Validating the positivity thresholds of drug‐tolerant anti‐infliximab and anti‐adalimumab antibody assays

Author:

Nice Rachel1,Chanchlani Neil23ORCID,Green Harry3ORCID,Bewshea Claire3ORCID,Ahmad Tariq23ORCID,Goodhand James R.23ORCID,McDonald Timothy J.1ORCID,Perry Mandy H.1,Kennedy Nicholas A.23ORCID

Affiliation:

1. Department of Blood Science Royal Devon and Exeter Hospital NHS Foundation Trust Exeter UK

2. Department of Gastroenterology Royal Devon and Exeter Hospital NHS Foundation Trust Exeter UK

3. Exeter IBD Pharmacogenetics Research Group University of Exeter Exeter UK

Abstract

SummaryBackgroundWhen used proactively, drug‐tolerant anti‐tumour necrosis factor (TNF) antibody assays provide early opportunity to suppress immunogenicity.AimTo validate positivity thresholds of IDKmonitor drug‐tolerant anti‐infliximab and ‐adalimumab antibody assays.MethodsWe applied positivity thresholds, defined by testing sera from 498 anti‐TNF naive healthy adults, from the Exeter Ten Thousand study to data from our therapeutic drug monitoring (TDM) service and Personalised Anti‐TNF Therapy in Crohn's disease (PANTS) cohort to explore associations with drug level and treatment outcomes.ResultsThe 80% one‐sided lower confidence interval of the 99th centile concentration for anti‐infliximab and –adalimumab antibodies were lower than the manufacturers threshold of 10 arbitrary units (AU)/mL; 9 and 6 AU/mL, respectively. Using these new thresholds in the TDM cohort, more adalimumab‐ than infliximab‐ (11.2% [814/7272] vs 3.1% [390/12 683] P < 0.0001) treated patients were reclassified as antibody‐positive. Adalimumab drug concentrations in this reclassified group (median 8.1, interquartile range [IQR] 5.5‐11.0 mg/L) were lower than those below the new threshold (<5AU/mL) (median 9.9, IQR 7.1‐13.0 mg/L; P < 0.0001), but higher than at the manufacturer's threshold (10‐29 AU/mL) (median 5.9 mg/L, IQR 3.5‐8.7; P < 0.0001). No difference in infliximab drug concentration was observed using the new or manufacturer's positivity threshold (P = 0.11). In the PANTS cohort, patients with anti‐adalimumab antibody concentrations at or above the new threshold were more likely to be in primary non‐response (25/68 [37%] vs. 64/332 [19%], P = 0.0035), and non‐remission at week 54 (51/62 [82%] vs. 168/279 [60%], P = 0.0011), than patients with anti‐drug antibody concentrations in the group below the new threshold (0‐5 AU/mL); this was not seen for anti‐infliximab antibodies.ConclusionLaboratories should derive antibody positivity thresholds for assays they use. For adalimumab, low‐concentration anti‐drug antibodies were associated with lower drug levels and treatment failure.

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

Reference42 articles.

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2. Influence of Immunogenicity on the Long-Term Efficacy of Infliximab in Crohn's Disease

3. Predictors of anti‐TNF treatment failure in anti‐TNF‐naive patients with active luminal Crohn’s disease: a prospective, multicentre, cohort study;Kennedy NA;Lancet Gastroenterol Hepatol,2019

4. Immunogenicity of biologics in inflammatory bowel disease

5. Influence of Trough Serum Levels and Immunogenicity on Long-term Outcome of Adalimumab Therapy in Crohn's Disease

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