Wim Van Damme1, Richard Wamai2, Yibeltal Assefa3, Laurens Liesenborghs4, Dieudonné Mumba5. 1. Department of Public Health, Institute of Tropical Medicine, 2000 Antwerp, Belgium. Electronic address: wvdamme@itg.be. 2. Department of Cultures, Societies, and Global Studies, Northeastern University, Boston, MA, USA. 3. School of Public Health, the University of Queensland, Brisbane, QLD, Australia. 4. Outbreak Research Team, Institute of Tropical Medicine, 2000 Antwerp, Belgium. 5. Department of Parasitology, Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
We read with interest the COVID-19 Forecasting Team's description of the variation in COVID-19 infection–fatality ratio, confirming that differences in COVID-19 mortality between geographies are largely explained by the age structures of their populations. However, we fear that the lower than anticipated burden of severe COVID-19 in most of sub-Saharan Africa gets lost in estimations from models based on data from the few African countries that have reliable excess mortality data but are not representative of sub-Saharan Africa. Moreover, country-level estimates of COVID-19 infection–fatality ratio hide the observation that COVID-19 mortality in sub-Saharan Africa is highly concentrated in sections of the population with a more western lifestyle—usually wealthier individuals in urban centres. Such disparity is obvious for most people living in sub-Saharan Africa, where COVID-19 is sometimes popularly called “VIP disease” or “rich person disease”.We suspect that, besides a higher prevalence of obesity, hypertension, and diabetes among wealthier people, immunological factors are at play. Several studies associate chronic parasitic infection (more prevalent among people living in poverty with a less westernised lifestyle) with less severe clinical presentation of COVID-19.3, 4 Such findings are consistent with the importance of a diverse microbiome and chronic immune stimulation in maintaining a well trained immune system that is less likely to cause hyperinflammation, which is critical in severe COVID-19.Although unexplored, the notion that the better-off might fare worse is not unique to COVID-19 in sub-Saharan Africa. It is also consistently documented that autoimmune diseases, more prevalent in high-income countries, share a common pathway with severe COVID-19, linking reduced microbiome diversity to hyperinflammation, popularised as the hygiene hypothesis. Similar links have been documented in HIV serosurveys in the 2000s in sub-Saharan Africa, in which the better-off had higher risk of HIV infection.It is vital to deepen our understanding of microbiome diversity and linked immunological factors in the severity of COVID-19, and account for this when modelling COVID-19 infection–fatality ratios.
Authors: B Brett Finlay; Katherine R Amato; Meghan Azad; Martin J Blaser; Thomas C G Bosch; Hiutung Chu; Maria Gloria Dominguez-Bello; Stanislav Dusko Ehrlich; Eran Elinav; Naama Geva-Zatorsky; Philippe Gros; Karen Guillemin; Frédéric Keck; Tal Korem; Margaret J McFall-Ngai; Melissa K Melby; Mark Nichter; Sven Pettersson; Hendrik Poinar; Tobias Rees; Carolina Tropini; Liping Zhao; Tamara Giles-Vernick Journal: Proc Natl Acad Sci U S A Date: 2021-02-09 Impact factor: 11.205
Authors: Jane Achan; Asadu Serwanga; Humphrey Wanzira; Tonny Kyagulanyi; Anthony Nuwa; Godfrey Magumba; Stephen Kusasira; Isaac Sewanyana; Kevin Tetteh; Chris Drakeley; Fredrick Nakwagala; Helen Aanyu; Jimmy Opigo; Prudence Hamade; Madeleine Marasciulo; Byarugaba Baterana; James K Tibenderana Journal: Lancet Microbe Date: 2021-10-25