Drug Candidates for Autoimmune Diseases.
Sabrina SaurinMyriam MeineckGerhard ErkelJason SirleafJulia Weinmann-MenkeAndrea PautzPublished in: Pharmaceuticals (Basel, Switzerland) (2022)
Most of the immunosuppressive drugs used in the clinic to prevent organ rejection or to treat autoimmune disorders were originally isolated from fungi or bacteria. Therefore, in addition to plants, these are valuable sources for identification of new potent drugs. Many side effects of established drugs limit their usage and make the identification of new immunosuppressants necessary. In this review, we present a comprehensive overview of natural products with potent anti-inflammatory activities that have been tested successfully in different models of chronic inflammatory autoimmune diseases. Some of these candidates already have passed first clinical trials. The anti-inflammatory potency of these natural products was often comparable to those of established drugs, and they could be used at least in addition to standard therapy to reduce their dose to minimize unwanted side effects. A frequent mode of action is the inhibition of classical inflammatory signaling pathways, such as NF-κB, in combination with downregulation of oxidative stress. A drawback for the therapeutic use of those natural products is their moderate bioavailability, which can be optimized by chemical modifications and, in addition, further safety studies are necessary. Altogether, very interesting candidate compounds exist which have the potential to serve as starting points for the development of new immunosuppressive drugs.
Keyphrases
- anti inflammatory
- oxidative stress
- signaling pathway
- clinical trial
- drug induced
- multiple sclerosis
- primary care
- dna damage
- emergency department
- randomized controlled trial
- cell proliferation
- ischemia reperfusion injury
- pi k akt
- stem cells
- epithelial mesenchymal transition
- immune response
- bone marrow
- climate change
- study protocol
- electronic health record
- endoplasmic reticulum stress
- smoking cessation
- cell therapy
- replacement therapy
- heat stress