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Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs

BACKGROUND: In the Mediterranean area, patients with LTP syndrome who are sensitized to multiple allergens are often tested for sIgE using multiplex platforms. The results obtained from different commercial platforms are not interchangeable, so it is important to compare and validate the platform se...

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Autores principales: Cabrera, Carmen Maria, Horrillo, Moisés Labrador, Brito, Francisco Feo, Palacios‐Cañas, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561593/
https://www.ncbi.nlm.nih.gov/pubmed/37638561
http://dx.doi.org/10.1002/jcla.24960
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author Cabrera, Carmen Maria
Horrillo, Moisés Labrador
Brito, Francisco Feo
Palacios‐Cañas, Alberto
author_facet Cabrera, Carmen Maria
Horrillo, Moisés Labrador
Brito, Francisco Feo
Palacios‐Cañas, Alberto
author_sort Cabrera, Carmen Maria
collection PubMed
description BACKGROUND: In the Mediterranean area, patients with LTP syndrome who are sensitized to multiple allergens are often tested for sIgE using multiplex platforms. The results obtained from different commercial platforms are not interchangeable, so it is important to compare and validate the platform selected for use. The objective of this study is to compare and validate the performance of the ImmunoCAP ISAC E112i and the macroarray ALEX2 in our daily practice. METHODS: From August 2021 to March 2022, we tested 20 random serum samples from polysensitized patients using the ALEX2 test (MADx) and ImmunoCAP tIgE and ISAC E112i (Thermo Fisher Scientific). We compared the total IgE (tIgE) and sIgE levels for shared allergens. RESULTS: The heatmap generally showed more intense results for ISAC. The overall correlation was good, but some exceptions were noted. The main discrepancies were found for Ole e 7, which was positive for 11 patients in ISAC but negative for all patients in ALEX2, and for nut LTPs, for which ISAC showed a threefold higher detection rate for Ara h 9 and a fivefold higher detection rate for Cor a 8 and Jug r 3 compared to ALEX2. The regression model showed no interchangeability of tIgE results. CONCLUSIONS: Despite our small sample size and the complexity of comparing a quantitative and a semi‐quantitative platform, our results suggest that patient diagnosis and management can be influenced by the platform used. Therefore, our findings must be taken into consideration when choosing a platform to use for some profiles of LTP‐polysensitized patients, even though more data is needed.
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spelling pubmed-105615932023-10-10 Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs Cabrera, Carmen Maria Horrillo, Moisés Labrador Brito, Francisco Feo Palacios‐Cañas, Alberto J Clin Lab Anal Brief Reports BACKGROUND: In the Mediterranean area, patients with LTP syndrome who are sensitized to multiple allergens are often tested for sIgE using multiplex platforms. The results obtained from different commercial platforms are not interchangeable, so it is important to compare and validate the platform selected for use. The objective of this study is to compare and validate the performance of the ImmunoCAP ISAC E112i and the macroarray ALEX2 in our daily practice. METHODS: From August 2021 to March 2022, we tested 20 random serum samples from polysensitized patients using the ALEX2 test (MADx) and ImmunoCAP tIgE and ISAC E112i (Thermo Fisher Scientific). We compared the total IgE (tIgE) and sIgE levels for shared allergens. RESULTS: The heatmap generally showed more intense results for ISAC. The overall correlation was good, but some exceptions were noted. The main discrepancies were found for Ole e 7, which was positive for 11 patients in ISAC but negative for all patients in ALEX2, and for nut LTPs, for which ISAC showed a threefold higher detection rate for Ara h 9 and a fivefold higher detection rate for Cor a 8 and Jug r 3 compared to ALEX2. The regression model showed no interchangeability of tIgE results. CONCLUSIONS: Despite our small sample size and the complexity of comparing a quantitative and a semi‐quantitative platform, our results suggest that patient diagnosis and management can be influenced by the platform used. Therefore, our findings must be taken into consideration when choosing a platform to use for some profiles of LTP‐polysensitized patients, even though more data is needed. John Wiley and Sons Inc. 2023-08-28 /pmc/articles/PMC10561593/ /pubmed/37638561 http://dx.doi.org/10.1002/jcla.24960 Text en © 2023 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Reports
Cabrera, Carmen Maria
Horrillo, Moisés Labrador
Brito, Francisco Feo
Palacios‐Cañas, Alberto
Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title_full Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title_fullStr Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title_full_unstemmed Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title_short Would the choice of multiplex platform impact the management of the allergic patient? A first approach focusing on LTPs
title_sort would the choice of multiplex platform impact the management of the allergic patient? a first approach focusing on ltps
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561593/
https://www.ncbi.nlm.nih.gov/pubmed/37638561
http://dx.doi.org/10.1002/jcla.24960
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