A potential therapeutic combination for treatment of COVID-19: Synergistic effect of DPP4 and RAAS suppression

Med Hypotheses. 2020 Nov:144:110186. doi: 10.1016/j.mehy.2020.110186. Epub 2020 Aug 14.

Abstract

COVID-19, caused by the novel coronavirus SARS-CoV-2, is an abbreviated name for coronavirus disease 2019. COVID-19 became a global pandemic in early 2020. It predominantly affects not only the upper and lower respiratory tract, but also multiple organs, including the kidney, heart, and brain. The mortality of COVID-19 patients is high in men and in elderly patients with age-related diseases such as hypertension and diabetes. The angiotensin converting enzyme-2 (ACE-2), a component in the renin-angiotensin-aldosterone system (RAAS), plays as cell surface receptors for SARS-CoV-2. A recent study proved that coronavirus SARS-CoV-2 also uses dipeptidyl peptidase-4 (DPP4, also known as adenosine deaminase complexing protein 2, CD26) as a co-receptor when entering cells. In addition, DPP4 is also implicated in the regulation of the immune response. Thus, the combination of DPP4 inhibition and suppression of ACE-2/RAAS may be a novel therapeutic strategy for combating this pandemic.

Keywords: Angiotensin converting enzyme-2; Coronavirus SARS-CoV-2; Dipeptidyl peptidase-4; Renin–angiotensin–aldosterone system.

MeSH terms

  • Aged
  • Angiotensin-Converting Enzyme 2 / metabolism
  • COVID-19 / complications
  • COVID-19 Drug Treatment*
  • Cytokines / metabolism
  • Diabetes Complications / drug therapy
  • Dipeptidyl Peptidase 4 / metabolism*
  • Humans
  • Hypertension / complications
  • Hypertension / drug therapy
  • Immune System
  • Inflammation
  • Male
  • Renin-Angiotensin System / drug effects*
  • SARS-CoV-2 / physiology
  • Virus Internalization
  • Virus Replication

Substances

  • Cytokines
  • DPP4 protein, human
  • Dipeptidyl Peptidase 4
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2