The protease encoded by the TMPRSS2 gene facilitates viral infections and has been implicated in the pathogenesis of SARS-CoV-2. We analyzed the TMPRSS2 sequence and correlated the protein variants with the clinical features of a cohort of 1177 patients affected by COVID-19 in Italy. Nine relatively common variants (allele frequency > 0.01) and six missense variants which may affect the protease activity according to PolyPhen-2 in HumVar-trained mode were identified. Among them, p.V197M (p.Val197Met) (rs12329760) emerges as a common variant that has a deleterious effect on the protease and a protective effect on the patients. Its role appears particularly relevant in two subgroups of patients-young males and elderly women-and among those affected by co-morbidities, where the variant frequency is higher among individuals who were mildly affected by the disease and did not need hospitalization or oxygen therapy than among those more severely affected, who required oxygen therapy, ventilation or intubation. This study provides useful information for the identification of patients at risk of developing a severe form of COVID-19, and encourages the usage of drugs affecting the expression of TMPRSS2 or inhibiting protein activity.

Monticelli, M., Mele, B.H., Benetti, E., Fallerini, C., Baldassarri, M., Furini, S., et al. (2021). Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women. GENES, 12(4), 1-15 [10.3390/genes12040596].

Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women

Benetti E.;Fallerini C.;Baldassarri M.;Furini S.;Frullanti E.;Mari F.;Renieri A.;Daga S.
Membro del Collaboration Group
;
Amitrano S.
Membro del Collaboration Group
;
Bruttini M.
Membro del Collaboration Group
;
Meloni I.
Membro del Collaboration Group
;
Montagnani F.
Membro del Collaboration Group
;
Palmieri M.;Fabbiani M.;Zanelli G.
Membro del Collaboration Group
;
Bargagli E.
Membro del Collaboration Group
;
Bergantini L.
Membro del Collaboration Group
;
D’alessandro M.
Membro del Collaboration Group
;
Cameli P.
Membro del Collaboration Group
;
Scolletta S.
Membro del Collaboration Group
;
Franchi F.
Membro del Collaboration Group
;
Mazzei M. A.
Membro del Collaboration Group
;
Guerrini S.
Membro del Collaboration Group
;
Conticini E.
Membro del Collaboration Group
;
Cantarini L.
Membro del Collaboration Group
;
Frediani B.
Membro del Collaboration Group
;
Valente S.;Mandalà M.
Membro del Collaboration Group
;
Salerni L.
Membro del Collaboration Group
;
2021-01-01

Abstract

The protease encoded by the TMPRSS2 gene facilitates viral infections and has been implicated in the pathogenesis of SARS-CoV-2. We analyzed the TMPRSS2 sequence and correlated the protein variants with the clinical features of a cohort of 1177 patients affected by COVID-19 in Italy. Nine relatively common variants (allele frequency > 0.01) and six missense variants which may affect the protease activity according to PolyPhen-2 in HumVar-trained mode were identified. Among them, p.V197M (p.Val197Met) (rs12329760) emerges as a common variant that has a deleterious effect on the protease and a protective effect on the patients. Its role appears particularly relevant in two subgroups of patients-young males and elderly women-and among those affected by co-morbidities, where the variant frequency is higher among individuals who were mildly affected by the disease and did not need hospitalization or oxygen therapy than among those more severely affected, who required oxygen therapy, ventilation or intubation. This study provides useful information for the identification of patients at risk of developing a severe form of COVID-19, and encourages the usage of drugs affecting the expression of TMPRSS2 or inhibiting protein activity.
2021
Monticelli, M., Mele, B.H., Benetti, E., Fallerini, C., Baldassarri, M., Furini, S., et al. (2021). Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women. GENES, 12(4), 1-15 [10.3390/genes12040596].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/1143584