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10.1016/j.intimp.2021.107825

http://scihub22266oqcxt.onion/10.1016/j.intimp.2021.107825
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34116286!8169316!34116286
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suck abstract from ncbi


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pmid34116286      Int+Immunopharmacol 2021 ; 98 (ä): 107825
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  • Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity #MMPMID34116286
  • Cuesta-Llavona E; Gomez J; Albaiceta GM; Amado-Rodriguez L; Garcia-Clemente M; Gutierrez-Rodriguez J; Lopez-Alonso I; Hermida T; Enriquez AI; Hernandez-Gonzalez C; Gil-Pena H; Dominguez-Garrido E; Perez-Oliveira S; Alvarez V; Lopez-Larrea C; Suarez-Alvarez B; Tranche S; Jimeno-Demuth FJ; Coto E
  • Int Immunopharmacol 2021[Sep]; 98 (ä): 107825 PMID34116286show ga
  • The chemokine receptor CCR5 has been implicated in COVID-19. CCR5 and its ligands are overexpressed in patients. The pharmacological targeting of CCR5 would improve the COVID-19 severity. We sought to investigate the role of the CCR5-Delta32 variant (rs333) in COVID-19. The CCR5-Delta32 was genotyped in 801 patients (353 in the intensive care unit, ICU) and 660 healthy controls, and the deletion was significantly less frequent in hospitalysed COVID-19 than in healthy controls (p = 0.01, OR = 0.66, 95%CI = 0.49-0.88). Of note, we did not find homozygotes among the patients, compared to 1% of the controls. The CCR5 transcript was measured in leukocytes from 85 patients and 40 controls. We found a significantly higher expression of the CCR5 transcript among the patients, with significant difference when comparing the non-deletion carriers (controls = 35; patients = 81; p = 0.01). ICU-patients showed non-significantly higher expression than no-ICU cases. Our study points to CCR5 as a genetic marker for COVID-19. The pharmacological targeting of CCR5 should be a promising treatment for COVID-19.
  • |*Genetic Variation[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |COVID-19/diagnosis/*genetics/virology[MESH]
  • |Case-Control Studies[MESH]
  • |Female[MESH]
  • |Genetic Predisposition to Disease[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Intensive Care Units[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Patient Admission[MESH]
  • |Phenotype[MESH]
  • |Receptors, CCR5/*genetics[MESH]
  • |Risk Assessment[MESH]
  • |Risk Factors[MESH]
  • |SARS-CoV-2/*pathogenicity[MESH]


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