Source:http://linkedlifedata.com/resource/pubmed/id/21641399
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2011-6-6
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pubmed:abstractText |
Microbial-induced inflammation is important for eliciting humoral immunity. Genetic defects of NADPH oxidase 2-based proteins interrupt phagocyte superoxide generation and are the basis for the human immunodeficiency chronic granulomatous disease (CGD). Hyperinflammation is also a significant clinical manifestation of CGD. Herein, we evaluated humoral immunity in the phagocyte oxidase p47(phox)-deficient model of CGD and found that UV-inactivated Streptococcus pneumoniae and Listeria monocytogenes (Lm) elicited higher specific antibody (Ab) titers in p47(phox-/-) mice than wild-type (WT) mice. Both organisms elicited robust and distinct antigen-presenting cell maturation phenotypes, including IL-12 hypersecretion, and higher major histocompatibility complex II and costimulatory protein expression in Lm-stimulated p47(phox-/-) dendritic cells (DCs) relative to WT DCs. Furthermore, p47(phox-/-) DCs pulsed with Lm and adoptively transferred into naïve WT mice elicited Ab titers, whereas Lm-pulsed WT DCs did not elicit these titers. The observed robust p47(phox-/-) mouse humoral response was recapitulated with live Lm and sustained in vivo in p47(phox-/-) mice. Notably, anti-serum samples from p47(phox-/-) mice that survived secondary Lm infection were protective in WT and p47(phox-/-) mice that were rechallenged with secondary lethal Lm infection. These findings demonstrate a novel benefit of NADPH oxidase 2 deficiency (ie, dependent inflammation in antigen-presenting cell-mediated humoral immunity) and that anti-Lm Ab can be protective in an immunodeficient CGD host.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1525-2191
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pubmed:author | |
pubmed:copyrightInfo |
Published by Elsevier Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
178
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2774-82
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pubmed:meshHeading |
pubmed-meshheading:21641399-Animals,
pubmed-meshheading:21641399-Antibody Formation,
pubmed-meshheading:21641399-Antigen-Presenting Cells,
pubmed-meshheading:21641399-Cell Differentiation,
pubmed-meshheading:21641399-Cytokines,
pubmed-meshheading:21641399-Dendritic Cells,
pubmed-meshheading:21641399-Humans,
pubmed-meshheading:21641399-Immune Sera,
pubmed-meshheading:21641399-Immunity, Humoral,
pubmed-meshheading:21641399-Listeria monocytogenes,
pubmed-meshheading:21641399-Listeriosis,
pubmed-meshheading:21641399-Mice,
pubmed-meshheading:21641399-Mice, Inbred C57BL,
pubmed-meshheading:21641399-Mice, Knockout,
pubmed-meshheading:21641399-NADPH Oxidase,
pubmed-meshheading:21641399-Spleen,
pubmed-meshheading:21641399-Streptococcus pneumoniae
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pubmed:year |
2011
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pubmed:articleTitle |
Role of p47phox in antigen-presenting cell-mediated regulation of humoral immunity in mice.
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pubmed:affiliation |
Molecular Trafficking Unit, Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural,
Research Support, N.I.H., Intramural
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