The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.
Bacterial flagellins: mediators of pathogenicity and host immune responses in mucosa
Open accessAbstract
Flagella contribute to the virulence of pathogenic bacteria through chemotaxis, adhesion to and invasion of host surfaces. Flagellin is the structural protein that forms the major portion of flagellar filaments. Thus, flagellin consists of a conserved domain that is widespread in bacterial species and is dedicated to filament polymerization. Conversely, mammalian hosts detect the conserved domain on flagellin monomers through Toll-like receptor (TLR) 5, which triggers proinflammatory and adaptive immune responses. This review describes the relationships among flagellin molecular structure, bacterial virulence and host defenses, with special emphasis on mucosal tissues.
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The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5
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Toll Pathway-Dependent Blockade of CD4 + CD25 + T Cell-Mediated Suppression by Dendritic Cells
Pasare, C., & Medzhitov, R. (2003) · Science · doi:10.1126/science.1078231 · Cited by 1,997
Induction of Protective IgA by Intestinal Dendritic Cells Carrying Commensal Bacteria
Macpherson, A. J., & Uhr, T. (2004) · Science · doi:10.1126/science.1091334 · Cited by 1,584
Dendritic-cell control of pathogen-driven T-cell polarization
Kapsenberg, M. L. (2003) · Nature Reviews Immunology · doi:10.1038/nri1246 · Cited by 1,437
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Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells
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How Bacteria Assemble Flagella
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Cited by
Mucin dynamics and enteric pathogens
McGuckin, M. A., Lindén, S. K., Sutton, P., & Florin, T. H. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2538 · Cited by 1,428
Pathogenesis of Proteus mirabilis Infection
Armbruster, C. E., Mobley, H. L. T., & Pearson, M. M. (2018) · EcoSal Plus · doi:10.1128/ecosalplus.esp-0009-2017 · Cited by 409
Bacteria and host interactions in the gut epithelial barrier
Ashida, H., Ogawa, M., Kim, M., Mimuro, H., & Sasakawa, C. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.741 · Cited by 337
Speer, T., Rohrer, L., Blyszczuk, P., Shroff, R., Kuschnerus, K., Kränkel, N., Kania, G., Zewinger, S., Akhmedov, A., Shi, Y., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.02.009 · Cited by 310
Oral microbiome: a review of its impact on oral and systemic health
Rajasekaran, J. J., Krishnamurthy, H. K., Bosco, J., Jayaraman, V., Krishna, K., Wang, T., & Bei, K. (2024) · Microorganisms · doi:10.3390/microorganisms12091797 · Cited by 272
Metadata
- Authors
- Ramos, H. C., Rumbo, M., & Sirard, J.-C.
- Venue
- Trends in Microbiology
- Publisher
- Elsevier BV
- Published
- 2004-11
- Volume
- 12
- Issue
- 11
- Pages
- 509-517
- ISSN
- 0966-842X (ISSN-L)
- OpenAlex
- W2137003603
- Cited by
- 485
- References
- 56
- FWCI
- 1.29
- Type
- journal article
- Language
- en
- Open access
- green
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.