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Prediction of natalizumab anti-drug antibodies persistency.

Authors :
Deisenhammer, Florian
Jank, Marlies
Lauren, Anna
Sjödin, Anders
Ryner, Malin
Fogdell-Hahn, Anna
Sievers, Claudia
Lindberg, Raija
Jensen, Poul Erik
Sellebjerg, Finn
Christodoulou, Louis
Birchler, Mary
Pallardy, Marc
Auer, Michael
Liblau, Roland
Source :
Multiple Sclerosis Journal; Mar2019, Vol. 25 Issue 3, p392-398, 7p, 1 Chart, 3 Graphs
Publication Year :
2019

Abstract

Background: Anti-drug antibodies (ADA) against natalizumab develop early during treatment. ADA persistency is defined by two consecutive positive results as performed by the current qualitative ELISA assay (positive/negative). Very little is known about the magnitude of the natalizumab ADA response and persistency. Design/methods: We developed a highly sensitive natalizumab ADA titration assay on the Meso Scale Discovery (MSD) platform and a pharmacokinetic (PK) assay. We included 43 patients with a positive ELISA-ADA result within 6 months of treatment initiation (baseline) of whom a follow-up serum sample was available 12–30 months after treatment start. MSD-ADA titres and drug levels were measured. Results: Median MSD-ADA titre at baseline was 4881 and 303 at follow-up. A titre of >400 at baseline had a 94% sensitivity and 89% specificity to predict ADA persistency. Reversion to ADA negativity occurred in 10 patients with mean drug levels of 10.8 μg/mL. The median trough drug level in ADA-positive samples was 0 µg/mL. PK levels and ADA titres correlated strongly negatively (r = −0.67). Conclusion: High baseline natalizumab ADA titres accurately predict persistency. Despite continuous treatment, the majority of patients with persistent ADA had no detectable drug levels indicating loss of efficacy in line with phase 3 study results. [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
IMMUNOGLOBULINS
NATALIZUMAB

Details

Language :
English
ISSN :
13524585
Volume :
25
Issue :
3
Database :
Complementary Index
Journal :
Multiple Sclerosis Journal
Publication Type :
Academic Journal
Accession number :
135266355
Full Text :
https://doi.org/10.1177/1352458517753721