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Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis

INTRODUCTION: Angiogenesis is an important factor in the development of osteoarthritis (OA). We investigated the efficacy of bevacizumab, an antibody against vascular endothelial growth factor and an inhibitor of angiogenesis, in the treatment of OA using a rabbit model of anterior cruciate ligament...

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Autores principales: Nagai, Toshihiro, Sato, Masato, Kobayashi, Miyuki, Yokoyama, Munetaka, Tani, Yoshiki, Mochida, Joji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189677/
https://www.ncbi.nlm.nih.gov/pubmed/25230745
http://dx.doi.org/10.1186/s13075-014-0427-y
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author Nagai, Toshihiro
Sato, Masato
Kobayashi, Miyuki
Yokoyama, Munetaka
Tani, Yoshiki
Mochida, Joji
author_facet Nagai, Toshihiro
Sato, Masato
Kobayashi, Miyuki
Yokoyama, Munetaka
Tani, Yoshiki
Mochida, Joji
author_sort Nagai, Toshihiro
collection PubMed
description INTRODUCTION: Angiogenesis is an important factor in the development of osteoarthritis (OA). We investigated the efficacy of bevacizumab, an antibody against vascular endothelial growth factor and an inhibitor of angiogenesis, in the treatment of OA using a rabbit model of anterior cruciate ligament transection. METHODS: First, we evaluated the response of gene expression and histology of the normal joint to bevacizumab treatment. Next, in a rabbit model of OA induced by anterior cruciate ligament transection, we used macroscopic and histological evaluations and real-time polymerase chain reaction (PCR) to examine the responses to intravenous (systemic) administration of bevacizumab (OAB IV group). We also investigated the efficacy of intra-articular (local) administration of bevacizumab in OA-induced rabbits (OAB IA group). RESULTS: Histologically, bevacizumab had no negative effect in normal joints. Bevacizumab did not increase the expression of genes for catabolic factors in the synovium, subchondral bone, or articular cartilage, but it increased the expression of collagen type 2 in the articular cartilage. Macroscopically and histologically, the OAB IV group exhibited a reduction in articular cartilage degeneration and less osteophyte formation and synovitis compared with the control group (no bevacizumab; OA group). Real-time PCR showed significantly lower expression of catabolic factors in the synovium in the OAB IV group compared with the OA group. In articular cartilage, expression levels of aggrecan, collagen type 2, and chondromodulin-1 were higher in the OAB IV group than in the OA group. Histological evaluation and assessment of pain behaviour showed a superior effect in the OAB IA group compared with the OAB IV group 12 weeks after administration of bevacizumab, even though the total dosage given to the OAB IA group was half that received by the OAB IV group. CONCLUSIONS: Considering the dosage and potential adverse effects of bevacizumab, the local administration of bevacizumab is a more advantageous approach than systemic administration. Our results suggest that intra-articular bevacizumab may offer a new therapeutic approach for patients with post-traumatic OA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0427-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-41896772014-10-23 Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis Nagai, Toshihiro Sato, Masato Kobayashi, Miyuki Yokoyama, Munetaka Tani, Yoshiki Mochida, Joji Arthritis Res Ther Research Article INTRODUCTION: Angiogenesis is an important factor in the development of osteoarthritis (OA). We investigated the efficacy of bevacizumab, an antibody against vascular endothelial growth factor and an inhibitor of angiogenesis, in the treatment of OA using a rabbit model of anterior cruciate ligament transection. METHODS: First, we evaluated the response of gene expression and histology of the normal joint to bevacizumab treatment. Next, in a rabbit model of OA induced by anterior cruciate ligament transection, we used macroscopic and histological evaluations and real-time polymerase chain reaction (PCR) to examine the responses to intravenous (systemic) administration of bevacizumab (OAB IV group). We also investigated the efficacy of intra-articular (local) administration of bevacizumab in OA-induced rabbits (OAB IA group). RESULTS: Histologically, bevacizumab had no negative effect in normal joints. Bevacizumab did not increase the expression of genes for catabolic factors in the synovium, subchondral bone, or articular cartilage, but it increased the expression of collagen type 2 in the articular cartilage. Macroscopically and histologically, the OAB IV group exhibited a reduction in articular cartilage degeneration and less osteophyte formation and synovitis compared with the control group (no bevacizumab; OA group). Real-time PCR showed significantly lower expression of catabolic factors in the synovium in the OAB IV group compared with the OA group. In articular cartilage, expression levels of aggrecan, collagen type 2, and chondromodulin-1 were higher in the OAB IV group than in the OA group. Histological evaluation and assessment of pain behaviour showed a superior effect in the OAB IA group compared with the OAB IV group 12 weeks after administration of bevacizumab, even though the total dosage given to the OAB IA group was half that received by the OAB IV group. CONCLUSIONS: Considering the dosage and potential adverse effects of bevacizumab, the local administration of bevacizumab is a more advantageous approach than systemic administration. Our results suggest that intra-articular bevacizumab may offer a new therapeutic approach for patients with post-traumatic OA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0427-y) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-18 2014 /pmc/articles/PMC4189677/ /pubmed/25230745 http://dx.doi.org/10.1186/s13075-014-0427-y Text en © Nagai et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Nagai, Toshihiro
Sato, Masato
Kobayashi, Miyuki
Yokoyama, Munetaka
Tani, Yoshiki
Mochida, Joji
Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title_full Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title_fullStr Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title_full_unstemmed Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title_short Bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
title_sort bevacizumab, an anti-vascular endothelial growth factor antibody, inhibits osteoarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189677/
https://www.ncbi.nlm.nih.gov/pubmed/25230745
http://dx.doi.org/10.1186/s13075-014-0427-y
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