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Expression of SARS-CoV-2 Host Cell Entry Factors in Immune System Components of Healthy Individuals and Its Relevance for COVID-19 Immunopathology.
Kumar, Ashutosh; Kumar, Sujeet; Narayan, Ravi K; Kumari, Chiman; Pareek, Vikas; Prasoon, Pranav.
  • Kumar A; Etiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.
  • Kumar S; Department of Anatomy, All India Institute of Medical Sciences-Patna, (AIIMS-P), Patna, India.
  • Narayan RK; Etiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.
  • Kumari C; Centre for Proteomics and Drug Discovery, Amity Institute of Biotechnology, Amity University, Maharashtra, India.
  • Pareek V; Etiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.
  • Prasoon P; Department of Anatomy, All India Institute of Medical Sciences-Patna, (AIIMS-P), Patna, India.
Viral Immunol ; 34(5): 352-357, 2021 06.
Article in English | MEDLINE | ID: covidwho-1343610
ABSTRACT
Intense immunological dysregulation including immune cell lesions has been characteristically observed in severe cases of coronavirus disease-2019 (COVID-19), for which molecular mechanisms are not properly understood. A study of physiological expressions of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) host cell entry-related factors in immune system components may help explain molecular mechanisms involved in COVID-19 immunopathology. We analyzed transcriptomic and proteomic expression metadata for SARS-CoV-2 host cell entry receptor ACE2 and entry associated proteases (TMPRSS2, CTSL, and FURIN) in silico across immune system components including the blood lineage cells. ACE2 was not detected in any of the studied immune cell components; however, varying transcriptomic and proteomic expressions were observed for TMPRSS2, CTSL, and FURIN. Nondetectable expressions of SARS-CoV-2 host cell entry receptor ACE2 in immune system components or blood lineage cells indicate it does not mediate immune cell lesions in COVID-19. Alternative mechanisms need to be explored for COVID-19 immunopathogenesis.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Internalization / SARS-CoV-2 / COVID-19 Limits: Humans Language: English Journal: Viral Immunol Journal subject: Allergy and Immunology / Virology Year: 2021 Document Type: Article Affiliation country: Vim.2020.0277

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Internalization / SARS-CoV-2 / COVID-19 Limits: Humans Language: English Journal: Viral Immunol Journal subject: Allergy and Immunology / Virology Year: 2021 Document Type: Article Affiliation country: Vim.2020.0277