Slide 1 - Clinical Immunology Society

بسم الله الرحمن بسم الله الرحمن الرحيمالرحيم

Immunological Basis of

Gastrointestinal Disorders

Maha A. El BassuoniAss.Prof. of Clinical Pathology

Faculty of Medicine , Menoufiya University, EGYPT

The immune System

The cells and molecules responsible for immunity

constitute the immune system.

The immune system has to be able to respond to protect the human body from a very large number of foreign antigens introduced at any site.

Mucosal Immune System The mucosal immune The mucosal immune

system is recognized by system is recognized by differences from its differences from its systemic counterpart.systemic counterpart.

It is recognized that the It is recognized that the mucosal immune mucosal immune response is also distinct, response is also distinct, largely focused on largely focused on suppressing immunity suppressing immunity rather than promoting it.rather than promoting it.

Gut Associated Lymphoid Tissue(GALT)

Structure of Secretory IgA

It consists of at least two IgA molecules covalently linked by a J chain and the secretory component, which is added as the antibody crossed the mucosal epithelial cells into the lumen..

Gastrointestinal Organs Disorders

A. Gastrointestinal Disorders

B. Pancreatic Disorders

C. Hepatobiliary Disorders

D. Orodental Disorders

A. Gastrointestinal Disorders1. Food -Induced Gastrointestinal Disorders

I. Gluten-sensitive Enteropathy Celiac Disease

Endomysial antibodies on smooth muscleEndomysial antibodies on smooth muscle


I. Gluten-sensitive Enteropathy Celiac Disease

Laboratory Investigation:Laboratory Investigation: Hypoalbuminemia Hypoalbuminemia

hypoproteinemiahypoproteinemia

Iron, folate, and, vB12 Iron, folate, and, vB12 deficiency.deficiency.

PT prolongedPT prolonged

circulating IgA and IgG to circulating IgA and IgG to gliadin gliadin

IgA antibody to endomysium IgA antibody to endomysium has higher sensitivity and has higher sensitivity and specificity specificity

Allergy is an immunological phenomena

refers to certain diseases in which immune responses to environmental antigens causes tissue inflammation and organ dysfunction.

Hypersensitivity and Sensitivity used as synonyms for allergy.


II. Gastrointestinal food allergy diseases



a. Dietary Protein-Induced Proctitis/Proctocolitis eosinophilic infiltration and occasionally lymph-nodular

hyperplasia. b. Dietary Protein Enteropathy T cell responses

c. Dietary Protein Enterocolitis milk-specific T cell response

d. Immediate Gastrointestinal Hypersensitivity mediated by IgE antibody

e. Eosinophilic Gastroenteropathiesboth cell-mediated and IgE antibody-mediated

d. Immediate Gastrointestinal Hypersensitivity Allergy testingAllergy testing

In vitro testsIn vitro tests Tests for IgE Abs (RAST).Tests for IgE Abs (RAST). Tests for IgG Abs .Tests for IgG Abs . Tests for Immune complex.Tests for Immune complex. Tests for Lymphocyte Tests for Lymphocyte

stimulationstimulation

Antigen cross links IgE on mast cells in tissues Mast Cell Degranulation



2. Chronic Atrophic Gastritis

Normal AtrophicNormal Atrophic

A. Gastrointestinal Disordes

2. Chronic Atrophic Gastritis Autoimmune Atrophic Gastritis (Type A)


2. Chronic Atrophic Gastritis Autoimmune Atrophic Gastritis Types of intrinsic factor antibodies


2. Chronic Atrophic Gastritis Autoimmune Atrophic Gastritis

Diagnosis of autoimmune gastritis however, it can be ascertained histologically:

(1) Antiparietal and anti-IF antibodies in the serum.

(2) Achlorhydria and hypergastrinemia

(3) serum v. B12 levels, usually low.

Anti-Parietal Cells (Rat stomach)


2. Chronic Atrophic Gastritis Gastric autoantibodies

ConditionParietal Cell Antibody

Intrinsic Factor Antibody

Pernicious Anemia Serum 90%IgG – 65%IgA – 25% IgG

Gastric Juice 70%IgA

Blocking Type 70% , IgG Binding Type 35% IgA

Relatives of patients with PA

30% <1%

Other autoimmune diseases Thyroid disease Diabetes mellitus Addison's disease

20% 5%

Iron Deficiency anemia 25% <1%

Healthy Adults Females >60 years

<20 years10%

2%

<1%

<1%

A. Gastrointestinal Disorders 3.Human immunodeficiency Virus Enteropathy

HIV infection HIV is one of the group of viruses known as

retroviruses.

When HIV infects a human cell, its RNA has to be converted to DNA.

It exerts its effect both directly, through infection of the intestinal cells and indirectly through impairment of the intestinal immune response.

The antigenicity of various components provides a means for detection of antibody, and the basis for most HIV testing.

HIV Virus Lifecycle

Gastrointestinal Disorders 4.Whipple's Disease

DiagnosisDiagnosis microscopic examination of microscopic examination of

specimens. The established specimens. The established cultivation of the bacterium and cultivation of the bacterium and the isolation from infected the isolation from infected intestinal biopsies intestinal biopsies

PCR analysis, which has high PCR analysis, which has high sensitivity and specificity. sensitivity and specificity.


