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

Author:

Cabrera Carmen Maria12ORCID,Horrillo Moisés Labrador34,Brito Francisco Feo5,Palacios‐Cañas Alberto5

Affiliation:

1. Allergy and Immunology Section Ciudad Real University General Hospital Ciudad Real Spain

2. Faculty of Medicine of Ciudad Real University of Castilla‐La Mancha Ciudad Real Spain

3. Allergy Section Vall d'Hebron University Hospital Barcelona Spain

4. Autonomous University of Barcelona Barcelona Spain

5. Allergy Section Ciudad Real University General Hospital Ciudad Real Spain

Abstract

AbstractBackgroundIn 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.MethodsFrom 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.ResultsThe 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.ConclusionsDespite 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.

Funder

Thermo Fisher Scientific

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

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