Publication
The B-cell inhibitory receptor CD22 is a major factor in host resistance to Streptococcus pneumoniae infection
dc.contributor.author | Fernandes, Vitor E. | |
dc.contributor.author | Ercoli, Giuseppe | |
dc.contributor.author | Bénard, Alan | |
dc.contributor.author | Brandl, Carolin | |
dc.contributor.author | Fahnenstiel, Hannah | |
dc.contributor.author | Müller-Winkler, Jennifer | |
dc.contributor.author | Weber, Georg F. | |
dc.contributor.author | Denny, Paul | |
dc.contributor.author | Nitschke, Lars | |
dc.contributor.author | Andrew, Peter W. | |
dc.date.accessioned | 2020-09-02T08:41:23Z | |
dc.date.available | 2020-09-02T08:41:23Z | |
dc.date.issued | 2020 | |
dc.description.abstract | Streptococcus pneumoniae is a major human pathogen, causing pneumonia and sepsis. Genetic components strongly influence host responses to pneumococcal infections, but the responsible loci are unknown. We have previously identified a locus on mouse chromosome 7 from a susceptible mouse strain, CBA/Ca, to be crucial for pneumococcal infection. Here we identify a responsible gene, Cd22, which carries a point mutation in the CBA/Ca strain, leading to loss of CD22 on B cells. CBA/Ca mice and gene-targeted CD22-deficient mice on a C57BL/6 background are both similarly susceptible to pneumococcal infection, as shown by bacterial replication in the lungs, high bacteremia and early death. After bacterial infections, CD22-deficient mice had strongly reduced B cell populations in the lung, including GM-CSF producing, IgM secreting innate response activator B cells, which are crucial for protection. This study provides striking evidence that CD22 is crucial for protection during invasive pneumococcal disease. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.doi | 10.1371/journal.ppat.1008464 | pt_PT |
dc.identifier.issn | 1553-7366 | |
dc.identifier.uri | http://hdl.handle.net/10400.1/14668 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Public Library of Science | pt_PT |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt_PT |
dc.subject | Animals | pt_PT |
dc.subject | B-Lymphocytes | pt_PT |
dc.subject | Bacteremia | pt_PT |
dc.subject | Female | pt_PT |
dc.subject | Host-Pathogen Interactions | pt_PT |
dc.subject | Humans | pt_PT |
dc.subject | Male | pt_PT |
dc.subject | Mice | pt_PT |
dc.subject | Mice, Inbred BALB C | pt_PT |
dc.subject | Mice, Inbred C57BL | pt_PT |
dc.subject | Mice, Inbred CBA | pt_PT |
dc.subject | Pneumococcal Infections | pt_PT |
dc.subject | Pneumonia, Pneumococcal | pt_PT |
dc.subject | Sialic Acid Binding Ig-like Lectin 2 | pt_PT |
dc.subject | Streptococcus pneumoniae | pt_PT |
dc.title | The B-cell inhibitory receptor CD22 is a major factor in host resistance to Streptococcus pneumoniae infection | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.issue | 4 | pt_PT |
oaire.citation.startPage | e1008464 | pt_PT |
oaire.citation.title | PLoS Pathogens | pt_PT |
oaire.citation.volume | 16 | pt_PT |
person.familyName | Denny | |
person.givenName | Paul | |
person.identifier.orcid | 0000-0003-4659-6893 | |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |
relation.isAuthorOfPublication | b0b3224b-5aeb-4cdb-8ed9-bd83d0017204 | |
relation.isAuthorOfPublication.latestForDiscovery | b0b3224b-5aeb-4cdb-8ed9-bd83d0017204 |
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