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Less Severe Cases of COVID-19 in Sub-Saharan Africa: Could Co-infection or a Recent History of Plasmodium falciparum Infection Be Protective?

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FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.565625

关键词

SARS-CoV-2; COVID-19; Plasmodium falciparum infection; co-infection; Sub-Saharan Africa

资金

  1. MRC [MC_UP_1204/10] Funding Source: UKRI

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The low cases of COVID-19 in Sub-Saharan Africa may be due to population characteristics, early lockdown measures, and potential underreporting, with recent malaria infection possibly offering protection against severe COVID-19 cases. The hypothesis suggests that immunological memory against malaria may prime cells for early phagocytosis of SARS-CoV-2, protecting individuals with recent malaria infection against COVID-19. This highlights the potential biological link between malaria and COVID-19 infection, emphasizing the importance of CD147 immunoglobulin as an entry point for both viruses.
Sub-Saharan Africa has generally experienced few cases and deaths of coronavirus disease 2019 (COVID-19). In addition to other potential explanations for the few cases and deaths of COVID-19 such as the population socio-demographics, early lockdown measures and the possibility of under reporting, we hypothesize in this mini review that individuals with a recent history of malaria infection may be protected against infection or severe form of COVID-19. Given that both the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Plasmodium falciparum (P. falciparum) merozoites bind to the cluster of differentiation 147 (CD147) immunoglobulin, we hypothesize that the immunological memory against P. falciparum merozoites primes SARS-CoV-2 infected cells for early phagocytosis, hence protecting individuals with a recent P. falciparum infection against COVID-19 infection or severity. This mini review therefore discusses the potential biological link between P. falciparum infection and COVID-19 infection or severity and further highlights the importance of CD147 immunoglobulin as an entry point for both SARS-CoV-2 and P. falciparum into host cells.

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