Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-2-17
pubmed:abstractText
Bacterial DNA motifs (such as CpG-oligodeoxynucleotides: CpG-ODN) induce innate immune responses via binding to Toll-like-receptor-9 (TLR-9). In murine intestinal mucosa treatment with CpG-ODN worsens chronic intestinal inflammation, whereas it prevents or ameliorates colitis when given in a prophylactic setting. In tonsils B cells have been reported to express TLR-9, especially after activation. Whether B cells in the human intestinal mucosa also express TLR-9 and whether their function can be influenced by CpG-ODN is, so far, unknown. Mucosal B cells were isolated according to a new protocol from surgical specimens of patients with inflammatory bowel disease and from controls by collagenase digestion followed by magnetic cell sorting using anti-CD19 antibody armed magnetic beads. TLR-9 mRNA and protein expression were quantified by real-time polymerase chain reaction (PCR) and Western blot, respectively. Immunoglobulin A (IgA) secretion was measured by enzyme-linked immunosorbent assay after stimulation of isolated B cells with CpG-ODN, control GpC-ODN or lipopolysaccharide (LPS). Flow cytometric analysis of the isolated lamina propria mononuclear cells showed a purification of 73% (+/-22%) CD19(+) cells. By quantitative reverse transcription-PCR and by Western blot TLR-9 expression in this cell population was evident. IgA secretion was increased significantly by CpG-ODN incubation compared with GpC-ODN and LPS. Compared with unstimulated controls, CpG-ODN up-regulated IgA secretion to 139% (+/-21%). These data demonstrate that CD19(+) mucosal B cells express TLR-9 and secrete increased levels of IgA upon stimulation with CpG-ODN, indicating an additional link between adaptive and innate intestinal immune responses.
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1365-2249
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
155
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
534-40
pubmed:dateRevised
2010-9-23
pubmed:meshHeading
pubmed-meshheading:19220839-Antigens, CD19, pubmed-meshheading:19220839-Antigens, CD4, pubmed-meshheading:19220839-B-Lymphocytes, pubmed-meshheading:19220839-Blotting, Western, pubmed-meshheading:19220839-Cell Separation, pubmed-meshheading:19220839-Cells, Cultured, pubmed-meshheading:19220839-Colon, pubmed-meshheading:19220839-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:19220839-Flow Cytometry, pubmed-meshheading:19220839-Humans, pubmed-meshheading:19220839-Immunity, Innate, pubmed-meshheading:19220839-Immunoglobulin A, pubmed-meshheading:19220839-Intestinal Mucosa, pubmed-meshheading:19220839-Lipopolysaccharides, pubmed-meshheading:19220839-Oligodeoxyribonucleotides, pubmed-meshheading:19220839-RNA, Messenger, pubmed-meshheading:19220839-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:19220839-Stimulation, Chemical, pubmed-meshheading:19220839-Toll-Like Receptor 9
pubmed:year
2009
pubmed:articleTitle
CpG-oligodeoxynucleotides stimulate immunoglobulin A secretion in intestinal mucosal B cells.
pubmed:affiliation
Department of Internal Medicine I, University of Regensburg, Regensburg, Germany. stefan.blaas@klinik.uni-regensburg.de
pubmed:publicationType
Journal Article