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Validation of a Multiplex Assay for Measuring Specific IgG4
PURPOSE: Specific IgG4 (sIgG4) increases with allergen specific immunotherapy and may reflect a state of immune tolerance in food allergy. While ImmunoCAP® has been widely used to measure sIgG4 to a single allergen, PROTIA™ Specific IgG4® has been designed as a multiplex assay for measuring sIgG4. T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255997/ https://www.ncbi.nlm.nih.gov/pubmed/32469176 http://dx.doi.org/10.3349/ymj.2020.61.6.524 |
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author | Kim, Sung-Ryeol Park, Kyung Hee Lee, Ji Eun Kim, Bum Joon Lim, Kook Jin Park, Jung-Won |
author_facet | Kim, Sung-Ryeol Park, Kyung Hee Lee, Ji Eun Kim, Bum Joon Lim, Kook Jin Park, Jung-Won |
author_sort | Kim, Sung-Ryeol |
collection | PubMed |
description | PURPOSE: Specific IgG4 (sIgG4) increases with allergen specific immunotherapy and may reflect a state of immune tolerance in food allergy. While ImmunoCAP® has been widely used to measure sIgG4 to a single allergen, PROTIA™ Specific IgG4® has been designed as a multiplex assay for measuring sIgG4. This study sought to validate this assay in comparison to ImmunoCAP®. MATERIALS AND METHODS: Measurements of sIgG4 were compared between PROTIA™ Specific IgG4® and ImmunoCAP® using sera from 519 allergy patients (asthma: 114, allergic rhinitis: 318, food allergy: 146) with 731 paired tests. sIgG4 was measured against nine inhalant allergens (Dermatophagoides pteronyssinus, Dermatophagoides farinae, cat dander, dog dander, birch pollen, oak pollen, ragweed pollen, mugwort pollen, and Alternaria alternata spores) and nine food allergens (egg white, casein, wheat, peanut, walnut, crab, shrimp, apple, and peach). RESULTS: PROTIA™ Specific IgG4® showed 95.6% agreement rate with ImmunoCAP® in the positivity comparison. For sIgG4 positivity to each individual allergen, an agreement rate of more than 84.8% was observed. In Cohen's kappa analysis, these assays displayed substantial correlations [Cohen's kappa coefficient (κ) ≥0.699], except for shrimp (κ=0.448). Furthermore, both assays displayed strong correlations in quantitative comparisons [correlation coefficients value (ρ) ≥0.8014], except for apple (ρ=0.6571, p=0.175). Serial dilution tests also showed consistency between the assays. CONCLUSION: PROTIA™ Specific IgG4® showed high consistency with ImmunoCAP® in measuring sIgG4. This assay is applicable to various clinical fields, including allergen immunotherapy and food allergy. |
format | Online Article Text |
id | pubmed-7255997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-72559972020-06-08 Validation of a Multiplex Assay for Measuring Specific IgG4 Kim, Sung-Ryeol Park, Kyung Hee Lee, Ji Eun Kim, Bum Joon Lim, Kook Jin Park, Jung-Won Yonsei Med J Original Article PURPOSE: Specific IgG4 (sIgG4) increases with allergen specific immunotherapy and may reflect a state of immune tolerance in food allergy. While ImmunoCAP® has been widely used to measure sIgG4 to a single allergen, PROTIA™ Specific IgG4® has been designed as a multiplex assay for measuring sIgG4. This study sought to validate this assay in comparison to ImmunoCAP®. MATERIALS AND METHODS: Measurements of sIgG4 were compared between PROTIA™ Specific IgG4® and ImmunoCAP® using sera from 519 allergy patients (asthma: 114, allergic rhinitis: 318, food allergy: 146) with 731 paired tests. sIgG4 was measured against nine inhalant allergens (Dermatophagoides pteronyssinus, Dermatophagoides farinae, cat dander, dog dander, birch pollen, oak pollen, ragweed pollen, mugwort pollen, and Alternaria alternata spores) and nine food allergens (egg white, casein, wheat, peanut, walnut, crab, shrimp, apple, and peach). RESULTS: PROTIA™ Specific IgG4® showed 95.6% agreement rate with ImmunoCAP® in the positivity comparison. For sIgG4 positivity to each individual allergen, an agreement rate of more than 84.8% was observed. In Cohen's kappa analysis, these assays displayed substantial correlations [Cohen's kappa coefficient (κ) ≥0.699], except for shrimp (κ=0.448). Furthermore, both assays displayed strong correlations in quantitative comparisons [correlation coefficients value (ρ) ≥0.8014], except for apple (ρ=0.6571, p=0.175). Serial dilution tests also showed consistency between the assays. CONCLUSION: PROTIA™ Specific IgG4® showed high consistency with ImmunoCAP® in measuring sIgG4. This assay is applicable to various clinical fields, including allergen immunotherapy and food allergy. Yonsei University College of Medicine 2020-06-01 2020-05-25 /pmc/articles/PMC7255997/ /pubmed/32469176 http://dx.doi.org/10.3349/ymj.2020.61.6.524 Text en © Copyright: Yonsei University College of Medicine 2020 https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Sung-Ryeol Park, Kyung Hee Lee, Ji Eun Kim, Bum Joon Lim, Kook Jin Park, Jung-Won Validation of a Multiplex Assay for Measuring Specific IgG4 |
title | Validation of a Multiplex Assay for Measuring Specific IgG4 |
title_full | Validation of a Multiplex Assay for Measuring Specific IgG4 |
title_fullStr | Validation of a Multiplex Assay for Measuring Specific IgG4 |
title_full_unstemmed | Validation of a Multiplex Assay for Measuring Specific IgG4 |
title_short | Validation of a Multiplex Assay for Measuring Specific IgG4 |
title_sort | validation of a multiplex assay for measuring specific igg4 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255997/ https://www.ncbi.nlm.nih.gov/pubmed/32469176 http://dx.doi.org/10.3349/ymj.2020.61.6.524 |
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