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Canine IL4-10 fusion protein provides disease modifying activity in a canine model of OA; an exploratory study.

Authors :
van Helvoort EM
Popov-Celeketic J
Eijkelkamp N
Coeleveld K
Tryfonidou MA
Wijne CD
Hack CE
Lafeber FPJG
Mastbergen SC
Source :
PloS one [PLoS One] 2019 Jul 11; Vol. 14 (7), pp. e0219587. Date of Electronic Publication: 2019 Jul 11 (Print Publication: 2019).
Publication Year :
2019

Abstract

Objective: An ideal disease modifying osteoarthritis drug (DMOAD) has chondroprotective, anti-inflammatory, and analgesic effects. This study describes the production and characterization of a canine IL4-10 fusion protein (IL4-10 FP) and evaluates its in vivo DMOAD activity in a canine model of osteoarthritis (OA).<br />Design: The canine Groove model was used as an in vivo model of degenerative knee OA. Six weeks after OA induction dogs were intra-articularly injected weekly, for ten weeks, with either IL4-10 FP or phosphate buffered saline (PBS). In addition to the use of human IL4-10 FP, canine IL4-10 FP was developed and characterized in vitro, and tested in vivo. Force plate analysis (FPA) was performed to analyze joint loading as a proxy measure for pain. After ten weeks dogs were euthanized and cartilage and synovial tissue samples were analyzed by histochemistry (OARSI scores) and biochemistry (cartilage proteoglycan turnover).<br />Results: Repetitive intra-articular injections with human IL4-10 FP led to antibody formation, that blocked its functional activity. Therefore, a canine IL4-10 FP was developed, which completely inhibited LPS-induced TNFα production by canine blood cells, and increased proteoglycan synthesis of canine cartilage in vitro (p = 0.043). In vivo, canine IL4-10 FP restored the, by OA impaired, joint loading (p = 0.002) and increased cartilage proteoglycan content (p = 0.029).<br />Conclusions: This first study on the potential DMOAD activity upon prolonged repeated treatment with IL4-10 FP demonstrates that a species-specific variant has anti-inflammatory and chondroprotective effects in vitro and chondroprotective and analgesic effects in vivo. These data warrant further research on the DMOAD potential of the IL4-10 FP.<br />Competing Interests: FL and CEH are inventors on the patent WO2013070076 owned by UMC Utrecht Holdings. This does not alter our adherence to PLOS ONE policies on sharing data and materials. JP, NE, and CEH are shareholders of Synerkine Pharma BV, a spin-off of the UMC Utrecht licensing the patents on the IL4-10 fusion protein.

Details

Language :
English
ISSN :
1932-6203
Volume :
14
Issue :
7
Database :
MEDLINE
Journal :
PloS one
Publication Type :
Academic Journal
Accession number :
31295306
Full Text :
https://doi.org/10.1371/journal.pone.0219587