Present Status and Future Trends of Natural-Derived Compounds Targeting T Helper (Th) 17 and Microsomal Prostaglandin E Synthase-1 (mPGES-1) as Alternative Therapies for Autoimmune and Inflammatory-Based Diseases

Molecules. 2020 Dec 18;25(24):6016. doi: 10.3390/molecules25246016.

Abstract

Several natural-based compounds and products are reported to possess anti-inflammatory and immunomodulatory activity both in vitro and in vivo. The primary target for these activities is the inhibition of eicosanoid-generating enzymes, including phospholipase A2, cyclooxygenases (COXs), and lipoxygenases, leading to reduced prostanoids and leukotrienes. Other mechanisms include modulation of protein kinases and activation of transcriptases. However, only a limited number of studies and reviews highlight the potential modulation of the coupling enzymatic pathway COX-2/mPGES-1 and Th17/Treg circulating cells. Here, we provide a brief overview of natural products/compounds, currently included in the Italian list of botanicals and the BELFRIT, in different fields of interest such as inflammation and immunity. In this context, we focus our opinion on novel therapeutic targets such as COX-2/mPGES-1 coupling enzymes and Th17/Treg circulating repertoire. This paper is dedicated to the scientific career of Professor Nicola Mascolo for his profound dedication to the study of natural compounds.

Keywords: BELFRIT; Th17; immunity; mPGES-1; natural compounds.

Publication types

  • Review

MeSH terms

  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Autoimmune Diseases / drug therapy*
  • Autoimmune Diseases / metabolism
  • Biological Products / chemistry
  • Biological Products / pharmacology*
  • Complementary Therapies
  • Cyclooxygenase 1 / metabolism*
  • Cyclooxygenase 2 / metabolism
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Microsomes / drug effects
  • Microsomes / metabolism
  • Th17 Cells

Substances

  • Anti-Inflammatory Agents
  • Biological Products
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human