Cargando…

T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis

INTRODUCTION: T-614 is a novel oral antirheumatic agent for the treatment of rheumatoid arthritis. Whether it has immunomodulatory or disease-modifying properties and its mechanism of action are largely undetermined. METHODS: Rats with collagen-induced arthritis (CIA) were treated with T-614 (5 and...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Fang, Lü, Liang-jing, Fu, Qiong, Dai, Min, Teng, Jia-lin, Fan, Wei, Chen, Shun-le, Ye, Ping, Shen, Nan, Huang, Xin-fang, Qian, Jie, Bao, Chun-de
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656239/
https://www.ncbi.nlm.nih.gov/pubmed/19019215
http://dx.doi.org/10.1186/ar2554
_version_ 1782165483850563584
author Du, Fang
Lü, Liang-jing
Fu, Qiong
Dai, Min
Teng, Jia-lin
Fan, Wei
Chen, Shun-le
Ye, Ping
Shen, Nan
Huang, Xin-fang
Qian, Jie
Bao, Chun-de
author_facet Du, Fang
Lü, Liang-jing
Fu, Qiong
Dai, Min
Teng, Jia-lin
Fan, Wei
Chen, Shun-le
Ye, Ping
Shen, Nan
Huang, Xin-fang
Qian, Jie
Bao, Chun-de
author_sort Du, Fang
collection PubMed
description INTRODUCTION: T-614 is a novel oral antirheumatic agent for the treatment of rheumatoid arthritis. Whether it has immunomodulatory or disease-modifying properties and its mechanism of action are largely undetermined. METHODS: Rats with collagen-induced arthritis (CIA) were treated with T-614 (5 and 20 mg/kg) daily. Animals receiving methotrexate (1 mg/kg every 3 days) and the nonsteroidal anti-inflammatory agent nimesulide (10 mg/kg per day) were used as controls. A combination therapy group was treated with both T-614(10 mg/kg per day) and methotrexate (1 mg/kg every 3 days). Hind paw swelling was evaluated and radiographic scores calculated. Serum cytokine levels were assessed by Bio-plex analysis. Quantitative PCR was used to evaluate expression of mRNA for interferon-γ, IL-4 and IL-17. Serum IL-17 and anti-type II collagen antibodies (total IgG, IgG(1), IgG(2a), IgG(2b )and IgM) were measured using ELISA. RESULTS: Oral T-614 inhibited paw swelling and offered significant protection against arthritis-induced cartilage and bone erosion, comparable to the effects of methotrexate. CIA rats treated with T-614 exhibited decreases in both mRNA expression of IL-17 in peripheral blood mononuclear cells and lymph node cells, and circulating IL-17 in a dose-dependent manner. T-614 also reduced serum levels of tumor necrosis factor-α, IL-1β and IL-6. A synergistic effect was observed for the combination of methotrexate and T-614. In addition, T-614 (20 mg/kg per day) depressed production of anti-type II collagen antibodies and differentially affected levels of IgG(2a )subclasses in vivo, whereas IgM level was decreased without any change in the IgG(1 )level. Together, the findings presented here indicate that the novel agent T-614 has disease-modifying effects against experimental arthritis, as opposed to nimesulide. CONCLUSIONS: Our data suggested that T-614 is an effective disease-modifying agent that can prevent bone/cartilage destruction and inflammation in in CIA rats. Combination with methotrexate markedly enhances the therapeutic effect of T-614.
format Text
id pubmed-2656239
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26562392009-03-17 T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis Du, Fang Lü, Liang-jing Fu, Qiong Dai, Min Teng, Jia-lin Fan, Wei Chen, Shun-le Ye, Ping Shen, Nan Huang, Xin-fang Qian, Jie Bao, Chun-de Arthritis Res Ther Research Article INTRODUCTION: T-614 is a novel oral antirheumatic agent for the treatment of rheumatoid arthritis. Whether it has immunomodulatory or disease-modifying properties and its mechanism of action are largely undetermined. METHODS: Rats with collagen-induced arthritis (CIA) were treated with T-614 (5 and 20 mg/kg) daily. Animals receiving methotrexate (1 mg/kg every 3 days) and the nonsteroidal anti-inflammatory agent nimesulide (10 mg/kg per day) were used as controls. A combination therapy group was treated with both T-614(10 mg/kg per day) and methotrexate (1 mg/kg every 3 days). Hind paw swelling was evaluated and radiographic scores calculated. Serum cytokine levels were assessed by Bio-plex analysis. Quantitative PCR was used to evaluate expression of mRNA for interferon-γ, IL-4 and IL-17. Serum IL-17 and anti-type II collagen antibodies (total IgG, IgG(1), IgG(2a), IgG(2b )and IgM) were measured using ELISA. RESULTS: Oral T-614 inhibited paw swelling and offered significant protection against arthritis-induced cartilage and bone erosion, comparable to the effects of methotrexate. CIA rats treated with T-614 exhibited decreases in both mRNA expression of IL-17 in peripheral blood mononuclear cells and lymph node cells, and circulating IL-17 in a dose-dependent manner. T-614 also reduced serum levels of tumor necrosis factor-α, IL-1β and IL-6. A synergistic effect was observed for the combination of methotrexate and T-614. In addition, T-614 (20 mg/kg per day) depressed production of anti-type II collagen antibodies and differentially affected levels of IgG(2a )subclasses in vivo, whereas IgM level was decreased without any change in the IgG(1 )level. Together, the findings presented here indicate that the novel agent T-614 has disease-modifying effects against experimental arthritis, as opposed to nimesulide. CONCLUSIONS: Our data suggested that T-614 is an effective disease-modifying agent that can prevent bone/cartilage destruction and inflammation in in CIA rats. Combination with methotrexate markedly enhances the therapeutic effect of T-614. BioMed Central 2008 2008-11-19 /pmc/articles/PMC2656239/ /pubmed/19019215 http://dx.doi.org/10.1186/ar2554 Text en Copyright © 2008 Du et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Du, Fang
Lü, Liang-jing
Fu, Qiong
Dai, Min
Teng, Jia-lin
Fan, Wei
Chen, Shun-le
Ye, Ping
Shen, Nan
Huang, Xin-fang
Qian, Jie
Bao, Chun-de
T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title_full T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title_fullStr T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title_full_unstemmed T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title_short T-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
title_sort t-614, a novel immunomodulator, attenuates joint inflammation and articular damage in collagen-induced arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656239/
https://www.ncbi.nlm.nih.gov/pubmed/19019215
http://dx.doi.org/10.1186/ar2554
work_keys_str_mv AT dufang t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT luliangjing t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT fuqiong t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT daimin t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT tengjialin t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT fanwei t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT chenshunle t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT yeping t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT shennan t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT huangxinfang t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT qianjie t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis
AT baochunde t614anovelimmunomodulatorattenuatesjointinflammationandarticulardamageincollageninducedarthritis