Abstract
Drugs formulated from monoclonal antibodies (mAbs) are clinically effective in various diseases. Repeated administration of mAbs, however, elicits an immune response in the form of anti-drug-antibodies (ADA), thereby reducing the drug's efficacy. Notwithstanding their importance, the molecular landscape of ADA and the mechanisms involved in their formation are not fully understood. Using a newly developed quantitative bio-immunoassay, we found that ADA concentrations specific to TNFα antagonists can exceed extreme concentrations of 1 mg/ml with a wide range of neutralization capacity. Our data further suggest a preferential use of the λ light chain in a subset of neutralizing ADA. Moreover, we show that administration of TNFα antagonists result in a vaccine-like response whereby ADA formation is governed by the extrafollicular T cell-independent immune response. Our bio-immunoassay coupled with insights on the nature of the immune response can be leveraged to improve mAb immunogenicity assessment and facilitate improvement in therapeutic intervention strategies.
Original language | English |
---|---|
Article number | 2921 |
Journal | Frontiers in Immunology |
Volume | 10 |
DOIs | |
State | Published - 18 Dec 2019 |
Keywords
- anti-drug antibodies
- antibody repertoire
- biologics
- high-throughput sequencing
- immunogenicity
- monoclonal antibody
- next generation sequencing
- proteomics
All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Immunology