Induction of pathogenic vs. regulatory T cells depends on APC /T cell interactions CD-80 CD-86 CD-28 CTLA-4 MHC TCR MHC TCR Ag Ag CD 40 CD 40 L IL-10 IFNIL- 12,18, 23 IL-10 TGFIFNIL-17 TH 1, 17 TR 1, T H3 T reg Antigen presenting cells (APC) process and present bacterial antigens, are activated by bacterial adjuvants CD-80 CD-86 CD25 TGFEffector (microbial clearance, inflammation) Regulatory (homeostasis)
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Induction of pathogenic vs. regulatory T cells depends on APC /T cell interactions CD-80 CD-86 CD-80 CD-86 CD-28 CTLA-4 MHC TCR MHC TCR Ag CD 40 CD 40.
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Induction of pathogenic vs. regulatory T cells depends on APC /T cell interactions
CD-80CD-86CD-80CD-86
CD-28CD-28
CTLA-4CTLA-4MHCMHC
TCRTCR
MHCMHC
TCRTCRAg
AgCD40CD40
CD40LCD40L
IL-10IFNIL-10
IFNIL-12,18, 23
IL-12,18, 23
IL-10TGFIL-10TGF
IFNIL-17IFNIL-17 TH1, 17TH1, 17
TR1, TH3
Treg
TR1, TH3
Treg
Antigen presenting cells (APC)process and present bacterial
Aggressive early onset Crohn’s disease in IL-10 receptor deficient families
•Immune cells from these patients were hyper-responsive to bacterial products and did not respond to IL-10 suppression
•One patient with refractory disease had complete remission with a bone marrow transplant from a sibling who lacked this gene (corrected genetic defect in immune cells)
Glocker, NEJM 2010
Pro-inflammatoryPro-inflammatory
Anti-inflammatoryAnti-inflammatory
TNFIL-1IL-6
IL-12 / 18 / 23IL-4,
IFNIL-ILIL-21
TNFIL-1IL-6
IL-12 / 18 / 23IL-4,
IFNIL-ILIL-21
IL-10TGF
IL-1Ra, IL-11IFN
PGE2, PGJ2
IL-10TGF
IL-1Ra, IL-11IFN
PGE2, PGJ2
Loss of tolerance(Inflammation)
Loss of tolerance(Inflammation)
Tolerance(Homeostasis)
Tolerance(Homeostasis)
Selective Correction of Mediator Selective Correction of Mediator ImbalanceImbalance
Therapeutic Manipulation of Intestinal Bacteria (individual profile): Selectively Alter Beneficial vs. Detrimental Species
Injurious Pro-inflammatory
Bacteroides vulgatus, B. thetaEnterococcus faecalis
E. coli - enteroadherent / invasive
Klebsiella pneumoniaeBifidobacterium animalis
Fusobacterium variumIntestinal Helicobacter species
New Paradigm for Treating Subsets of IBD patients: Match the aggressiveness of treatment with the predicted
aggressiveness of disease
Moderate
Severe/refractory
Mild
Predicted diseaseactivity
Get it right the first time!
Contrasting current approaches to treating IBD and cancer
IBD
• Assess location and extent of disease
• Treat all patients the same (bottom up or top down), with some variation for aggressiveness
Generic approach (30-40% remission rate, no cure)
Cancers
• Check genotype (prognosis, treatment guide and family screening)
• Clinical, imaging assessment of extent (aggressiveness, clinical pattern)
• Analyze tissue for receptor expression, enzyme levels, histologic grade of aggressiveness/differentiation, depth of extension (results determine which therapy used, prognosis)
Targeted /individualized approach expectations of cures
IBD1 IBD2 IBD3 IBD4
CDUC
Disease behavior, mechanisms
Names vs. Mechanistic subsetsNames vs. Mechanistic subsets
Defining IBD: current vs. future
From Dermot McGovern
Individualizing therapy for IBD subtypes: Different mechanisms, different features, different therapies
Genetic Genetic mutationsmutations
NOD2
ATG16L1
IL-23R
Gene (s) IV
ClinicalClinicalPhenotypePhenotype
CD I-aggressive SB dz
SB dz?
course
CD II
CD IVfistula
Immunologic Immunologic response to response to
bacterial antigenbacterial antigen
ASCA, OmpC,
I2+
?
?
Flagellin
ClinicalClinical
IBD I-aggressive SB dz
IBD IIIMild
SB dz
IBD II-UC-like
IBD IV?
ClinicTreatment
Rx 1?defensinsAntibiotic
GM-CSFAntibx?
