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10.33549/physiolres.934647

http://scihub22266oqcxt.onion/10.33549/physiolres.934647
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33728925!8820511!33728925
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suck abstract from ncbi


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pmid33728925      Physiol+Res 2021 ; 70 (1): 111-115
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  • CCR5Delta32 deletion as a protective factor in Czech first-wave COVID-19 subjects #MMPMID33728925
  • Hubacek JA; Dusek L; Majek O; Adamek V; Cervinkova T; Dlouha D; Pavel J; Adamkova V
  • Physiol Res 2021[Mar]; 70 (1): 111-115 PMID33728925show ga
  • Infection by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease (COVID-19), has spread widely around the globe. Significant inter-individual differences have been observed during the course of the infection, which suggests that genetic susceptibility may be a contributing factor. CC chemokine receptor 5 (CCR5), which acts as a co-receptor for the entry of HIV-1 into cells, is promising candidate whose can have an influence on SARS-CoV-2 infection. A genetic mutation known as CCR5Delta32, consisting of a 32-nucleotide deletion, encodes a truncated protein that protects homozygous carriers of the deletion from HIV-1 infection. Similarly, inhibition of CCR5 seems to be protective against COVID-19. In our study, we successfully genotyped 416 first-wave SARS-CoV-2-positive infection survivors (164 asymptomatic and 252 symptomatic) for CCR5?32, comparing them with a population based sample of 2,404 subjects. We found the highest number (P=0.03) of CCR5Delta32 carriers in SARS-CoV-2-positive/COVID-19-asympto-matic subjects (23.8 %) and the lowest number in SARS-CoV-2-positive/COVID-19-symptomatic patients (16.7 %), with frequency in the control population in the middle (21.0 %). We conclude that the CCR5?32 I/D polymorphism may have the potential to predict the severity of SARS-CoV-2 infection.
  • |*Sequence Deletion[MESH]
  • |COVID-19/diagnosis/*genetics/virology[MESH]
  • |Case-Control Studies[MESH]
  • |Czech Republic[MESH]
  • |Gene Frequency[MESH]
  • |Genetic Association Studies[MESH]
  • |Genetic Predisposition to Disease[MESH]
  • |Humans[MESH]
  • |Phenotype[MESH]
  • |Protective Factors[MESH]
  • |Receptors, CCR5/*genetics[MESH]
  • |Risk Assessment[MESH]
  • |Risk Factors[MESH]


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