期刊论文详细信息
European Journal of Medical Research
Increased levels of anti-glycan antibodies in patients with cystic fibrosis
O Schröder3  F Behrens3  TO Wagner3  J Hausmann3  H Hirche2  J Stein1  TO Hirche4 
[1] Department of Gastroenterology, Elisabethen Hospital, Frankfurt, Germany;Institute for Medical Informatics, Biometry and Epidemiology, University of Duisburg-Essen, Essen, Germany;Department of Internal Medicine, Johann Wolfgang Goethe-University Hospital, Frankfurt, Germany;Department of Pulmonary Medicine, German Clinic for Diagnostics (DKD), Wiesbaden, Germany
关键词: ASCA;    anti-glycan antibodies;    crohn's disease;    cystic fibrosis;   
Others  :  824873
DOI  :  10.1186/2047-783X-16-9-385
 received in 2010-12-20, accepted in 2011-05-24,  发布年份 2011
PDF
【 摘 要 】

Background

The prevalence of Crohn's disease (CD) is increased in patients with cystic fibrosis (CF). Anti-Saccharomyces cerevisiae antibodies (ASCA) have been suggested as a screening tool to detect CD in CF. Recently, several new anti-glycan antibodies have been reported in CD.

Materials and methods

The sera of 119 CF patients of various age groups were prospectively screened for ASCA type IgG (gASCA), anti-laminaribioside carbohydrate IgG antibodies (ALCA), anti-chitobioside carbohydrate IgA antibodies (ACCA), and anti-mannobioside carbohydrate IgG antibodies (AMCA). The frequency of these anti-glycan antibodies was then compared in patients with CD, ulcerative colitis, rheumatoid arthritis and healthy volunteers.

Results

A significant number of CF patients were positive for gASCA (51.3% [41.6-60.6]) and up to three other anti-glycan antibodies concurrently. Serum levels of anti-glycan antibodies in CF and CD were not related to parameters of inflammation. Despite the well-documented difference in clinical course between male and female CF patients no gender difference of anti-glycan antibodies was found. In contrast, there was a significant positive correlation between anti-glycan markers and age in CF patients.

Conclusions

Our findings demonstrate for the first time the increased frequency of a panel of anti-glycan antibodies in CF and provide a link between the presence of these serological biomarkers and patient's age. Anti-glycan antibody profiling may therefore become a valuable tool in the care of patients with CF.

【 授权许可】

   
2011 I. Holzapfel Publishers

【 预 览 】
附件列表
Files Size Format View
20140713050737780.pdf 2419KB PDF download
Figure 5. 53KB Image download
Figure 4. 41KB Image download
Figure 3. 39KB Image download
Figure 2. 78KB Image download
Figure 1. 31KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

