类风湿性关节炎
不利影响
血管翳
医学
滑膜炎
药品
疾病
依那西普
重症监护医学
托珠单抗
免疫系统
免疫学
生物信息学
药理学
内科学
生物
作者
Manoj Khokhar,Sharmistha Dey,Sojit Tomo,Mariusz Jaremko,Abdul‐Hamid Emwas,Rajan Kumar Pandey
出处
期刊:ACS pharmacology & translational science
[American Chemical Society]
日期:2024-05-28
卷期号:7 (6): 1664-1693
标识
DOI:10.1021/acsptsci.4c00067
摘要
Rheumatoid arthritis (RA) is a chronic debilitating autoimmune disease, that causes joint damage, deformities, and decreased functionality. In addition, RA can also impact organs like the skin, lungs, eyes, and blood vessels. This autoimmune condition arises when the immune system erroneously targets the joint synovial membrane, resulting in synovitis, pannus formation, and cartilage damage. RA treatment is often holistic, integrating medication, physical therapy, and lifestyle modifications. Its main objective is to achieve remission or low disease activity by utilizing a "treat-to-target" approach that optimizes drug usage and dose adjustments based on clinical response and disease activity markers. The primary RA treatment uses disease-modifying antirheumatic drugs (DMARDs) that help to interrupt the inflammatory process. When there is an inadequate response, a combination of biologicals and DMARDs is recommended. Biological therapies target inflammatory pathways and have shown promising results in managing RA symptoms. Close monitoring for adverse effects and disease progression is critical to ensure optimal treatment outcomes. A deeper understanding of the pathways and mechanisms will allow new treatment strategies that minimize adverse effects and maintain quality of life. This review discusses the potential targets that can be used for designing and implementing precision medicine in RA treatment, spotlighting the latest breakthroughs in biologics, JAK inhibitors, IL-6 receptor antagonists, TNF blockers, and disease-modifying noncoding RNAs.
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