Synonyms
Indications
Thalidomide is a potent teratogen.
Because of observed potential to increase tumor necrosis factor alpha production in vivo and interleukin-2 and interferon gamma in vivo, thalidomide has limited utility in the dermatologic manifestations of HIV, Behcet’s disease, and graft-versus-host disease and is now being investigated for use in myelodysplastic disorders.
Mechanisms of Action
The teratogenic effect may be related to vascular disruption. As noted, it impacts immune function including increasing production of tumor necrosis factor alpha in vitro and interleukin-2 and interferon gamma in vivo.
Specific Compounds and Properties
The chemical name is N-pthaloylglutamide.
Clinical Use (Including Side Effects)
Thalidomide was initially developed in 1954 and licensed in 40 countries around the world for treatment of anxiety, insomnia, gastritis, and vomiting. It was marketed as safe for use in pregnancy. It was never approved by the Food and Drug...
References and Reading
Kontogiannis, V., & Powell, R. J. (2000). Use of thalidomide in dermatologic indications. BioDrugs, 13(4), 255–265.
Miller, M. T., & STromland, K. K. (2011). What can be learned from the thalidomide experience: An ophthalmologic perspective. Current Opinion in Ophthalmology, 22(5), 356–364.
Rodier, P. M. (2004). Environmental causes of central nervous system maldevelopment. Pediatrics, 113, 1076–1083.
Millrine, D., & Kishimoto, T. (2017). A brighter side to thalidomide: Its potential use in immunological disorders. Trends in Molecular Medicine, 23(4), 348–361. https://doi.org/10.1016/j.molmed2017.02.006.Epub. PMID 28285807.
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Hyman, S. (2018). Thalidomide. In: Volkmar, F. (eds) Encyclopedia of Autism Spectrum Disorders. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6435-8_41-3
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DOI: https://doi.org/10.1007/978-1-4614-6435-8_41-3
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