AI Article Synopsis

  • The study aimed to automate immunoassays for measuring serum levels of infliximab and adalimumab along with anti-drug antibodies using the CHORUS Promonitor kits.
  • By comparing the automated kits against the manual versions, researchers analyzed sensitivity and specificity while running tests using human serum samples and drug additions on the CHORUS TRIO instrument.
  • Results showed that the automated kits were highly accurate and consistent, demonstrating strong agreement with manual kits and confirming their potential for use in clinical settings for monitoring patients treated with these drugs.

Article Abstract

Objective: To convert manual ELISA kits to fully automated immunoassays that quantify serum drug levels and anti-drug antibodies levels of infliximab and adalimumab (CHORUS Promonitor kits).

Desing And Methods: CHORUS Promonitor INFLIXIMAB, CHORUS Promonitor ADALIMUMAB, CHORUS Promonitor ANTI-INFLIXIMAB, and CHORUS Promonitor ANTI-ADALIMUMAB kits were compared with the corresponding Promonitor kits to determine sensitivity and specificity of the assays. For the automated assays, the entire procedure -from samples dilution to final readouts-was performed by CHORUS TRIO instrument (DIESSE, Italy). Residual human serum samples from clinical laboratory investigations and samples resulting from the addition of specific drugs (IFX or ADL) or anti-drug antibodies (anti-IFX or anti-ADL) were used for the characterization and validation of the tests.

Results: CHORUS Promonitor kits showed an excellent agreement (Cohen's coefficient = 1) with the Promonitor kits and were linear within predefined ranges. All assays were accurate and repeatable, as an acceptable variability were observed within runs, between runs, lots, and instruments. No difference in detecting the reference drug or biosimilars emerged.

Conclusion: During preclinical development, these kits resulted as sensitive, specific, accurate, and able to quantify either the reference drug or the corresponding biosimilars. All these features support their use in clinical practice for therapeutic drug monitoring of patients with inflammatory diseases under treatment with IFX or ADL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10924048PMC
http://dx.doi.org/10.1016/j.plabm.2024.e00374DOI Listing

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