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Gliadin Antibodies IgA, IgG, Endomysial Antibodies, Celiac disease and Sprue

March 5, 2024Immune systemLab Tests

Table of Contents

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  • Gliadin Antibodies IgA, IgG
        • What sample is needed for Gliadin Antibodies IgA and IgG?
        • What are the Indications for Gliadin Antibodies IgA and IgG?
      • What are the precautions for Gliadin Antibodies?
        • How will you define Celiac disease/Sprue?
        • How will you differentiate between Celeic disease and sprue?
        • How will you discuss the epidemiology of Celiac disease?
        • How will you discuss the pathogenesis of Celiac disease and sprue?
        • What are the auto-antigens of Celiac disease?
        • What antibody forms in Celiac disease?
        • What are the pathological changes in Celiac disease?
        • What are the signs and symptoms of Celiac disease?
        • What are the complications of Celiac disease?
        • What is the normal Gliadin-antibody?
        • How will you diagnose celiac disease?
        • What are the serological tests for Celiac disease?
      • What are the diagnostic criteria for the Celiac disease
        • How will you treat Celiac disease?
      • Questions and answers:

Gliadin Antibodies IgA, IgG

What sample is needed for Gliadin Antibodies IgA and IgG?

  1. Collect the venous blood to prepare the serum.
  2. A fasting sample is not necessary.
  3. An intestinal biopsy may be advised, and it gives characteristic changes.

What are the Indications for Gliadin Antibodies IgA and IgG?

  1. These antibodies are detected in gluten-sensitive enteropathy.
  2. This test is done to diagnose Celiac disease and sprue.
  3. These antibodies are used to monitor the disease.
  4. In successful treatment with a gluten-free diet, these antibodies will disappear from the serum.

What are the precautions for Gliadin Antibodies?

  1. Other gastrointestinal diseases like colitis, Crohn’s disease, and lactose intolerance can raise the value of Gliadin antibodies.
  2. Get the list of foods eaten in the last 24 hours.

How will you define Celiac disease/Sprue?

  1. It is also called Celiac disease, Gluten-sensitivity enteropathy, nontropical sprue, or idiopathic steatorrhea.
  2. Gluten-induced enteropathy includes Sprue and Celiac disease.
    1. Both these diseases involved duodenum and jejunum predominantly.
  3. The celiac disease is sometimes called non-tropical sprue, celiac sprue, or gluten-sensitive enteropathy.
    1. Celiac disease is an autoimmune multisystem disease.
    2. Celiac disease is also called childhood non-tropical sprue.
    3. A gluten-free diet cures the celiac disease.
  4. The sprue is an infectious process that is cured by antibiotics.
    1. Sprue is a broad, nonspecific term that describes several conditions characterized by malabsorption affecting the small intestine.
    2. Sprue can be referred to as nonspecific celiac disease and is also known as celiac sprue.
    3. It also includes tropical sprue and non-celiac gluten sensitivity.
    4. Tropical sprue is similar to celiac disease, but it occurs in tropical regions with different underlying causes.
    5. In short, Sprue is a broad term, including celiac disease and other conditions with similar symptoms and malabsorption.

How will you differentiate between Celeic disease and sprue?

Parameters Celiac disease Sprue
  • Known as
  1. Non-tropical sprue or Gluten-sensitivity
  2. Childhood non-tropical sprue
  1. It is an infectious process
  2. It is a non-specific term
  3. Known as Celiac sprue
  • Mechanism
  1. Autoimmune phenomenon
  • It is an infectious process
  • Cured by antibiotics
  • Signs and symptoms
  1. Multisystem disease
  2. Malabsorption
  1. Occurs in tropical region
  2. Malabsorption
  • Treatment
  1. Avoid gluten
  2. Gluten-free does cure the disease
  1. Antibiotics

How will you discuss the epidemiology of Celiac disease?

