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![Page 1: Dimitrios P. Bogdanos Professor of Immunopathology The Sheila Sherlock Medalist Autoimmunity in Inflammatory Bowel Diseases.](https://reader033.fdocuments.us/reader033/viewer/2022051516/56649d0b5503460f949de04c/html5/thumbnails/1.jpg)
Dimitrios P. Bogdanos
Professor of Immunopathology The Sheila Sherlock Medalist
Autoimmunity in Inflammatory Bowel DiseasesAutoimmunity in Inflammatory Bowel Diseases
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2008-2013 I have received in the past Lecture Honoraria, Consultation Fees, Expert
Panel Fees, Accommodation/Travel Expenses Coverage
INOVA, EUROIMMUN, Generic Assays, FALK, BIORAD, (King’s College Hospital Charitable Trust)
Part of travel/accommodation expenses are covered by the Organizers
I do not have shares or any other relevant financial or other relationship with a commercial organization that could influence the content of my
presentation
ALL FEES OR HONORIA SUPPORT MY FELLOWS’S RESEARCH INITIATIVES/CONFERENCE TRAVEL EXPENSES
Disclosure statementDisclosure statement
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EUROPEAIDBioradCyBioDiarectEucloneEUROIMMUNGeneric Assays InnoVisionInvitrogen-MabTechMardxMeridian LSMenariniMiltenyiMolecular Probes PeproTechPharmaciaRoche
I have received diagnostic reagents free of charge and/or participated in collaborative projects
AMERICAGileadINOVAIMCCOVirusys
JAPANMBL
Dis
clos
ure
stat
emen
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Dis
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1. Inflammatory Bowel Diseases (IBD)2. Immunology of IBD3. Autoimmunity in IBD
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IBD: IBD: EPIDEMIOLOGY & STATASTICSEPIDEMIOLOGY & STATASTICSEstimated prevalence – Active cases 100/100,000 of general population
Estimated approx 1 million cases in US split equally among CD and UC
More Prevalent in developed/ developing countries
Equal distribution among Male:Female
etiopathogenesis not resolved yet
autoimmunity may play a role
subsets
Crohn’s disease
Ulcerative colitis
Colitis indeterminate
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Ulcerative ColitisUlcerative ColitisAutoimmune Process ?????????????????
Inflammation confined to colon
Bimodal Incidence (Ages 15-40 yrs OR 50-80 yrs)
Signs and symptoms: Rectal bleeding, loose bloody stools, passage of mucus from rectum, abdominal pain
Complications: perforation, stricture, megacolon, cancer
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Ulcerative ColitisUlcerative Colitis
Inflammation confined to Treatment: Medical:
Mild/moderate disease—5-ASA, corticosteroids Severe disease—IV steroids or immunosuppressants for refractory disease
Surgical: Proctocolectomy (curative)
Indications: Failure of medical therapy, increasing risk of cancer with long standing disease, bleeding, perforation
Prognosis: Approximately 1-2% risk of cancer at 10 years, 1%/year thereafter
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Imaging Imaging Ulcerative ColitisUlcerative Colitis• Barium Enema vs.
CT– Barium Enema is no
longer the test of choice
• Findings– Continuous lesions
from rectum proximally with circumferential involvement
Lead Pipe SignLead Pipe Sign Repeated episodes of mucosal ulceration and marked muscularis Repeated episodes of mucosal ulceration and marked muscularis
hypertrophy results in shortening, narrowing and smoothing out of the hypertrophy results in shortening, narrowing and smoothing out of the normal haustral markings. normal haustral markings.
““Lead pipe” appearance of colon due to chronic scarring and Lead pipe” appearance of colon due to chronic scarring and retraction/loss of haustraretraction/loss of haustra
Weinstein A et al. A super ‘lead pipe’ colon: radio-pathological correlation of long-standing ulcerative colitis. SA Journal of Radiology;2008 Oct:70-72
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Imaging Crohn’s DiseaseImaging Crohn’s Disease• Small bowel contrast study vs CT
– SBFT useful for characterizing length of involvement and areas of stricture
• Characteristic Findings– Mucosal nodularity– Narrowed lumen– Ulceration– String sign– Abscesses or fistula
• String Sign– Term often applied to the appearance of any
marked narrowing of the lumen, but originated as descriptor of reversible narrowing in Crohn disease.
– Narrowing caused by incomplete filling as result of irritability/spasms associated with ulceration.
String Sign
Masselli G. The gastrointestinal string sign. Radiology. 2007 Feb;242(2):632-3.
