4.3 Article

Baricitinib for the treatment of rheumatoid arthritis and systemic lupus erythematosus: a 2019 update

Journal

EXPERT REVIEW OF CLINICAL IMMUNOLOGY
Volume 15, Issue 7, Pages 693-700

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/1744666X.2019.1608821

Keywords

Baricitinib; tofacitinib; JAK; STAT; rheumatoid arthritis

Categories

Funding

  1. Ministry of Health, Labor and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan (JSPS KAKENHI) [15K08790, 17K16218]
  3. University of Occupational and Environmental Health, Japan, through UOEH Grant for Advanced Research
  4. Grants-in-Aid for Scientific Research [17K16218] Funding Source: KAKEN

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Introduction: JAK, which constitutively binds to some cytokine receptors, plays an important role in cytokine signaling. While JAK is comprised of JAK1, JAK2, JAK3, and Tyk2, more than 40 types of cytokines transmit signals through JAK. Baricitinib is reported to be highly effective in the treatment of rheumatoid arthritis (RA) and is the second drug launched as a JAK inhibitor for RA. Area covered: We provide an overview of the mechanisms of action of baricitinib and its clinical implications in RA and other autoimmune diseases based on recent reports. This review outlines the mechanisms of action of baricitinib on human immune cells, the results of Phase III trials for RA, and the results of Phase II trials on SLE. Expert opinion: Baricitinib has potential to fine-tune various immune networks through a variety of mechanisms. Precision medicine is required in order to achieve maximum effects of targeted synthetic DMARDs including baricitinib and biological DMARDs in the future.

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