Anti- IL-23(?)
Therapy 4
How to predict which patient will:
• Have an aggressive course?• Respond to a potential treatment?• Have complications of disease or therapy?
Understand mechanisms of disease in an individual at time of diagnosis
Genetic, microbial, immunologic profiles and clinical phenotype
Pediatric Research Network• Investigating unique needs of children and adolescents with IBD• 28 centers have enrolled 1800 newly diagnosed patients with IBD
bacteria, genes and clinical features that predict at the time of diagnosis which child will develop severe, complicated vs. mild Crohn’s disease and which individual will respond to each medication
Clinical Implications: When a patient is diagnosed, initiate treatment with a medication that will almost certainly work well, prevent complications with aggressive therapy in patients with high risk of aggressive disease courses and complications, but use nontoxic drugs for low risk pts: minimize drug toxicity and cost
2 patients with Crohn’s disease, 2 different
treatments (2020)Patient A:• Tissue shows low F. prausnitzii, high AI E. coli• Genotype – NOD 2 polymorphism• Treatment: Ciprofloxacin x 1 month, F. prausnitzii probiotic
weekly, daily plantain extract (prevent AIEC binding) (backup- early resection and prevent recurrence with F. prausnitzii probiotic )
• No clinical symptoms or Rx complications for 15 yearsPatient B:• Genotype IL-23R polymorphism• Treatment: prolonged administration anti- IL-23 antibody
(backup: bone marrow transplant from sibling without IL-23R gene defect)
• No further Crohn’s disease symptoms for 15 yrs
What needs to be done to cure a patient with IBD?
1. Understand mechanisms of disease in an individual Genetic, microbial, immunologic profiles and clinical phenotype
2. Fix the problem
• Correct underlying defective pathway
OR
• Permanently block inflammatory response
Nontoxic medication that induces a sustained, complete remission
CCFA Initiatives that can help develop new approaches to correcting causative IBD defects
• Genetics- Determine function of major IBD risk genes (now 163 total) and how the abnormal genes and pathways interact. Once abnormal mechanisms are identified, strategies to correct them with new or existing medications can be developed
• Microbiome: Identify key causative and protective bacterial species and infectious triggers. Once identified, realistic strategies to eliminate/ block detrimental species, augment concentration or function of protective species, and avoid triggering agents (? Immunization) can be developed
What needs to be done to prevent onset of IBD in a high risk individual?
1. Identify which person is at risk of developing IBD
Genetic, microbial, immunologic profiles
2. Fix the problem
• Correct underlying defective pathway
OR
• Eliminate environmental triggers
• Alter microbial profile
• Alter immune response
In 2014, we have built the foundation to better understand the role of microbiota in intestinal diseases.
Can we use this information to:
• Treat disease or prevent relapses by manipulating the environment (altering diet, environmental, triggers, bacteria, fecal transplant)?
• Deliver optimal individual treatment based on clinical features and genetic, microbial and immunologic profiles?
• Cure patients with disease by correcting defects or permanently normalizing responses?
• Prevent disease in susceptible individuals by manipulating their environment or correcting the underlying defect?
Individualizing therapy for IBD subtypes: Different mechanisms, different features, different therapies
Genetic Genetic mutationsmutations
NOD2
ATG16L1
IL-23R
Gene (s) IV
ClinicalClinicalPhenotypePhenotype
CD I-aggressive SB dz
SB dzPost-op
recur course
CD II
CD IVfistula
BacterialBacterialprofileprofile
Adh/inv
E. coli
Klebs
F. prausnit
Claustrid
ClinicalClinical
IBD I-aggressive SB dz
IBD IIIMild
SB dz
IBD II-UC-like
IBD IV?
ClinicTreatment
Rx 1 block piliAntibiotic
GM-CSFAntibx
Anti-IL-23
F. prausnitzi
ReplaceClaustrid
Sequential, safer approach to treating IBD: Maintain long term remission by alternative approaches
acid, vit D acid, vit D Bacteroides fragilis PSA. Bacteroides fragilis PSA. Clostridium subsetsClostridium subsets, , F. prausnitziiF. prausnitzii, worms, worms
Promote Promote regulatory cellregulatory cell
activity activity ((TRTR11, TH, TH33 , Treg, , Treg, B cells, DC) B cells, DC)
acid, vit D acid, vit D Bacteroides fragilis PSA. Bacteroides fragilis PSA. Clostridium subsetsClostridium subsets, , F. prausnitziiF. prausnitzii, worms, worms