Testing of monoclonal antibodies against the T-cell receptor associated with ankylosing spondylitis

Author:

Israelson MA1,Stepanov AV2,Staroverov DB3,Shagina IA4,Misorin AK5ORCID,Evstratieva AV5,Merzlyak EM3ORCID,Bogdanova EA4,Britanova OV6,Lukyanov SA7ORCID

Affiliation:

1. Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University, Moscow; Department of Adaptive Immunity Genomics, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia

2. Department of Peptide and Protein Technologies, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia

3. Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University, Moscow; Department of Adaptive Immunity Genomics, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Moscow

4. Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University, Moscow

5. BIOCAD, Saint-Petersburg

6. Department of Adaptive Immunity Genomics, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia

7. Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University, Moscow, Russia

Abstract

In the last decade there has been a tendency to move away from the symptomatic treatment and embrace targeted therapies. This process is underpinned by the accumulated knowledge of the mechanisms underlying the pathogenesis of diseases and driven by the advances in biotechnologies. T-cell receptors with variable TRBV9 β-chain regions have been recently associated with spondyloarthritis including its subtype, ankylosing spondylitis. The aim of this work was to engineer a chimeric monoclonal antibody targeting the variable region of the T-cell receptor β-chain encoded by the TRBV9 gene segment and assess its specificity and cytotoxicity. Using flow cytometry and next generation sequencing, we demonstrate that the engineered chimeric antibody is highly specific and exhibits cytotoxic activity against its target. Approaches based on the use of therapeutic chimeric antibodies against pathogenic T-clones may hold great promise for the therapy of autoimmune disorders in general and AS in particular.

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Pirogov Russian National Research Medical University

Subject

General Medicine

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