Characterization of changes in serum anti-glycan antibodies in Crohn's disease--a longitudinal analysis.
Characterization of changes in serum anti-glycan antibodies in Crohn's disease--a longitudinal analysis.
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DOI:
10.1371/journal.pone.0018172
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发表时间:
2011-05-06
期刊:
影响因子:
3.7
通讯作者:
Klebl F
中科院分区:
文献类型:
--
作者:
Rieder F;Lopez R;Franke A;Wolf A;Schleder S;Dirmeier A;Schirbel A;Rosenstiel P;Dotan N;Schreiber S;Rogler G;Klebl F
Anti-glycan antibodies are a promising tool for differential diagnosis and disease stratification of patients with Crohn's disease (CD). We longitudinally assessed level and status changes of anti-glycan antibodies over time in individual CD patients as well as determinants of this phenomenon. 859 serum samples derived from a cohort of 253 inflammatory bowel disease (IBD) patients (207 CD, 46 ulcerative colitis (UC)) were tested for the presence of anti-laminarin (Anti-L), anti-chitin (Anti-C), anti-chitobioside (ACCA), anti-laminaribioside (ALCA), anti-mannobioside (AMCA) and anti-Saccharomyces cerevisiae (gASCA) antibodies by ELISA. All patients had at least two and up to eleven serum samples taken during the disease course. Median follow-up time for CD was 17.4 months (Interquartile range (IQR) 8.0, 31.6 months) and for UC 10.9 months (IQR 4.9, 21.0 months). In a subgroup of CD subjects marked changes in the overall immune response (quartile sum score) and levels of individual markers were observed over time. The marker status (positive versus negative) remained widely stable. Neither clinical phenotype nor NOD2 genotype was associated with the observed fluctuations. In a longitudinal analysis neither changes in disease activity nor CD behavior led to alterations in the levels of the glycan markers. The ability of the panel to discriminate CD from UC or its association with CD phenotypes remained stable during follow-up. In the serum of UC patients neither significant level nor status changes were observed. While the levels of anti-glycan antibodies fluctuate in a subgroup of CD patients the antibody status is widely stable over time.
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DOI:
10.1016/j.cgh.2008.04.032
发表时间:
2008-10
期刊:
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
影响因子:
--
作者:
Dubinsky MC;Kugathasan S;Mei L;Picornell Y;Nebel J;Wrobel I;Quiros A;Silber G;Wahbeh G;Katzir L;Vasiliauskas E;Bahar R;Otley A;Mack D;Evans J;Rosh J;Hemker MO;Leleiko N;Crandall W;Langton C;Landers C;Taylor KD;Targan SR;Rotter JI;Markowitz J;Hyams J;Western Regional Pediatric IBD Research Alliance;Pediatric IBD Collaborative Research Group;Wisconsin Pediatric IBD Alliance
通讯作者:
Wisconsin Pediatric IBD Alliance
影响因子:
2.6
作者:
Dotan, N.;Altstock, R. T.;Dukler, A.
通讯作者:
Dukler, A.
影响因子:
29.4
作者:
Landers, CJ;Cohavy, O;Targan, SR
通讯作者:
Targan, SR
DOI:
10.1046/j.1440-1746.2000.02357.x
发表时间:
2000-12-01
影响因子:
4.1
作者:
Oshitani, N;Hato, F;Kuroki, T
通讯作者:
Kuroki, T
影响因子:
29.4
作者:
FARMER, RG;WHELAN, G;FAZIO, VW
通讯作者:
FAZIO, VW