Therapeutic Utility and Adverse Effects of Biologic Disease-Modifying Anti-Rheumatic Drugs in Inflammatory Arthritis.
Hong-Ki MinSe Hee KimHae-Rim KimSang-Heon LeePublished in: International journal of molecular sciences (2022)
Targeting specific pathologic pro-inflammatory cytokines or related molecules leads to excellent therapeutic effects in inflammatory arthritis, including rheumatoid arthritis, ankylosing spondylitis, and psoriatic arthritis. Most of these agents, known as biologic disease-modifying anti-rheumatic drugs (bDMARDs), are produced in live cell lines and are usually monoclonal antibodies. Several types of monoclonal antibodies target different pro-inflammatory cytokines, such as tumor necrosis factor-α, interleukin (IL)-17A, IL-6, and IL-23/12. Some bDMARDs, such as rituximab and abatacept, target specific cell-surface molecules to control the inflammatory response. The therapeutic effects of these bDMARDs differ in different forms of inflammatory arthritis and are associated with different adverse events. In this article, we summarize the therapeutic utility and adverse effects of bDMARDs and suggest future research directions for developing bDMARDs.
Keyphrases
- rheumatoid arthritis
- ankylosing spondylitis
- disease activity
- inflammatory response
- cell surface
- oxidative stress
- interstitial lung disease
- rheumatoid arthritis patients
- anti inflammatory
- diffuse large b cell lymphoma
- lipopolysaccharide induced
- emergency department
- neoadjuvant chemotherapy
- immune response
- cancer therapy
- locally advanced
- systemic lupus erythematosus
- toll like receptor
- adverse drug
- idiopathic pulmonary fibrosis
- electronic health record