COVID-19: Mechanistic Model of the African Paradox Supports the Central Role of the NF-κB Pathway

Viruses. 2021 Sep 21;13(9):1887. doi: 10.3390/v13091887.

Abstract

The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has expanded into a global pandemic, with more than 220 million affected persons and almost 4.6 million deaths by 8 September 2021. In particular, Europe and the Americas have been heavily affected by high infection and death rates. In contrast, much lower infection rates and mortality have been reported generally in Africa, particularly in the sub-Saharan region (with the exception of the Southern Africa region). There are different hypotheses for this African paradox, including less testing, the young age of the population, genetic disposition, and behavioral and epidemiological factors. In the present review, we address different immunological factors and their correlation with genetic factors, pre-existing immune status, and differences in cytokine induction patterns. We also focus on epidemiological factors, such as specific medication coverage, helminth distribution, and malaria endemics in the sub-Saharan region. An analysis combining different factors is presented that highlights the central role of the NF-κB signaling pathway in the African paradox. Importantly, insights into the interplay of different factors with the underlying immune pathological mechanisms for COVID-19 can provide a better understanding of the disease and the development of new targets for more efficient treatment strategies.

Keywords: African paradox; COVID-19; Duffy antigen receptor for chemokines (DARC); NF-κB; SARS-CoV-2; chemokine; cytokine storm; helminth infection; macrophage polarization; malaria incidence.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Africa / epidemiology
  • Angiotensin-Converting Enzyme 2 / metabolism
  • Biomarkers
  • COVID-19 / epidemiology*
  • COVID-19 / immunology
  • COVID-19 / metabolism
  • COVID-19 / virology*
  • Comorbidity
  • Cytokines / metabolism
  • Disease Susceptibility
  • Geography, Medical
  • Global Health
  • Host-Pathogen Interactions*
  • Humans
  • Mortality
  • NF-kappa B / metabolism
  • Population Surveillance
  • SARS-CoV-2 / physiology*
  • Signal Transduction

Substances

  • Biomarkers
  • Cytokines
  • NF-kappa B
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2