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      Analyzing the role of HLA class I molecules in COVID-19 disease in Africa and around the world

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            Abstract

            The coronavirus disease 2019 (COVID-19) has left a devasting effect on various regions globally. Africa has exceptionally high rates of other infectious diseases such as tuberculosis (TB), Human Immunodeficiency virus (HIV), and malaria, and was not impacted by COVID-19 to the extent of other continents (1). Globally, COVID-19 caused approximately 7 million deaths and 700 million infections thus far. COVID-19 disease severity and susceptibility vary among individuals and populations which could be attributed to various factors including the viral strain, host genetics, environment, lifespan, and co-existing conditions. Host genetics play a substantial part in COVID-19 disease severity among individuals. Human leukocyte antigen (HLA) was previously shown to be very important across host immune responses against viruses. HLA has been a widely studied gene region for various disease associations that have been identified. HLA proteins present peptides to the cytotoxic lymphocytes which causes an immune response to kill infected cells. The HLA molecule serves as the central region for infectious disease association; therefore, we expect HLA disease association with COVID-19. Therefore, in this review, we look at the HLA gene region, particularly, HLA class I, and understand its role in COVID-19 disease.

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            Author and article information

            Journal
            ScienceOpen Preprints
            ScienceOpen
            5 March 2024
            Affiliations
            [1 ] University of KwaZulu Natal ;
            [2 ] University of KwaZulu-Natal;
            [3 ] University of KwaZulu Natal;
            Author notes
            Author information
            https://orcid.org/0000-0001-6708-8260
            Article
            10.14293/PR2199.000742.v1
            812167c4-ecf8-4141-8ba5-74c247b34503

            This work has been published open access under Creative Commons Attribution License CC BY 4.0 , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Conditions, terms of use and publishing policy can be found at www.scienceopen.com .

            History
            : 5 March 2024
            Categories

            Data sharing not applicable to this article as no datasets were generated or analysed during the current study.
            Human biology,Genetics,Microbiology & Virology

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