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Research progress of epigallocatechin-3-gallate (EGCG) on anti-pathogenic microbes and immune regulation activities

Journal

FOOD & FUNCTION
Volume 12, Issue 20, Pages 9607-9619

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1fo01352a

Keywords

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Funding

  1. National Key R&D Program of China [2018YFC1604405]
  2. Guangxi Innovation Driven Development Special Fund Project [AA20302018-18, AA20302018-17]
  3. National Tea Industry Technology System Research Project of China [CARS-19-C01]
  4. National Natural Science Foundation Project of China [31471590, 31100501]
  5. Self-Science Foundation of Hunan Province, China [2019jj50237]

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The COVID-19 virus has spread globally by the end of 2019, posing a serious threat to public health. EGCG, as an anti-pathogenic microorganism drug, demonstrates both direct and indirect anti-infection effects by interfering with pathogenic microorganisms' adsorption, replication, biofilm formation, and toxin release, as well as regulating immune inflammation and antioxidation.
At the end of 2019, the COVID-19 virus spread worldwide, infecting millions of people. Infectious diseases induced by pathogenic microorganisms such as the influenza virus, hepatitis virus, and Mycobacterium tuberculosis are also a major threat to public health. The high mortality caused by infectious pathogenic microorganisms is due to their strong virulence, which leads to the excessive counterattack by the host immune system and severe inflammatory damage of the immune system. This paper reviews the efficacy, mechanism and related immune regulation of epigallocatechin-3-gallate (EGCG) as an anti-pathogenic microorganism drug. EGCG mainly shows both direct and indirect anti-infection effects. EGCG directly inhibits early infection by interfering with the adsorption on host cells, inhibiting virus replication and reducing bacterial biofilm formation and toxin release; EGCG indirectly inhibits infection by regulating immune inflammation and antioxidation. At the same time, we reviewed the bioavailability and safety of EGCG in vivo. At present, the bioavailability of EGCG can be improved to some extent using nanostructured drug delivery systems and molecular modification technology in combination with other drugs. This study provides a theoretical basis for the development of EGCG as an adjuvant drug for anti-pathogenic microorganisms.

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