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Chronic inflammatory bowel diseases

Clinical information

The most important chronic inflammatory bowel diseases (CIBD) include ulcerative colitis (UC) and Crohn’s disease (CD).

Ulcerative colitis (UC) belongs to the CIBD with autoimmune reactions against the mucosa and submucosa of the colon or rectum and increased immune reactions against the intestinal flora. It is assumed that there is a genetic susceptibility to UC and that it may also be caused by certain environmental factors. The inflammation spreads continuously from the rectum, i.e. from anal to oral.

CD is classified as an autoimmune disease of the intestinal mucosa and is among the CIBD with a high recurrence rate. The chronic granulomatous inflammation, which can affect the whole digestive tract from the oral cavity to the anus, is found in most cases only in the lower small intestine (terminal ileum) and the large intestine (colon), very rarely in the oesophagus and mouth. A discontinuous, segmental attack on the intestinal mucosa, which may affect several separate sections of the intestine simultaneously, is characteristic for CD.

Diagnostics

Initial differentiation between irritable bowel syndrome (IBS) and CIBD is possible by non-invasive antigen detection of calprotectin in stool, which thus allows a crucial precharacterisation of intestine-associated inflammations (see chapter “Calprotectin”). The high diagnostic requirements of a differentiated CIBD determination are met by IIF single assays as well as by various highly specific mosaics (CIBD profiles), which have been developed especially for serological diagnostics of CD and UC.

Autoantibodies against the exocrine pancreas are a reliable marker for CD. They have a high disease-specific significance due to their organ specificity, disease association and frequently high serum concentration. Since the inflammation of the intestinal wall in CD is caused by the autoantigens contained in the pancreas secretion, particularly the proteoglycans CUZD1 and GP2, the determination of autoantibodies against the pancreas antigens rPAg1 (CUZD1) and/or PAg2 (GP2) using IFA represents a new dimension in serological CD diagnostics. Anti-Saccharomyces cerevisiae antibodies (ASCA) are another specific parameter that supports serological CD diagnostics.

Autoantibodies against intestinal goblet cells, which occur exclusively in UC, are pathognomonic markers for this autoimmune disease. The target antigen responsible for UC has not yet been exactly identified. The serological determination of autoantibodies against DNA-bound lactoferrin contributes significantly to the diagnosis of CIBD, particularly of UC.

Methods
Technology Parameter Substrate Species Calibration Ig Class Format Order No.
EUROLINE EUROLINE Autoimmune Gastrointestinal Diseases (IgA)
(tissue transglutaminase (endomysium), gliadin-analogue
fusion peptide (GAF-3X), mannan (ASCA))
EUROLINE IgA
IgA
IgA
05 x 10
16 x 01
64 x 01
DL 1360-0510 A
DL 1360-1601 A
DL 1360-6401 A
EUROLINE EUROLINE Autoimmune Gastrointestinal Diseases (IgG)
(tissue transglutaminase (endomysium),
gliadin-analogue fusion peptide (GAF-3X),
parietal cell antigen (PCA) separately
Intrinsic factor, mannan (ASCA))
EUROLINE IgG
IgG
IgG
16 x 01
50 x 01
64 x 01
DL 1360-1601 G
DL 1360-5001 G
DL 1360-6401 G
IIFT antibodies against pancreas acini
(CUZD1 control; associated with Crohn's disease)
IgG 05 x 02
CA 1391-0502
IIFT CIBD Screen 3
pancreas ag rPAg1(CUZD1) / rPAg2(GP2)
intestinal goblet cells
3 BIOCHIPs per field:
transfected cells
goblet cells
control transfection

EU 90
EU 80
EU 90
IgA/G 10 x 05
10 x 05
FA 1391-1005-3
FB 1391-1005-3
IIFT CIBD Profile 7
upper row:
pancreas ag rPAg1(CUZD1) / rPAg2(GP2)
intestinal goblet cells
pANCA

bottom row:
Saccharomyces cerevisiae


transfected cells
goblet cells
granulocytes (EOH)
control transfection

fungal smear


EU 90
EU 80
human
EU 90

S. cerevisiae
IgA/G 10 x 05
10 x 05
FA 1391-1005-7
FB 1391-1005-7
ChLIA IDS Calprotectin
Sample type: Stool
Antibody-coated magnetic particles Calprotectin quantitative
100 x 01
IS-AI260001
ChLIA IDS Calprotectin Calibrator Set 2 x 0.5 ml calibrator 1/2/3/4/5 Calprotectin 5 concentration levels
IS-AI260201
ChLIA IDS Calprotectin Control Set 3 x 0.5 ml control 1/2 Calprotectin 2 concentration levels
IS-AI260301
ELISA calprotectin
determination in stool
Antibody-coated
microplate wells
0/15/60/240/960/2100 µg/g 96 x 01
EQ 6831-9601 W
ChLIA Faecal Calprotectin ChLIA
Sample type: Stool
Antibody-coated magnetic particles quantitative
01 x 00
LQ 6831-0100 W
ChLIA Control set Faecal Calprotectin ChLIA 2 x 0.5 ml control 1/2 02 x 02
LR 6831-0160 W
NUL IDS Calprotectin Extraction Device
Use in combination with IS-AI26000
Use in combination with IS-AI26000 01 x 01
IS-AI260401
NUL Stool Dosage Tubes, unfilled
Use in combination with EQ / LQ 6831 W
Use in combination with EQ / LQ 6831 W 100 x 01
ZE 6010-0100-3
NUL Stool Dosage Tubes, ready for use
Use in combination with EQ / LQ 6831 W
Use in combination with EQ / LQ 6831 W 45 x 01
ZE 6010-4501-2
ELISA Anti-Saccharomyces cerevisiae ELISA (IgA) antigen-coated
microplate wells
mannan of
S. cerevisiae
2/20/200 RU/ml IgA 96 x 01
EV 2841-9601 A
ELISA Anti-Saccharomyces cerevisiae ELISA (IgG) antigen-coated
microplate wells
mannan of
S. cerevisiae
2/20/200 RU/ml IgG 96 x 01
EV 2841-9601 G
IIFT antibodies against Saccharomyces cerevisiae
IgA positive control
fungal
smear
Saccharomyces
cerevisiae
IgA 05 x 02
CV 2841-0502 A
IIFT antibodies against Saccharomyces cerevisiae
IgG positive control
fungal
smear
Saccharomyces
cerevisiae
IgG 05 x 02
CV 2841-0502 G
IIFT Saccharomyces cerevisiae
negative control
IgA, IgG, IgM 05 x 02
CV 2841-0502 Z
IIFT Saccharomyces cerevisiae fungal
smear
Saccharomyces
cerevisiae
IgA
IgG
IgA
IgG
IgA
IgG
10 x 05
10 x 10
20 x 05
10 x 05
10 x 05
10 x 10
10 x 10
20 x 05
20 x 05
FX 2841-1005
FX 2841-1010
FX 2841-2005
FV 2841-1005 A
FV 2841-1005 G
FV 2841-1010 A
FV 2841-1010 G
FV 2841-2005 A
FV 2841-2005 G
* For research use only, not for in vitro diagnostic use in the sense of EU directive 98/79/EC.
1 Product manufactured by third party. Please contact your local Euroimmun representative for more information.