The essential role of complement in antibody-mediated resistance to Salmonella.
cam.issuedOnline | 2018-10-10 | |
dc.contributor.author | Rossi, Omar | |
dc.contributor.author | Coward, Chris | |
dc.contributor.author | Goh, Yun Shan | |
dc.contributor.author | Claassens, Jill WC | |
dc.contributor.author | MacLennan, Calman A | |
dc.contributor.author | Verbeek, Sjef J | |
dc.contributor.author | Mastroeni, Pietro | |
dc.contributor.orcid | Mastroeni, Pietro [0000-0003-3838-4962] | |
dc.date.accessioned | 2018-11-14T00:31:31Z | |
dc.date.available | 2018-11-14T00:31:31Z | |
dc.date.issued | 2019-01 | |
dc.description.abstract | Vaccines can serve as essential tools to prevent bacterial diseases via the induction of long-lasting IgG responses. The efficacy of such vaccines depends on the effector mechanisms triggered by IgG. The complement system and Fc-gamma receptors (FcγRs) can potentially play a crucial role in IgG-mediated immunity against bacterial diseases. However, their relative importance in vivo is unclear, and has been the object of controversy and debate. In this brief study, we have used gene-targeted mice lacking either FcγRI, II, II and IV or the C3 complement component as well as a novel mouse strain lacking both C3 and FcγRs to conclusively show the essential role of complement in antibody-mediated host resistance to Salmonella enterica systemic infection. By comparing the effect of IgG2a antibodies against Salmonella O-antigen in gene-targeted mice, we demonstrate that the complement system is essential for the IgG-mediated reduction of bacterial numbers in the tissues. | |
dc.format.medium | Print-Electronic | |
dc.identifier.doi | 10.17863/CAM.32423 | |
dc.identifier.eissn | 1365-2567 | |
dc.identifier.issn | 0019-2805 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/285053 | |
dc.language | eng | |
dc.publisher | Wiley | |
dc.publisher.url | http://dx.doi.org/10.1111/imm.13000 | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Salmonella | |
dc.subject | in vivo | |
dc.subject | C3 | |
dc.subject | FcγR | |
dc.subject | complement | |
dc.subject | infection | |
dc.subject | Animals | |
dc.subject | Bacterial Load | |
dc.subject | Complement Activation | |
dc.subject | Complement C3 | |
dc.subject | Humans | |
dc.subject | Immunity, Humoral | |
dc.subject | Immunoglobulin G | |
dc.subject | Mice | |
dc.subject | Mice, Inbred C57BL | |
dc.subject | Mice, Knockout | |
dc.subject | O Antigens | |
dc.subject | Receptors, IgG | |
dc.subject | Salmonella Infections | |
dc.subject | Salmonella Vaccines | |
dc.subject | Salmonella enterica | |
dc.title | The essential role of complement in antibody-mediated resistance to Salmonella. | |
dc.type | Article | |
dcterms.dateAccepted | 2018-08-20 | |
prism.endingPage | 73 | |
prism.issueIdentifier | 1 | |
prism.publicationDate | 2019 | |
prism.publicationName | Immunology | |
prism.startingPage | 69 | |
prism.volume | 156 | |
pubs.funder-project-id | Biotechnology and Biological Sciences Research Council (BB/M000982/1) | |
pubs.funder-project-id | Medical Research Council (G0001245) | |
rioxxterms.licenseref.startdate | 2019-01 | |
rioxxterms.licenseref.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.type | Journal Article/Review | |
rioxxterms.version | VoR | |
rioxxterms.versionofrecord | 10.1111/imm.13000 |
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