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Updated: May 13, 2026

An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
Targeting kinases: a new approach to treating inflammatory rheumatic diseases
1School of Immunity and Inflammation, College of Medical & Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2WD, United Kingdom. d.simmons@bham.ac.uk
The development of orally active kinase inhibitors, such as Janus kinase (JAK) and spleen tyrosine kinase (Syk) inhibitors, offers new treatment options for autoimmune diseases like rheumatoid arthritis (RA). These targeted therapies are progressing through clinical trials, marking a significant advancement in patient care.
Area of Science:
- Pharmacology
- Immunology
- Drug Development
Background:
- Orally active kinase inhibitors have been a focus of research for twenty years.
- The FDA approved the first JAK inhibitor, tofacitinib, in 2012 for rheumatoid arthritis (RA).
- Intense research is ongoing to expand JAK inhibitor utility and develop selective profiles for autoimmune indications.
Purpose of the Study:
- To review the progress of orally active kinase inhibitors in autoimmune diseases.
- To highlight the advancements in JAK and Syk inhibitor development.
- To discuss the emergence of new therapeutic options for RA.
Main Methods:
- Review of research and development activities in kinase inhibitors.
- Analysis of clinical trial progress for JAK and Syk inhibitors.
- Examination of FDA approvals and ongoing drug development.
Main Results:
- The first oral JAK inhibitor (tofacitinib) was approved for RA in 2012.
- Syk inhibitors, like fostamatinib, are in Phase 3 trials.
- Several kinase inhibitors have advanced beyond Phase 2 trials, indicating therapeutic progress.
Conclusions:
- The last few years have been transformative for kinase inhibitors in autoimmune diseases.
- New oral treatment options are emerging for RA patients.
- Kinase inhibitors represent a significant advancement beyond traditional DMARDs and biologics.
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