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Extraintestinal ManifestationsExtraintestinal Manifestations
• Dermatologic features: erythema nodosum, pyoderma gangrenosum
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Extraintestinal ManifestationsExtraintestinal Manifestations
• Ocular: episcleritis, anterior uveitis
• Rheumatic: arthritis, ankylosing spondylitis, sacroiliitis
• Hepatobiliary: steatohepatitis, cholelithiasis, primary sclerosing cholangitis
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Feature UC CDDepth of inflamation Mucosal TransmuralPattern of disease Contiguous Skip areasLocation Colorectal Mouth-
AnusRectal involvement Usual less commonIleal disease Backwash 10-15% CommonFistulas Rare CommonPerianal Disease Rare CommonGranulomas Unlikely 10-30% ptsOvert Bleeding Usual less commonMalnutrition Unlikely more commonCancer Risk CRC, Cholangio CRC,Sm BwlTobacco use Protective Harmful
Features of UC versus CDFeatures of UC versus CD
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Laboratory testingLaboratory testing
• CBC (high rate of anemia, due to chronic inflamm., blood loss, B12 malabsorption)
• ESR, CRP often elevated• Albumin (often low due to chronic inflamm.,
blood loss, malabsorption)• Stool studies to rule out infection• Noncaseating granulomas on biopsy suggest
CD
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ImmunoPathogenesis of UCImmunoPathogenesis of UC
Bogdanos and Polymeros Gastroentrol 2004Sartor Nat Clin Pract Gastroenterol Hepatol 2006, Stephen Gastr Hepatol 2009Bamias Cur Opin Gastroenterol 2013
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Immunology and Cytokines in IBD: A Basic DichotomyImmunology and Cytokines in IBD: A Basic Dichotomy
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ImmunoPathogenesis of UCImmunoPathogenesis of UC
Strobe and Fuss Gastroenterol 2013
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Immunology of Chron’s diseaseImmunology of Chron’s disease
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Autoantibodies in Crohn‘s diseaseAutoantibodies in Crohn‘s disease(Auto)antibodies to glycans specific for Crohn’s disease
ASCA, Main et al., 1988
anti-chitobioside carbohydrate ab (ACCA)
anti-laminaribioside carbohydrate ab (ALCA)
anti-mannobioside carbohydrate ab (AMCA)
ELISA, Altstock et al., 2005
Antibodies to bacterial antigensOuter-membrane porin of E.coli (OmpC),
Flagellin CBir1
Pseudomonas fluorescens ass. Sequence I2
Pancreatic autoantibodies - autoantibodies to exocrine pancreas30% Crohn’s disease patients
indirect immunofluorescence, Stöcker et al., 1984
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Clumpy staining Clumpy staining in the lumen of in the lumen of pancreatic acinarpancreatic acinartype 1type 1
Speckled cytoplasmic Speckled cytoplasmic staining in pancreatic staining in pancreatic acinar cells, type 2acinar cells, type 2
Pancreatic autoantibodies, type 1 and type 2Pancreatic autoantibodies, type 1 and type 2
Stöcker W et al., 1987 Scand J GastroenterolBogdanos Autoimmun Rev 2011
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type I stainingtype II staining
PAB, type 1 and type 2
Pancreatic acinus
Roggenbuck D et al., 2013 Adv Clin ChemKomorowski L et al., 2012 JCC
Bogdanos Autoimmun Rev 2011Pavlidis Clin Dev Immun 2013
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Is there any connection between Is there any connection between Pancreas and Colon in IBD?Pancreas and Colon in IBD?
