An alternative inhibition method for determining cross-reactive allergens
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Yvonne Schmidt-Hieltjes
Abstract
Background:
Inhibition assays are an useful tool to identify the allergen of primary sensitization of cross-reactive allergens. Classical ELISA-based inhibition assays are limited by both the availability of commercial standardized allergen extracts and the experience and knowledge needed for making home-made extracts. Moreover the direct comparison of the inhibition ELISAs outcomes between different laboratories is difficult because of different sources of used allergen extracts and a number of methodological variations. Therefore, we propose a novel ImmunoCap (Phadia, Thermofisher Scientific) based immunoinhibition method with the use of commercially available Caps as the allergen source.
Methods:
The novel ImmunoCap based immunoinhibition method was developed and tested with sera from patients with a well-known cross-reactive sensitization for fig (Ficus carica) and ficus (Ficus benjamina). Results were compared with a classically applied inhibition method, i.e. addition of homemade allergen extract to patient serum.
Results:
The amount of allergens (fig and ficus extracts) needed to reach a similar degree of inhibition was comparable for both inhibition methods.
Conclusions:
The ImmunoCap based inhibition assay, in addition to classical inhibition methods, is a valuable tool as the ImmunoCap analyzer and commercial allergens (Caps) are more widely available which makes the outcomes of inhibition tests comparable between different laboratories. Furthermore, in the ImmunoCap inhibition method the same protein source is used for both the inhibition of sIgE and sIgE measurement, which might be even more relevant when multiple cross-reactive allergens are tested.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
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©2017 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorial
- Commutable samples with assigned target concentrations may help us harmonise general chemistry results
- Reviews
- Performance of point-of-care HbA1c test devices: implications for use in clinical practice – a systematic review and meta-analysis
- Cardiac troponins and mortality in type 1 and 2 myocardial infarction
- Opinion Paper
- Criteria for assigning laboratory measurands to models for analytical performance specifications defined in the 1st EFLM Strategic Conference
- Genetics and Molecular Diagnostics
- External quality assessment for human papillomavirus 16/18 DNA detection and genotyping in Shanghai, China
- General Clinical Chemistry and Laboratory Medicine
- Analytical performance of 17 general chemistry analytes across countries and across manufacturers in the INPUtS project of EQA organizers in Italy, the Netherlands, Portugal, United Kingdom and Spain
- Commutability of proficiency testing material containing tobramycin: a study within the framework of the Dutch Calibration 2.000 project
- Optimization and validation of moving average quality control procedures using bias detection curves and moving average validation charts
- Extending laboratory automation to the wards: effect of an innovative pneumatic tube system on diagnostic samples and transport time
- Smart management of sample dilution using an artificial neural network to achieve streamlined processes and saving resources: the automated nephelometric testing of serum free light chain as case study
- An integrated proteomic and peptidomic assessment of the normal human urinome
- An alternative inhibition method for determining cross-reactive allergens
- Validation of a new assay for α-synuclein detection in cerebrospinal fluid
- Reference Values and Biological Variations
- Intra-individual variation of plasma trimethylamine-N-oxide (TMAO), betaine and choline over 1 year
- Cancer Diagnostics
- Predictive performance of TPA testing for recurrent disease during follow-up after curative intent surgery for colorectal carcinoma
- Cardiovascular Diseases
- Mid-regional pro-adrenomedullin (MR-proADM) and mid-regional pro-atrial natriuretic peptide (MR-proANP) in severe aortic valve stenosis: association with outcome after transcatheter aortic valve implantation (TAVI)
- Association between apolipoprotein E polymorphisms and premature coronary artery disease: a meta-analysis
- Urinary orosomucoid: a novel, early biomarker of sepsis with promising diagnostic performance
- Letters to the Editor
- CT or MRI
- Reply to: CT or MRI in the diagnosis of right lower quadrant abdominal pain?
- Quantification of daratumumab in the serum protein electrophoresis
- Response to: Interference of daratumumab on the serum protein electrophoresis
- Glycated albumin: correlation to HbA1c and preliminary reference interval evaluation
- Using “big data” to describe the effect of seasonal variation in thyroid-stimulating hormone
- IgE multiple myeloma: a new case report
- Therapeutic decision-making process in the intensive care unit: role of biological point-of-care testing
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