  1. It is found predominantly in Europe and, uncommonly, in African -America.
  2. It is rare in Asia.
  3. It is 10 to 15 times more common in IgA-deficient persons.
  4. It is 1% to 3% in patients with diabetes mellitus type 1.
  5. There is an association between T-cell lymphoma and juvenile rheumatoid arthritis.

How will you discuss the pathogenesis of Celiac disease and sprue?

  1. Celiac disease is also called Gluten-sensitive enteropathy, Nontropical sprue, or idiopathic steatorrhea.
  2. Meanwhile, sprue is a broad term characterized by malabsorption, like Celiac disease.
  3. Gliadin is the toxic protein of gluten

What are the auto-antigens of Celiac disease?

  1. Gliadin is the complex of gluten and tissue transglutaminase.
  2. Tissue transglutaminase is present in the thin connective tissue covering the muscles.
    1. Gliadin is the toxic protein of the gluten.
    2. Gluten = Gliadin + tissue transglutaminase.
    3. The small bowel (mainly duodenum and jejunum) tissue Transglutaminase is the auto-antigen.
  3. Pathogenesis of the disease is believed to involve an interaction between transglutaminase and the gliadin peptide in genetically susceptible people.
  4. In both conditions (celiac disease and sprue), T-lymphocytes mediate an immune reaction against gluten.
    1. Gluten is found in wheat, rye, barley, and maybe oats.
  5. There is a genetic predisposition, and it runs in families.
  6. 10% of the first-degree relatives have this disease.
  7. There is an association in HLA-DR3  in 90% of the patients and the same for dermatitis herpetiformis.
    1. Another reference says a genetic component is present in the HLA chromosome 6.
  8. The major toxic protein of wheat is gliadin.
  9. There is sensitivity to Gliadin (gluten), which are the proteins found in:
    1. Wheat.
    2. Wheat products.
    3. Rye.
    4. Barley.
    5. Possible oats.

What antibody forms in Celiac disease?

  1. Antibodies to gliadin are toxic agents in celiac disease.
  2. Patients with celiac disease cannot tolerate the proteins gliadin + gluten in wheat or wheat products.
  3. Gliadin + gluten is toxic to the small intestinal mucosa and leads to characteristic pathologic changes seen on biopsy.
  4. Endomycelium: It is a thin layer of connective tissue surrounding the muscle.
  5. These patients develop antibodies against:
    1. Gliadin = anti-gliadin antibody (IgA and IgG)
    2. Endomysial = anti-endomysial antibody.
    3. Tissue = anti-tissue transglutaminase.
Celiac disease mechanism

Celiac disease mechanism

  1. These patients have severe intestinal malabsorption.
  2. The only treatment for these patients is to avoid wheat and wheat products.
  3. These antibodies are present in the mucosa and the blood.
  4. The celiac disease starts in infancy when cereals are given to the baby.
  5. IgG-antigliadin antibody is more sensitive but less specific than IgA.
  6. Anti-gliadin antibodies are found in 95% of those with Celiac disease and nontropical sprue.
    1. Anti-IgG gliadin antibodies are found in 96% to 97% of untreated patients. 80% may have Celiac disease.
    2. Anti-IgA gliadin antibodies are found in 75% of the cases, and these are 95% specific for Celiac disease.
    3. Anti-gliadin antibodies IgG and IgA are positive in 45% to 85% of dermatitis herpetiformis.
    4. False positive cases are seen in ulcerative colitis and Crohn’s disease.
Endomysial antibody formation

Endomysial antibody formation

What are the pathological changes in Celiac disease?

There are typical changes on the intestinal (jejunal)  biopsy like:

  1. There is villous atrophy.
  2. Goblet cells are decreased or absent.
  3. It shows crypt hyperplasia.
  4. Intestinal epithelial cells show vacuoles.
    1. The intestinal mucosa first shows blunting of the mucosal villi. . There is mild widening and shortening.
    2. It is followed by flattening and loss of villi.
  5. There is a lymphocytic infiltrate in the mucosa and submucosa. Also, these cells will infiltrate the lamina propria.
Gliadin Antibodies IgA: Pathological changes of Celiac disease

Gliadin Antibodies IgA: Pathological changes of Celiac disease

What are the signs and symptoms of Celiac disease?

