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10.3390/vaccines8040673

http://scihub22266oqcxt.onion/10.3390/vaccines8040673
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33198287!7712722!33198287
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suck abstract from ncbi


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pmid33198287      Vaccines+(Basel) 2020 ; 8 (4): ä
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  • SARS-CoV-2 Proteins Induce IFNG in Th1 Lymphocytes Generated from CD4+ Cells from Healthy, Unexposed Polish Donors #MMPMID33198287
  • Salkowska A; Karwaciak I; Karas K; Dastych J; Ratajewski M
  • Vaccines (Basel) 2020[Nov]; 8 (4): ä PMID33198287show ga
  • The outbreak of the SARS-CoV-2 virus in December 2019 has caused the deaths of several hundred thousand people worldwide. Currently, the pathogenesis of COVID-19 is poorly understood. During the course of COVID-19 infection, many patients experience deterioration, which might be associated with systemic inflammation and cytokine storm syndrome; however, other patients have mild symptoms or are asymptomatic. There are some suggestions that impaired cellular immunity through a reduction in Th1 response and IFNG (interferon gamma) expression, as well as cross-reactivity with common cold coronaviruses, might be involved in the differential COVID-19 course. Here, we show that CD4+ cells isolated from unexposed healthy donors that were differentiated towards the Th1 lineage in the presence of SARS-CoV-2 proteins exhibited induction of IFNG. Interestingly, the same cells induced to differentiate towards a Th17 lineage did not exhibit changes in IFNG expression or Th17-related cytokines. This suggests the cellular response to SARS-CoV-2 viral proteins is primarily associated with Th1 lymphocytes and may be dependent on past infections with common cold coronaviruses or vaccinations that induce unspecific cellular responses, e.g., BCG (Bacillus Calmette-Guerin). Thus, our results might explain the high variability in the course of COVID-19 among populations of different countries.
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