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A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System

Many mouse models of rheumatoid arthritis have been identified, but only a limited number are present for axial spondyloarthritis (AxSpA). Collagen Ab-induced arthritis (CAIA) is one of the most widely used mouse models of arthritis, and it is complement-dependent. We found that mice developing CAIA...

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Autores principales: Holers, V. Michael, La Rosa, Francisco G., Banda, Nirmal K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733187/
https://www.ncbi.nlm.nih.gov/pubmed/35036032
http://dx.doi.org/10.4110/in.2021.21.e45
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author Holers, V. Michael
La Rosa, Francisco G.
Banda, Nirmal K.
author_facet Holers, V. Michael
La Rosa, Francisco G.
Banda, Nirmal K.
author_sort Holers, V. Michael
collection PubMed
description Many mouse models of rheumatoid arthritis have been identified, but only a limited number are present for axial spondyloarthritis (AxSpA). Collagen Ab-induced arthritis (CAIA) is one of the most widely used mouse models of arthritis, and it is complement-dependent. We found that mice developing CAIA also developed spinal lesions similar to those found in AxSpA. To induce CAIA, mice were injected intraperitoneally at day 0 with anti-collagen Abs, followed by LPS injection at day 3. CAIA mice demonstrated a significant kyphosis through the spine, as well as hypertrophic cartilage and osseous damage of the intravertebral joints. Immunohistochemical staining of the kyphotic area revealed increased complement C3 deposition and macrophage infiltration, with localization to the intravertebral joint margins. Near Infrared (NIR) in vivo imaging showed that anti-collagen Abs conjugated with IRDye(®) 800CW not only localized to cartilage surface in the joints but also to the spine in arthritic mice. We report here a novel preclinical mouse model in which, associated with the induction of CAIA, mice also exhibited salient features of AxSpA; this new experimental model of AxSpA may allow investigators to shed light on the local causal mechanisms of AxSpA bone and soft tissue changes as well as treatment.
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spelling pubmed-87331872022-01-14 A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System Holers, V. Michael La Rosa, Francisco G. Banda, Nirmal K. Immune Netw Brief Communication Many mouse models of rheumatoid arthritis have been identified, but only a limited number are present for axial spondyloarthritis (AxSpA). Collagen Ab-induced arthritis (CAIA) is one of the most widely used mouse models of arthritis, and it is complement-dependent. We found that mice developing CAIA also developed spinal lesions similar to those found in AxSpA. To induce CAIA, mice were injected intraperitoneally at day 0 with anti-collagen Abs, followed by LPS injection at day 3. CAIA mice demonstrated a significant kyphosis through the spine, as well as hypertrophic cartilage and osseous damage of the intravertebral joints. Immunohistochemical staining of the kyphotic area revealed increased complement C3 deposition and macrophage infiltration, with localization to the intravertebral joint margins. Near Infrared (NIR) in vivo imaging showed that anti-collagen Abs conjugated with IRDye(®) 800CW not only localized to cartilage surface in the joints but also to the spine in arthritic mice. We report here a novel preclinical mouse model in which, associated with the induction of CAIA, mice also exhibited salient features of AxSpA; this new experimental model of AxSpA may allow investigators to shed light on the local causal mechanisms of AxSpA bone and soft tissue changes as well as treatment. The Korean Association of Immunologists 2021-12-15 /pmc/articles/PMC8733187/ /pubmed/35036032 http://dx.doi.org/10.4110/in.2021.21.e45 Text en Copyright © 2021. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Holers, V. Michael
La Rosa, Francisco G.
Banda, Nirmal K.
A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title_full A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title_fullStr A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title_full_unstemmed A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title_short A Potential New Mouse Model of Axial Spondyloarthritis Involving the Complement System
title_sort potential new mouse model of axial spondyloarthritis involving the complement system
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733187/
https://www.ncbi.nlm.nih.gov/pubmed/35036032
http://dx.doi.org/10.4110/in.2021.21.e45
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