Cargando…
Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis
Rheumatoid arthritis (RA) is a chronic, inflammatory autoimmune disease of unknown etiology. It is characterized by the presence of rheumatoid factor and anticitrullinated peptide antibodies. The orchestra of the inflammatory process among various immune cells, cytokines, chemokines, proteases, matr...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470801/ https://www.ncbi.nlm.nih.gov/pubmed/30884802 http://dx.doi.org/10.3390/ijms20061332 |
_version_ | 1783411880347303936 |
---|---|
author | Chen, Shyi-Jou Lin, Gu-Jiun Chen, Jing-Wun Wang, Kai-Chen Tien, Chiung-Hsi Hu, Chih-Fen Chang, Chia-Ning Hsu, Wan-Fu Fan, Hueng-Chuen Sytwu, Huey-Kang |
author_facet | Chen, Shyi-Jou Lin, Gu-Jiun Chen, Jing-Wun Wang, Kai-Chen Tien, Chiung-Hsi Hu, Chih-Fen Chang, Chia-Ning Hsu, Wan-Fu Fan, Hueng-Chuen Sytwu, Huey-Kang |
author_sort | Chen, Shyi-Jou |
collection | PubMed |
description | Rheumatoid arthritis (RA) is a chronic, inflammatory autoimmune disease of unknown etiology. It is characterized by the presence of rheumatoid factor and anticitrullinated peptide antibodies. The orchestra of the inflammatory process among various immune cells, cytokines, chemokines, proteases, matrix metalloproteinases (MMPs), and reactive oxidative stress play critical immunopathologic roles in the inflammatory cascade of the joint environment, leading to clinical impairment and RA. With the growing understanding of the immunopathogenic mechanisms, increasingly novel marked and potential biologic agents have merged for the treatment of RA in recent years. In this review, we focus on the current understanding of pathogenic mechanisms, highlight novel biologic disease-modifying antirheumatic drugs (DMRADs), targeted synthetic DMRADs, and immune-modulating agents, and identify the applicable immune-mediated therapeutic strategies of the near future. In conclusion, new therapeutic approaches are emerging through a better understanding of the immunopathophysiology of RA, which is improving disease outcomes better than ever. |
format | Online Article Text |
id | pubmed-6470801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64708012019-04-26 Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis Chen, Shyi-Jou Lin, Gu-Jiun Chen, Jing-Wun Wang, Kai-Chen Tien, Chiung-Hsi Hu, Chih-Fen Chang, Chia-Ning Hsu, Wan-Fu Fan, Hueng-Chuen Sytwu, Huey-Kang Int J Mol Sci Review Rheumatoid arthritis (RA) is a chronic, inflammatory autoimmune disease of unknown etiology. It is characterized by the presence of rheumatoid factor and anticitrullinated peptide antibodies. The orchestra of the inflammatory process among various immune cells, cytokines, chemokines, proteases, matrix metalloproteinases (MMPs), and reactive oxidative stress play critical immunopathologic roles in the inflammatory cascade of the joint environment, leading to clinical impairment and RA. With the growing understanding of the immunopathogenic mechanisms, increasingly novel marked and potential biologic agents have merged for the treatment of RA in recent years. In this review, we focus on the current understanding of pathogenic mechanisms, highlight novel biologic disease-modifying antirheumatic drugs (DMRADs), targeted synthetic DMRADs, and immune-modulating agents, and identify the applicable immune-mediated therapeutic strategies of the near future. In conclusion, new therapeutic approaches are emerging through a better understanding of the immunopathophysiology of RA, which is improving disease outcomes better than ever. MDPI 2019-03-16 /pmc/articles/PMC6470801/ /pubmed/30884802 http://dx.doi.org/10.3390/ijms20061332 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chen, Shyi-Jou Lin, Gu-Jiun Chen, Jing-Wun Wang, Kai-Chen Tien, Chiung-Hsi Hu, Chih-Fen Chang, Chia-Ning Hsu, Wan-Fu Fan, Hueng-Chuen Sytwu, Huey-Kang Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title | Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title_full | Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title_fullStr | Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title_full_unstemmed | Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title_short | Immunopathogenic Mechanisms and Novel Immune-Modulated Therapies in Rheumatoid Arthritis |
title_sort | immunopathogenic mechanisms and novel immune-modulated therapies in rheumatoid arthritis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470801/ https://www.ncbi.nlm.nih.gov/pubmed/30884802 http://dx.doi.org/10.3390/ijms20061332 |
work_keys_str_mv | AT chenshyijou immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT lingujiun immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT chenjingwun immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT wangkaichen immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT tienchiunghsi immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT huchihfen immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT changchianing immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT hsuwanfu immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT fanhuengchuen immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis AT sytwuhueykang immunopathogenicmechanismsandnovelimmunemodulatedtherapiesinrheumatoidarthritis |