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

J Clin Lab Anal. 2023 Aug;37(15-16):e24960. doi: 10.1002/jcla.24960. Epub 2023 Aug 28.

Abstract

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.

Keywords: ALEX2; ISAC; LTP; clinical impact; comparison.

MeSH terms

  • Allergens
  • Arabinonucleosides
  • Humans
  • Hypersensitivity* / diagnosis
  • Immunoglobulin E*

Substances

  • Immunoglobulin E
  • Allergens
  • Arabinonucleosides

Grants and funding