Pavlidis and Bogdanos Clin Dev Immun in pressRoggenbuck Adv Clin Chem 2013Bogdanos and Forbes Clin Dev Immun 2013
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Identification of PAB target
Two-dimensional electrophoresis and immunoblot
Roggenbuck D et al., 2009 Gut
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GP2 specific IgG and IgA in patients with PAB-positive and PAB-negative CD, UC, and blood donors detected by IIF using GP2 transfected HEK293 cells
Patients IgG IgA
PAB-positive CD 42 28 (66%) 18 (43%)
PAB-negative CD 31 0 0
Ulcerative colitis 49 1 (2%) 0
Blood donors 69 1 (1%) 0
IFT huGP2 in HEK293
Roggenbuck D et al., 2009 Gut
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MALDI-TOF mass spectrometry:GP2, zymogen granule glycoprotein 2
Identification of PAB target
Roggenbuck D et al., 2009 Gut
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Physiological role of GP2
not fully understood yet
homology to Tamm-Horsfall protein (uromodulin)
first line defense against microbial agents
Interaction with type 1 fimbriae of E.coli (FimH)
Transcytotic receptor in M cells – regulation of innate and acquired immunity
GP2 in human intestine
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Hase K et al., 2009 Nature
GP2 – M cell receptor
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Ohno and Hase., 2010 Gut Microbes
Peyer‘s patches
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Peyer‘s patches
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First confirmation of GP2 in human intestine, the side of inflammation in IBD
Pancreatic autoantigen: GP2 in human intestinePancreatic autoantigen: GP2 in human intestine
A CD, n=4B CU, n=4D controls, n=5
* p<0.02
*
*
Roggenbuck et al., 2009 GutPavlidis Gut 2012
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Thus the pancreatic GP2 autoantigen is Thus the pancreatic GP2 autoantigen is also an intestinal proteinalso an intestinal protein
Roggenbuck et al., 2009 GutPavlidis Gut 2012Liaskos Clin Dev Immunol 2013
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Peyer‘s patches
Hase K et al., 2009 Nature
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Hölzl et al., 2010 Cell Immunol
Scavenger receptor binding
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B
T
P
intestinal lumen mucosa associated lymphoid tissue
FAE
M Fim H +
Fim H +
antimicrobial IgG
D
D
GP2
Putative physiological function
Roggenbuck D et al., 2013 Adv Clin Chem
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Purification of recombinant GP2 (baculovirus expression system)
A reducing SDS-PAGEB immunoblot - anti-HISC immunoblot using anti-human GP2
1 cell culture supernatant of transfected SF9 cells2 Ni-chelate chromatography3 anion exchange chromatography on Mono Q
Roggenbuck et al., 2011 Clin Chim Acta
Expression of recombinant GP2
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A: PAB-positive CD patients (n = 72)B: PAB-negative CD patients (n = 106)C: UC patients (n = 100)D: BD (n = 162)
Anti-GP2 IgG ELISA
Roggenbuck and Bogdanos 2011 Clin Chim Acta
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A: PAB-positive CD patients (n = 72)B: PAB-negative CD patients (n = 106)C: UC patients (n = 100)D: BD (n = 162)
Anti-GP2 IgA ELISA
Roggenbuck, Bogdanos et al., 2011 Clin Chim Acta
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Disease phenotype in CD
Montreal classification* CD (n = 169) UC (n= 102)
Female, n (%) 102 (60.3) 57 (55.9)
Mean age at study (max,min) 36 (8,87) 47* (17,92)
Age at diagnosis (years) (SD)
below 16 years (A1), n (%) 31 (18.3)
between 17 and 40 years (A2), n (%) 19 (11.2)
above 40 years (A3), n (%) 119 (70.4)
Location
ileal (L1), n (%) 24 (14.,2)
colonic (L2), n (%) 32 (18.9)
ileocolonic (L3), n (%) 113 (66.9)
upper disease, modifier (L4), n (%) 12 (7.1)
Bogdanos et al., 2012 BMC Gastroenterol
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CD (n = 169) UC (n= 102)
Behavior
non-stricturing, non-penetrating (B1), n (%) 86 (50.9)
stricturing (B2), n (%) 41 (24.3)
penetrating (B3), n (%) 42 (24.8)
perianal disease modifier (p), n (%) 62 (36.7)
non-stricturing, non-penetrating (B1p) ,n (%) 20 (11.8)
stricturing (B2p), n (%) 11 (6.5)
penetrating (B3p), n (%) 31 (18.3)
Disease phenotype in CD
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CD
(n = 169)
UC
(n = 102)
number of positive
antibodies by 4 ELISAs
0 83 (49.1) 87 (85.3)
1 40 (23.7) 12 (11.8)
2 28 (16.6) 3 (2.9)
3 11 (6.5) 0 (0.0)
4 7 (4.1) 0 (0.0)
Prevalence of CD specific Ab
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Association with disease location
Disease phenotype in CD
Bogdanos et al., 2012 BMC Gastroenterol
* ** * *
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Association with disease location
Disease phenotype in CD
Pavlidis et al., 2012 Clin Dev Immunol 2012
P = 0.0128
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Association with disease behavior
Disease phenotype in CD
Bogdanos D et al., 2012 BMC GastroenterolRoggenbuck D et al., 2012 JPGNRieder F et al., 2012 Gastroenterol
*
*
*
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Association with disease activity
Correlation with disease activity?Similarity to anti-ASGPR in autoimmune hepatitis serology
At diagnosis
2 months on immunosuppressive Tx
3 mo on Tx 12 mo
on Tx
36 moon Tx
60 moon Tx
Rigopoulou et al., 2012 Autoimmun RevRoggenbuck et al., 2012 Autoimmun Highlights
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Liaskos Autoimmun 2013
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Liaskos Autoimmun 2013
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Per
cen
t ex
pre
ssio
n
GP2 expression
10
20
30
40
50
unstimulated CD3 activated
unstimulated CD3 activated
GP2
β actin
*
GP2 expression on PBMCs
Werner et al., 2012 J Immunol
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***
Apoptosis
T84hIECs
10
20
30
40
50
0 10ug/ml 20ug/ml
GP2
Per
cen
t A
nV
+P
I-p
osit
ive
cell
s
GP2 effect on epithelium
Werner et al., 2012 J Immunol
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***
*
Proliferation
0.2
0.4
0.6
0.8
1
0 10ug/ml 20ug/ml
GP2
O.D
.
