Type III interferons (IFN-III), also known as IFN-Lambda, have a pivotal role during SARS-CoV-2 infection. IFN-Lambda response among individuals is heterogeneous and its association with COVID-19 symptoms severity needs to be further clarified. We analyzed the genotype frequencies of IFNL4 single nucleotide polymorphism (SNP) rs11322783 in patients with COVID-19 (n = 128), in comparison with a validated data set of European healthy controls (n = 14152). The IFNL4 SNP was also analyzed according to the haematological and clinical parameters of patients with COVID-19. The distributions of IFNL4 genotypes among SARS-CoV-2 positive patients [TT/TT 41.4% (n = 53), TT/∆G 47.7% (n = 61) and ∆G/∆G 10.9% (n = 14)] and healthy controls were comparable. Different levels of white blood cells (p = 0.036) and neutrophils (p = 0.042) were found in the IFNL4 different genotypes in patients with COVID-19; the ∆G/∆G genotype was more represented in the groups with low white blood cells and neutrophils. There were no differences in major inflammation parameters (C-reactive protein, D-dimer, Albumin, and Lactate-dehydrogenase (LDH)] and survival rate according to the IFNL4 genotypes. In conclusion, although patients with COVID-19 did not exhibit a different distribution of the IFNL4 SNP, the ∆G/∆G genotype was associated with a lower count of immune cell populations. These findings need to be confirmed in larger groups of patients with COVID-19 and the role of IFNL4 SNP needs to be also investigated in other respiratory viral infections.

Distribution of Interferon Lambda 4 Single Nucleotide Polymorphism rs11322783 Genotypes in Patients with COVID-19 / Sorrentino, L.; Silvestri, V.; Oliveto, G.; Scordio, M.; Frasca, F.; Fracella, M.; Bitossi, C.; D'Auria, A.; Santinelli, L.; Gabriele, L.; Pierangeli, A.; Mastroianni, C. M.; D'Ettorre, G.; Antonelli, G.; Caruz, A.; Ottini, L.; Scagnolari, C.. - In: MICROORGANISMS. - ISSN 2076-2607. - 10:2(2022), pp. 1-11. [10.3390/microorganisms10020363]

Distribution of Interferon Lambda 4 Single Nucleotide Polymorphism rs11322783 Genotypes in Patients with COVID-19

Sorrentino L.;Silvestri V.;Oliveto G.;Scordio M.;Frasca F.;Fracella M.;Bitossi C.;D'auria A.;Santinelli L.;Pierangeli A.;Mastroianni C. M.;D'ettorre G.;Antonelli G.;Ottini L.;Scagnolari C.
Ultimo
2022

Abstract

Type III interferons (IFN-III), also known as IFN-Lambda, have a pivotal role during SARS-CoV-2 infection. IFN-Lambda response among individuals is heterogeneous and its association with COVID-19 symptoms severity needs to be further clarified. We analyzed the genotype frequencies of IFNL4 single nucleotide polymorphism (SNP) rs11322783 in patients with COVID-19 (n = 128), in comparison with a validated data set of European healthy controls (n = 14152). The IFNL4 SNP was also analyzed according to the haematological and clinical parameters of patients with COVID-19. The distributions of IFNL4 genotypes among SARS-CoV-2 positive patients [TT/TT 41.4% (n = 53), TT/∆G 47.7% (n = 61) and ∆G/∆G 10.9% (n = 14)] and healthy controls were comparable. Different levels of white blood cells (p = 0.036) and neutrophils (p = 0.042) were found in the IFNL4 different genotypes in patients with COVID-19; the ∆G/∆G genotype was more represented in the groups with low white blood cells and neutrophils. There were no differences in major inflammation parameters (C-reactive protein, D-dimer, Albumin, and Lactate-dehydrogenase (LDH)] and survival rate according to the IFNL4 genotypes. In conclusion, although patients with COVID-19 did not exhibit a different distribution of the IFNL4 SNP, the ∆G/∆G genotype was associated with a lower count of immune cell populations. These findings need to be confirmed in larger groups of patients with COVID-19 and the role of IFNL4 SNP needs to be also investigated in other respiratory viral infections.
2022
covid-19; ifn-lambda4; rs11322783; single nucleotide polymorphism
01 Pubblicazione su rivista::01a Articolo in rivista
Distribution of Interferon Lambda 4 Single Nucleotide Polymorphism rs11322783 Genotypes in Patients with COVID-19 / Sorrentino, L.; Silvestri, V.; Oliveto, G.; Scordio, M.; Frasca, F.; Fracella, M.; Bitossi, C.; D'Auria, A.; Santinelli, L.; Gabriele, L.; Pierangeli, A.; Mastroianni, C. M.; D'Ettorre, G.; Antonelli, G.; Caruz, A.; Ottini, L.; Scagnolari, C.. - In: MICROORGANISMS. - ISSN 2076-2607. - 10:2(2022), pp. 1-11. [10.3390/microorganisms10020363]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1613623
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