5. Inflammatory Bowel Diseases I. Crohn's Disease II. Ulcerative colitis


5. Inflammatory Bowel Diseases



Enteric bacterial flora has been reported in both animal models and IBD patients.

In animal models Oslon et al have reported that CD4+CD45RBloCD25+ regulatory T cells (Treg cells) prevent colitis induced by transferring effector CD4+CD45RBhiCD25 – T cells into SCID mice through mechanisms involving TGF-ß and IL-10.

Based on the cytotoxicity findings Sauberman et al. postulate that in mice the stimulation of NKT cells through antigen presented to these cells by CD1d-bearing DCs or epithelial cells (MHC class1-like).

The stimulated NKT cells, then

begin to produce IL-13, they become capable of lysing epithelial cells, leads to epithelial cell loss and ulceration.

B. Pancreatic Disorders

Autoimmune pancreatitis is uncommon and accounts for less than 1% of cases of chronic pancreatitis.

local expression and release of TGF-ß, enhances synthesis of extracellular matrix proteins, (collagens, fibronectin).

MCP-1mRNA IL–8 and ENA mRNA in centroacinar ducts.

Laboratory tests

↓ serum amylase and lipase only during acute attacks of pancreatitis, usually early in the course of the disease.

↓ concentrations of serum trypsin are relatively specific for advanced chronic pancreatitis. (not sensitive enough)

ANA test Fecal tests (Steatorrhea a

manifestation of advanced disease) Pancreatic function tests

C. HEPATOBILIARY DISORDERS

1. LIVER DISORDERS I. Viral HepatitisII. Autoimmune Hepatitis

2. BILIARY DISORDERS I. Primary Biliary Cirrhosis (PBC) II. Primary Sclerosing Cholangitis (PSC)


1. LIVER DISORDERS I. Viral Hepatitis HAV & HEV

Epidemics by contaminated water or food suorce

Acute HEV infection Pregnant female in 3rd trimester 25% risk of mortality


1. LIVER DISORDERS I. Viral Hepatitis HBV & HDV

Progress to cirrhosisFlare of HBV and FHF


1. LIVER DISORDERS I. Viral Hepatitis HCV

85% chronic casesAssociated with autoimmune hepatitis


1. LIVER DISORDERS II. Autoimmune Hepatitis



Autoantibodies: Autoimmune hepatitis type 1 is characterized by positive ASMA and ANA.

Type 2 marked by a positive anti–LKM-1 antibody.

Type 3 is marked by a positive anti-SLA antibody.

Anti SLAAnti SLA

Anti-actinAnti-actin

Laboratory diagnosis



Laboratory Diagnosis Hypergammaglobulinemia ↑AST and ALT ↑S. bilirubin and ALP Hypoalbuminemia and prolongation of PT Other common laboratory abnormalities

mild leucopenia Normochromic anemia Coombs-positive hemolytic anemia Thrombocytopenia


2. BILIARY DISORDERS



I. Primary Biliary Cirrhosis



I. Primary Biliary Cirrhosis

Elevation of : ALT AST ALP GGTP.

Lipid levels (HDL) and cholesterol levels may be increased .

Elevated bilirubin level Prolonged PT Decreased albumin level

The hallmark of the disease is the presence of AMAs in the sera.

AMAs found in 90-95% of patients and have a specificity of 98%.

AMA



II. Primary Sclerosing Cholangitis


2. BILIARY DISORDERS II. Primary Sclerosing Cholangitis

Laboratory Diagnosis: Increased ALP and total bilirubin, Increased transaminases Hypergammaglobulinemia, P-ANCA (65-85% of cases) ANA, (ASMA), anti-cardiolipin

autoantibodies Anti-mitochondrial autoantibodies

(AMA) are negative

P-ANCA

D. ORODENTAL DISORDERS

1. Inflammatory Periodontal Diseases

I. Gingivitis and periodentitis polymorph induced damage, complement induced damage (through IgG (IgG2). peripheral T cell reactivity to plaque antigens

II.Juvenile Periodontitis defects in granulocyte or monocyte function conventional.


2. Recurrent Aphthous Ulceration Raised level of circulating antibody to saline

extract of fetal oral mucous membrane.

These antibodies may be a response to exposed tissue antigen that previously been protected from immune system. (Ag against oral mucous membrane, epithelial cells. or viral Ags).

CMI proved by an infiltrate of lymphocyte


3.Oral Candidiasis A threshold number of systemic CD4+ cells to protect the oral

mucosa together with the status of local immunity. HIV infected persons with and without OPC had a Th2-type

salivary cytokine profile suggestive of susceptibility to Candida infection

GM-CSF are important in the generation of effective immunity to GM-CSF are important in the generation of effective immunity to C. albicansC. albicans. . .

4. Oral Hairy Leukoplakia There is correlation of diminished CD4+ T lymphocyte count to

the occurrence of the lesions.

Slide 1 - Clinical Immunology Society

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