【 参考文献 】
  • [1]Farrell PM: Improving the health of patients with cystic fibrosis through newborn screening. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. Adv Pediatr 2000, 47:79-115.
  • [2]Strong TV, Boehm K, Collins FS: Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization. J Clin Invest 1994, 93:347-354.
  • [3]Eggermont E: Gastrointestinal manifestations in cystic fibrosis. Eur J Gastroenterol Hepatol 1996, 8:731-738.
  • [4]Wilschanski M: Patterns of gastrointestinal disease associated with mutations of CFTR. Curr Gastroenterol Rep 2008, 10:316-323.
  • [5]Abraham C, Cho JH: Inflammatory bowel disease. N Engl J Med 2009, 361:2066-2078.
  • [6]Lloyd-Still JD: Crohn's disease and cystic fibrosis. Dig Dis Sci 1994, 39:880-885.
  • [7]Peeters M, Joossens S, Vermeire S, Vlietinck R, Bossuyt X, Rutgeerts P: Diagnostic value of anti-Saccharomyces cerevisiae and antineutrophil cytoplasmic autoantibodies in inflammatory bowel disease. Am J Gastroenterol 2001, 96:730-734.
  • [8]Zholudev A, Zurakowski D, Young W, Leichtner A, Bousvaros A: Serologic testing with ANCA, ASCA, and anti-OmpC in children and young adults with Crohn's disease and ulcerative colitis: diagnostic value and correlation with disease phenotype. Am J Gastroenterol 2004, 99:2235-2241.
  • [9]Feizi T: Carbohydrate-mediated recognition systems in innate immunity. Immunol Rev 2000, 173:79-88.
  • [10]Dotan I, Fishman S, Dgani Y, Schwartz M, Karban A, Lerner A, et al.: Antibodies against laminaribioside and chitobioside are novel serologic markers in crohn's disease. Gastroenterology 2006, 131:366-378.
  • [11]Ferrante M, Henckaerts L, Joossens M, Pierik M, Joossens S, Dotan N, et al.: New serological markers in inflammatory bowel disease are associated with complicated disease behaviour. Gut 2007, 56:1394-1403.
  • [12]Simondi D, Mengozzi G, Betteto S, Bonardi R, Ghignone RP, Fagoonee S, et al.: Antiglycan antibodies as serological markers in the differential diagnosis of inflammatory bowel disease. Inflamm Bowel Dis 2008, 14:645-651.
  • [13]Condino AA, Hoffenberg EJ, Accurso F, Penvari C, Anthony M, Gralla J, et al.: Frequency of ASCA seropositivity in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 2005, 41:23-26.
  • [14]Rosenfeld M, Davis R, FitzSimmons S, Pepe M, Ramsey B: Gender gap in cystic fibrosis mortality. Am J Epidemiol 1997, 145:794-803.
  • [15]Papp M, Altorjay I, Dotan N, Palatka K, Foldi I, Tumpek J, et al.: New serological markers for inflammatory bowel disease are associated with earlier age at onset, complicated disease behavior, risk for surgery, and NOD2/CARD15 genotype in a Hungarian IBD cohort. Am J Gastroenterol 2008, 103:665-681.
  • [16]Henckaerts L, Pierik M, Joossens M, Ferrante M, Rutgeerts P, Vermeire S: Mutations in pattern recognition receptor genes modulate seroreactivity to microbial antigens in patients with inflammatory bowel disease. Gut 2007, 56:1536-1542.
  • [17]Lachenal F, Nkana K, Nove-Josserand R, Fabien N, Durieu I: Prevalence and clinical significance of auto-antibodies in adults with cystic fibrosis. Eur Respir J 2009, 34:1079-1085.
  • [18]Vasiliauskas EA, Plevy SE, Landers CJ, Binder SW, Ferguson DM, Yang H, et al.: Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup. Gastroenterology 1996, 110:1810-1819.
  • [19]Harrer M, Reinisch W, Dejaco C, Kratzer V, Gmeiner M, Miehsler W, et al.: Do high serum levels of anti-Saccharomyces cerevisiae antibodies result from a leakiness of the gut barrier in Crohn's disease? Eur J Gastroenterol Hepatol 2003, 15:1281-1285.
  • [20]Vermeire S, Peeters M, Vlietinck R, Joossens S, Den Hond E, Bulteel V, et al.: Anti-Saccharomyces cerevisiae antibodies (ASCA), phenotypes of IBD, and intestinal permeability: a study in IBD families. Inflamm Bowel Dis 2001, 7:8-15.
  • [21]Israeli E, Grotto I, Gilburd B, Balicer RD, Goldin E, Wiik A, et al.: Anti-Saccharomyces cerevisiae and antineutrophil cytoplasmic antibodies as predictors of inflammatory bowel disease. Gut 2005, 54:1232-1236.
  • [22]Lindberg E, Magnusson KE, Tysk C, Järnerot G: Antibody (IgG, IgA, and IgM) to baker's yeast (Saccharomyces cerevisiae), yeast mannan, gliadin, ovalbumin and betalactoglobulin in monozygotic twins with inflammatory bowef disease. Gut 1992, 33:909-913.
  • [23]Konrad A, Rütten C, Flogerzi B, Styner M, Göke B, Seibold F: Immune sensitization to yeast antigens in ASCA positive patients with Crohn's disease. Inflamm Bowel Dis 2004, 10:97-105.
  • [24]Seibold F, Slametschka D, Gregor M, Weber P: Neutrophil autoantibodies: a genetic marker in primary sclerosing cholangitis and ulcerative colitis. Gastroenterology 1994, 107:532-536.
  • [25]Sutton CL, Yang H, Li Z, Rotter JI, Targan SR, Braun J: Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with crohn's disease. Gut 2000, 46:58-63.
  • [26]Leclercq-Foucart J, Forget PP, Van Cutsem JL: Lactulose-rhamnose intestinal permeability in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 1987, 6:66-70.
  • [27]Hsieh MC, Berry HK: Protease inhibitor and defective proteolysis in cystic fibrosis. Dig Dis Sci 1988, 33:282-288.
  • [28]Slomiany A, Liau YH, Carter SR, Newman LJ, Slomiany BL: Mucus glycoprotein fatty acyltransferase in patients with cystic fibrosis: effect on the glycoprotein viscosity. Biochem Biophys Res Commun 1985, 132:299-306.
  • [29]Clarke LL, Gawenis LR, Bradford EM, Judd LM, Boyle KT, Simpson JE, et al.: Abnormal Paneth cell granule dissolution and compromised resistance to bacterial colonization in the intestine of CF mice. Am J Physiol Gastrointest Liver Physiol 2004, 286:G1050-1058.
  • [30]Wehkamp J, Harder J, Weichenthal M, Schwab M, Schäffeler E, Schlee M, et al.: NOD2 (CARD15) mutations in crohn's disease are associated with diminished mucosal alpha-defensin expression. Gut 2004, 53:1658-1664.
  文献评价指标  
  下载次数:64次 浏览次数:48次