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  Anti-CCD absorbent

  Clinical

  Anti-CCD absorbent is an additional reagent designed for the incubation with blot-based allergy profiles. The absorbent eliminates anti-CCD IgE antibodies from patient serum, which increases the specificity of test results if these antibodies are present in the sample.

  Anti-CCD IgE antibodies are directed against sugar structures of proteins and can be detected in around 25 % of allergy patients as well as in non-allergic individuals. They generally have no clinical relevance.

  In extract-based in vitro allergy diagnostics, these antibodies complicate the interpretation of positive results because the following cases cannot be differentiated:

  • positive reaction caused by IgE antibodies against peptide epitopes
  • positive reaction caused by anti-CCD IgE antibodies
  • positive reaction caused by a combination of the two antibody types

  Differentiation between the described reactions is possible if the absorbent is used and the anti-CCD IgE antibodies are eliminated.

  The anti-CCD absorbent is useful if the patient sample demonstrably contains IgE antibodies against CCD structures. This is indicated by a positive CCD band on the incubated allergy profile. In this case, the serum should be retested using the anti-CCD absorbent.

  Diagnostics

  The patient sample is incubated with anti-CCD absorbent for 60 minutes at room temperature according to the instruction provided with the reagent. The sample can then be used directly in the incubation with the respective allergy profile.

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  Inhalation

  Clinical information

  With the inhalation allergies, the allergens enter the body via the air the mucous membranes and lead to measurable IgE concentration.  Seasonal allergen source (pollen from trees, grasses and herbs) play a role, as do also indoor allergens (house dust mites, domestic animals and mould spores) which occur the whole year round. The symptoms usually occur shortly after contact with the allergen. This is referred to as immediate type reaction and affects more than 15% of the population in the industrialised countries. Typical allergic reactions are rhinitis, conjunctivitis and allergic asthma. In rare cases, systemic allergic reactions may occur which are associated with severe, sometimes life-threatening symptoms (anaphylactic shock).

  Diagnostics

  For clarification of sensitisation to inhalation allergens, EUROIMMUN offers different inhalation profiles (EUROLINE). These permit the in vitro determination of human IgE antibodies against the most frequent inhalation allergens in serum or plasma. Moreover, country-specific inhalation profiles are available which vary in their allergen composition and are optimised with regard to the regional conditions.

  Moreover, the Total IgE ELISA can determine the total IgE concentration, allowing differentiation between allergic and intrinsic asthma, between rhinitis allergica and vasomotorica and between atopical and seborrhoic dermatitis.

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  Atopy

  Clinical information

  The term atopy describes the innate tendency to allergic hypersensitivity reactions which may present with different clinical images. The allergens responsible for the reaction enter the body either through the air and the mucous membranes (in the case of inhalation allergies), or through food ingestion (in the case of food allergies).

  Diagnostics

  For clarification of multiple sensitisations, EUROIMMUN offers different atopy profiles (EUROLINE). These permit the simultaneous in vitro determination of different human IgE antibodies against the most frequent inhalation and food allergens in serum or plasma. Moreover, country-specific profiles are available which take into account the characteristics of the regional allergen exposure.

  In addition, the total IgE concentration can be determined using the Total IgE ELISA.

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