Leflunomide: an immunomodulatory drug for the treatment of rheumatoid arthritis and other autoimmune diseases
Abstract
Leflunomide (Arava) has recently been approved by the Food and Drug Administration for the treatment of rheumatoid arthritis (RA). The drug, due to its protective effects on structural joint damage, has been classified as a disease modifying anti-rheumatic drug (DMARD). Leflunomide is structurally dissimilar from other drugs currently used to treat RA and exhibits a different mechanism of action. It has shown to be protective in a variety of animal models of arthritis and autoimmunity based on its immunomodulatory activity. Leflunomide is rapidly converted in vivo to its pharmacologically active metabolite A77 1726. This metabolite is a potent non-cytotoxic inhibitor of the enzyme dihydroorotate dehydrogenase (DHODH), a key enzyme in the de novo synthesis of uridine monophosphate (UMP). Activated lymphocytes depend on the pyrimidine de novo syntheses to fulfill their metabolic needs for clonal expansion and terminal differentiation into effector cells. De novo synthesis of pyrimidines is not only essential to provide precursors for new RNA and DNA synthesis, but also for phospholipid synthesis and the pyrimidine sugars necessary for protein glycosylation, which support the massive expansion in membrane biosynthesis to form daughter cells. This mechanism likely contributes to leflunomide's action as a DMARD in RA and other autoimmune diseases. This review is a summary of current in vivo and in vitro data, focussing primarily on the mechanism of action of leflunomide in RA.
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T cells require DHODH for clonal expansion and differentiation into effector cells.
“Consistent with their reliance on 1C metabolism, T cells require DHODH for clonal expansion and differentiation into effector cells.74”
From The multifaceted contributions of mitochondria to cellular metabolism (2018) · cites this paper as [74]
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The multifaceted contributions of mitochondria to cellular metabolism
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- Authors
- Herrmann, M. L., Schleyerbach, R., & Kirschbaum, B. J.
- Corresponding author
- Herrmann, Matthias L
- ORCID
- Herrmann, Matthias L
- Venue
- Immunopharmacology
- Publisher
- Elsevier BV
- Published
- 2000-05
- Volume
- 47
- Issue
- 2-3
- Pages
- 273-289
- ISSN
- 0162-3109 (ISSN-L)
- OpenAlex
- W1979811627
- Cited by
- 273
- References
- 142
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 12 · 2023: 16 · 2022: 15 · 2021: 8 · 2020: 8 · 2019: 9 · 2018: 9 · 2017: 11 · 2016: 8 · 2015: 14 · 2014: 9 · 2013: 11 · 2012: 11
- FWCI
- 2.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Immunopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
- Keywords
- leflunomide, rheumatoid arthritis, immunomodulation, disease-modifying antirheumatic drugs, dihydroorotate dehydrogenase inhibition, A771726, lymphocyte proliferation, autoimmune disease, structural joint damage
- MeSH terms
- Leflunomide, Dihydroorotate Dehydrogenase, Animals, Anti-Inflammatory Agents, Non-Steroidal, Arthritis, Rheumatoid, Autoimmune Diseases, Humans, Immunosuppressive Agents, Isoxazoles, Oxidoreductases, Pyrimidines, T-Lymphocytes, Oxidoreductases Acting on CH-CH Group Donors
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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