Egyszerű nézet

dc.contributor.author Bene, László
dc.contributor.author Füst, György
dc.contributor.author Huszti Z
dc.contributor.author Hernadi Z
dc.contributor.author Fekete, Béla
dc.contributor.author Meszaros M
dc.contributor.author Veres, Amarilla
dc.contributor.author Kovacs A
dc.contributor.author Miklos K
dc.contributor.author Singh M
dc.contributor.author Romics, László
dc.contributor.author Prohászka, Zoltán
dc.date.accessioned 2018-10-08T08:41:46Z
dc.date.available 2018-10-08T08:41:46Z
dc.date.issued 2002
dc.identifier 0036314694
dc.identifier.citation pagination=1432-1437; journalVolume=47; journalIssueNumber=7; journalTitle=DIGESTIVE DISEASES AND SCIENCES;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/6407
dc.identifier.uri doi:10.1023/A:1015882127674
dc.description.abstract Since only scarce data are available on the immune response against heat shock proteins (HSP) in inflammatory bowel disease (IBD), we have measured with an ELISA method serum levels of IgG, IgA, and IgM antibodies to mycobacterial HSP65 and human HSP60 in 66 patients with Crohn's disease (CD), 42 patients with ulcerative colitis (UC), and 126 age- and gender-matched healthy controls. Serum concentration [median (25th-75th percentiles) of IgG anti-HSP65 antibodies was substantially lower in patients with either CD (P < 0.01) or UC (P < 0.001) than in healthy controls, while no difference was found in the levels of anti-HSP60 antibodies. Low anti-HSP65 antibody levels were measured in patients with active CD and in both active and inactive UC, and only in IBD patients with no extraintestinal manifestations. In conclusion, our present findings indicate that an abnormal immune response to bacterial HSP65 or some epitopes of the protein may contribute to the dysregulation of host defenses against certain intestinal bacteria.
dc.relation.ispartof urn:issn:0163-2116
dc.title Impaired humoral immune response against mycobacterial 65-kDa heat shock protein (HSP65) in patients with inflammatory bowel disease
dc.type Journal Article
dc.date.updated 2018-09-02T12:16:08Z
dc.language.rfc3066 en
dc.identifier.mtmt 1070633
dc.identifier.wos 000176184500003
dc.identifier.pubmed 12141797
dc.contributor.department SE/AOK/K/III. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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