T84hIECs
GP2 effect on epithelium
Werner et al., 2012 J Immunol
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**
90100110120130140150160170180
0 5ug/ml 10ug/ml
Epithelial T84Monocytes
Per
cent
eff
ect *
GP2:
GP2 – phagocytosis of E-coli
Werner et al., 2012 J Immunol
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20
40
60
80
0 10 ug/ml
PBMC
PBMC-Treg
PBMC-Treg+Treg
Per
cen
t C
D3+
CD
25+
pos
itiv
e ce
lls
GP2
Activation
*
*
Depletion of Tregs - GP2 effect
Werner et al., 2012 J ImmunolPavlidis JCC 2013Liaskos Clin Dev Immunol 2013
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10
20
30
40
0 10 ug/ml
Per
cen
t A
nV
+P
I-p
osit
ive
cell
s
Apoptosis
** PBMC
PBMC-Treg
PBMC-Treg+Treg
GP2
Depletion of Tregs - GP2 effect
Werner et al., 2012 J Immunol
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CD3 - + + + +
GP2 - - + - +
IFX - - - + +
10
20
30
40
50
10
20
Per
cen
t C
D3+
CD
25+
pos
itiv
e ce
lls
Per
cen
t A
nV
+P
I-p
osit
ive
cell
s
*
**
*
*
*
Apoptosis
Activation
antiTNFa modulates GP2
Werner et al., 2012 J Immunol
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Untreated CD3 +ADACD3 +IFXCD3
GP
2β-
Act
in
Untreated
100
101
102
103
104
13.6% 30.1% 21.7% 20.9%
100
101
102
103
104
100
101
102
103
104
100
101
102
103
104
060
120
Cou
nts
060
120
060
120
060
120
GP2/SA-FITC
antiTNFa modulates GP2
PBMCs (N=3) were stimulated with anti-CD3 and Caco2 cells (N=3) with 10 µg/ml LPS. Cells were incubated either with or without 10 µg/ml IFX or ADA. RNA levels were determined using PCR. Surface expression was determined using flow cytometry.
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B
T
P
intestinal lumenmucosa associated lymphoid tissue
FAE
Fim H +
Fim H +
anti-GP2 IgG
D
D
anti-GP2 IgA
Fim H +
M
M
M
Putative pathophysiology
Roggenbuck D et al., 2013 Adv Clin Chem
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Take-home message
Summary
GP2 is a target of PAB in CD
GP2 is expressed in human intestine, transcytotic receptor of M cells
IgA and IgG anti-GP2 detected by novel ELISA are specific for CD
Anti-GP2 detection may improve serological diagnosis of CD
![Page 57: Dimitrios P. Bogdanos Professor of Immunopathology The Sheila Sherlock Medalist Autoimmunity in Inflammatory Bowel Diseases.](https://reader033.fdocuments.us/reader033/viewer/2022051516/56649d0b5503460f949de04c/html5/thumbnails/57.jpg)
Take-home message
Summary
Anti-GP2 antibodies are associated with clinical phenotype in Crohn’s disease
Anti-GP2 IgA and IgG were more prevalent in CD:
at a younger age (A1),
with ileocolonic location (L3),
stricturing behaviour (B2)
GP2 modulates innate and adaptive immune mechanisms
![Page 58: Dimitrios P. Bogdanos Professor of Immunopathology The Sheila Sherlock Medalist Autoimmunity in Inflammatory Bowel Diseases.](https://reader033.fdocuments.us/reader033/viewer/2022051516/56649d0b5503460f949de04c/html5/thumbnails/58.jpg)
Is there any connection between Is there any connection between Pancreas and Colon in IBD?Pancreas and Colon in IBD?
YES THERE IS YES THERE IS
Pavlidis and Bogdanos Clin Dev Immun in pressRoggenbuck Adv Clin Chem 2013Bogdanos and Forbes Clin Dev Immun 2013
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Special thanks to my close friend Dirk Roggenbuck for the artwork
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Thank you for your attention!