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Cambridge Life Sciences - Immunology - Pernicious Anaemia 
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Immunology Clinical Chemistry Urease Hp Tests Instrumentation
Pernicious Anaemia

Intrinsic Factor antibodies (IFAB)

Biermer’s anaemia is the disease most frequently associated with vitamin B12 deficiency. This disease shows the classical features of megaloblastic anaemia (i.e. morphologic and functional abnormalities of the blood cells and marrow precursors related to impairment of DNA synthesis).

Pernicious anaemia is charcterised by a gastric mucosal defect that decreases the synthesis of intrinsic factor. Since this glycoprotein plays an essential role in the transport and absorption of vitamin B12 across the small intestine, patients affected by pernicious anaemia show severe decreases in serum vitamin B12 levels. The presence of auto-antibodies against gastric parietal cell cytoplasm, thyroid components and intrinsic factor, strongly suggest an auto-immune process to the disease.

Two types of anti-intrinsic factor auto-antibodies have been described. The blocking auto-antibodies (type I) hinder the binding of vitamin B12 complexes. Such antibodies are frequently encountered in patients affected by pernicious anaemia. Binding auto-antibodies (type II) that bind to the intrinsic factor as well as to the IF/vitamin B12 complexes preventing their absorbance, have also been described.

Detection of anti-intrinsic factor antibodies provides an important contribution to the differential diagnosis of pernicious anaemia (due to intrinsic factor deficiency) and other causes of vitamin B12 malabsorption. Indeed, other tests such as cytomorphology of red blood cells, determination of serum vitamin B12 levels or the Schilling test are not specific enough for the diagnosis of a Biermer’s anaemia. Anti-intrinsic factor antibodies can be detected using two types of methodologies: RIA or ELISA methods. The ability of type I auto-antibodies to prevent the binding of vitamin B12 to the intrinsic factor has allowed the development of RIA methods. Such methods, however, only detect type I auto-antibodies. Moreover, they are subject to interferences induced by exogenous sources of vitamin B12 that may induce false positive results (especially in the case of vitamin B12 treatment, or when the sample is taken after a Schilling test).

ELISA methods detect type I and type II antibodies and are unaffected by the presence of the endogenous vitamin B12 levels. The AUTOZYME™ IFAB Anti-Intrinsic Factor Antibodies Assay is an easy, rapid and sensitive method allowing the detection of total anti-intrinsic factor antibodies. The use of purified intrinsic factor as antigen ensures the specificity of the method.

AUTOZYME™ - the next generation of Enzyme Immunoassays

This assay has been designed for the modern laboratory with flexibility in mind. It can be used in manual mode or with automated instrument systems. The AUTOZYME™ system employs ready-to-use colour coded reagents resulting in less "hands on" time. Break-a-well strips ensure flexibility and economic use for any batch size so that patient turn around time can be speeded up. Kit controls coupled with high purity antigens ensure the method is valid and specific.

This format offers:

  • manual or automated methodology
  • colour-coded reagents
  • break-a-well flexibility
  • long shelf-life
  • kit controls provided
  • high purity antigens
  • rapid patient results

 

Code
Name
Description

Determinations

IFU

Z4396

Anti-Intrinsic Factor antibodies

AUTOZYME™ IFAB microwell format

96

D-tek BlueDot - Immunodot

Code
Name
Description

Determinations

IFD-24 BlueDot Intrinsic Factor IgG intrinsic factor antibody

24

IFPCAD-24

BlueDot Gastricis IgG

intrinsic factor/Parietal Cell Antigen (H+/K+ ATPase) antibody

24

For technical information on D-tek products please click here or contact us.

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Immunology     Clinical Chemistry    Urease Hp Tests     Instrumentation