  1. Mostly, the symptoms are seen in children when they start cereals.
  2. The most common presentation is:
    1. There is easy fatigability.
    2. There is abdominal bloating and pain.
    3. There may be vomiting.
    4. The patient will have chronic diarrhea.
      1. The stool is foul-smelling, pale, and fatty.
      2. Sometimes, these patients will be constipated.
      3. The stool is hard to flush.
    5. There are aphthous ulcers.
    6. The patient will have weight loss.
    7. These children are irritable.
    8. Delay in the growth pattern.
    9. Sometimes, it is difficult to thrive, and the patient may have osteomalacia.
    10. There is a strong association with other autoimmune diseases like diabetes mellitus type 1 and autoimmune thyroid diseases.

What are the complications of Celiac disease?

  1. There is anemia.
  2. 15% to 20% of patients develop intestinal lymphoma or adenocarcinoma.
  3. There is an increased incidence of gastric and esophageal carcinoma.
  4. There may be neuropathy.
  5. These patients may have hyposplenism.

What is the normal Gliadin-antibody?

  • Values are given for the child of age >2 years:
    • Negative = < 25 U/L .
    • weak positive = 25 to 50 U/L.
    • Positive = >50 U/L.

Source 6

  • Gliadin IgA/IgG = 0 to 2 years = <20 EU.
    • 0 to 3 years and older = <25 EU.
  • Endomysial IgA = all ages = negative.
  • Tissue transglutaminase IgA = all ages = <20 EU.

How will you diagnose celiac disease?

  1. An elevated level of anti-gliadin and anti-endomysial antibodies.
  2. IgA and IgG antibody sensitivity are 90% for the active untreated disease. When both antibodies are done, the specificity is also 90%.
  3. These antibodies will detect the following:
    1. Celiac disease will 100% have IgA endomysial antibodies.
    2. Celiac sprue.
  4. Dermatitis herpetiformis 70% shows IgA endomysial antibodies.
  5. Intestinal (jejunum) biopsy shows typical changes in villous atrophy.
    1. On jejunal biopsy, we will see villous atrophy.
    2.  Increased intra-epithelial lymphocytic infiltrate.
    3. There is hyperplasia of the crypts.
      1. These changes may reverse on a gluten-free diet. This will not occur in the sprue.
  6. In Celiac disease, anemia may be either macrocytic or hypochromic microcytic anemia.

What are the serological tests for Celiac disease?

Antibody Specificity Sensitivity
IgA- antigliadin antibody 95% 75% to 95%
IgA- endomysial antibody >99% 80% to 100%

What are the diagnostic criteria for the Celiac disease

  1. Provisional diagnosis:
    1. Positive serological (anti-gliadin antibody) test.
    2. Typical pathological findings on biopsy of the small intestine.
  2. The confirmatory test is:
    1. When a gluten-free diet is given, then patients become symptom-free.
    2. Serological tests become in the normal range or negative.
    3. The pathological changes will improve or disappear if a biopsy is done.

How will you treat Celiac disease?

  1. Start a permanently gluten-free diet.
  2. Avoid wheat, barley, rye, and oats.
    1. Another reference excludes oats, which are allowed in the list of eatable foods. Be sure there is no wheat, barley, or rye mixing.
  3. Or any food containing them, like bread, cake, and pies.
  4. Rice, soya, potatoes, maize, jam, and sugar are allowed.
  5. Gluten-free flour, bread, and pasta are available.
  6. Try steroids if diet therapy is not helpful.

Questions and answers:

Question 1: What are the false positive conditions for Anti-gliadin antibodies?
Show answer
False positive results may be seen in ulcerative colitis and Crohn's disease.
Question 2: What is the result of Celiac disease?
Show answer
When a gluten-free diet is given, Celiac disease will be cured.

Possible References Used
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