgAn dismantles gut defenses
Slack, E. M. C. (2024) · Science · doi:10.1126/science.ads2152
Ramanathan, J. (2024) · Springer eBooks · doi:10.1007/978-3-031-70088-0_15
NOVEL PERSPECTIVES ON THE CONTRIBUTORS TO INFLAMMATORY BOWEL DISEASE DEVELOPMENT
Kiani, F. A., FAROOQ, A., Javid, M., SALEEM, M., Ahmed, Z., RASOOL, F., KHAN, S., NAWAZ, M., AZEEM, M., & MEHMOOD, K. (2024) · Biological and Clinical Sciences Research Journal · doi:10.54112/bcsrj.v2024i1.1362
Gastrointestinal Mucosal Immunology and Mechanisms of Inflammation
MURCH, S. H., & Edwards, L. A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-11760-2.00005-7
Hattori-Muroi, K., Maruta, H., Takahashi, D., Kinashi, Y., Hattori, K., Kabumoto, Y., Fujimura, Y., Tsukamoto, S., Suzuki, K., Oguchi, H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.12.669459
Innate Immunity and Inflammation
McKarns, S. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.50005-9
Discovery of Novel Probiotic Species to Improve Infant HealthPreprint
Lu, R., Lee, N., Drake, A. J., Fulton, R. P., Abutaleb, N. S., Seleem, M. N., Oakland, D. N., Garin-Laflam, M. P., Pop, M., & Luo, X. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.27.684727
Lécuyer, E. (2012) · OpenGrey (Institut de l'Information Scientifique et Technique)
Hedblom, G. A., Dev, K., Bowden, S. D., & Baumler, D. J. (2022) · Figshare · doi:10.6084/m9.figshare.21152912
Hedblom, G. A., Dev, K., Bowden, S. D., & Baumler, D. J. (2022) · Figshare · doi:10.6084/m9.figshare.21152921
Hedblom, G. A., Dev, K., Bowden, S. D., & Baumler, D. J. (2022) · Figshare · doi:10.6084/m9.figshare.21152915
Hedblom, G. A., Dev, K., Bowden, S. D., & Baumler, D. J. (2022) · Figshare · doi:10.6084/m9.figshare.21152918
Jochum, J., Satheesh, V., Masonbrink, R. E., Rodriguez-Gallegos, J., Wright, D. A., Severin, A. J., & Mellata, M. (2026) · Microorganisms · doi:10.3390/microorganisms14020341
Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal
Soualhi, S. (2014) · theses.fr (ABES) · doi:10.70675/e3d7e0c0z8f92z49e6z8bddz19969fbc94f0
Metadata
- Authors
- Talham, G. L., Jiang, H.-Q., Bos, N. A., & Cebra, J. J.
- Affiliations
- University of Pennsylvania (US)
- University of Groningen (NL)
- ORCID
- Bos, Nicolaas A.
- Venue
- Infection and Immunity
- Publisher
- American Society for Microbiology
- Published
- 1999-04
- Volume
- 67
- Issue
- 4
- Pages
- 1992-2000
- ISSN
- 0019-9567 (ISSN-L)
- 1098-5522
- PMC
- PMC96557
- OpenAlex
- W2106689062
- Cited by
- 408
- References
- 23
- Citations by year
- 2026: 8 · 2025: 16 · 2024: 14 · 2023: 16 · 2022: 15 · 2021: 22 · 2020: 21 · 2019: 13 · 2018: 17 · 2017: 12 · 2016: 24 · 2015: 22 · 2014: 30 · 2013: 29 · 2012: 25
- FWCI
- 1.72
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Infection and Immunity (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Funders
- National Institutes of Health (5r01ai035936-04)
- National Institute of Allergy and Infectious Diseases (AI37108, R37AI037108, R01AI037108, AI-35936)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- segmented filamentous bacteria, gut mucosal immunity, immunoglobulin A, Peyer's patches, germinal center reaction, CD4+ T cell activation, Morganella morganii, commensal bacteria, bacterial translocation, germ-free mice, secondary colonization, small intestine
- MeSH terms
- Animals, Clostridium, Enterobacteriaceae, Female, Intestinal Mucosa, Lymph Nodes, Mesentery, Mice, Inbred BALB C, Mice, Inbred C3H, Spleen, Germinal Center, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review