TY - JOUR
T1 - Elevated Neopterin Levels Predict Fatal Outcome in SARS-CoV-2-Infected Patients
AU - Chauvin, Manon
AU - Larsen, Martin
AU - Quirant, Bibiana
AU - Quentric, Paul
AU - Dorgham, Karim
AU - Royer, Luca
AU - Vallet, Hélène
AU - Guihot, Amelie
AU - Combadiere, Behazine
AU - Combadière, Christophe
AU - Barallat, Jaume
AU - Mayaux, Julien
AU - Luyt, Charles-Edouard
AU - Mathian, Alexis
AU - Amoura, Zahir
AU - Boddaert, Jacques
AU - Arméstar, Fernando
AU - Gorochov, Guy
AU - Martínez Cáceres, Eva María
AU - Sauce, Delphine
PY - 2021
Y1 - 2021
N2 - Innate immune activation during Covid-19 infection is associated with pernicious clinical outcome. Coronavirus disease 2019 (Covid-19) is a worldwide threat that has already caused more than 3 000 000 deaths. It is characterized by different patterns of disease evolution depending on host factors among which old-age and pre-existing comorbidities play a detrimental role. Previous coronavirus epidemics, notably SARS-CoV, were associated with increased serum neopterin levels, which can be interpreted as a sign of acute innate immunity in response to viral infection. Here we hypothesize that neopterin may serve as a biomarker of SARS-CoV-2 viral infection and Covid-19 disease severity. We measured neopterin blood levels by ELISA. Seric concentration was quantified from 256 healthy donors and 374 Covid-19 patients at hospital admission. Enrolled Covid-19 patients were all symptomatic and displayed a large spectrum of comorbidities. Patients were followed until disease resolution or death. Severe and critically ill SARS-CoV-2 infected patients were characterized by a profound exacerbation of immune activation characterized by elevated neopterin blood levels. Systemic neopterin levels above 19nM stratified healthy individuals from Covid-19 patients with 87% specificity and 100% sensitivity. Moreover, systemic neopterin levels above 53nM differentiated non-survivors from survivors with 64% specificity and 100% sensitivity. We propose that neopterin concentration measured at arrival to hospital is a hallmark of severe Covid-19 and identifies a high-risk population of pernicious clinical outcome with a need for special medical care.
AB - Innate immune activation during Covid-19 infection is associated with pernicious clinical outcome. Coronavirus disease 2019 (Covid-19) is a worldwide threat that has already caused more than 3 000 000 deaths. It is characterized by different patterns of disease evolution depending on host factors among which old-age and pre-existing comorbidities play a detrimental role. Previous coronavirus epidemics, notably SARS-CoV, were associated with increased serum neopterin levels, which can be interpreted as a sign of acute innate immunity in response to viral infection. Here we hypothesize that neopterin may serve as a biomarker of SARS-CoV-2 viral infection and Covid-19 disease severity. We measured neopterin blood levels by ELISA. Seric concentration was quantified from 256 healthy donors and 374 Covid-19 patients at hospital admission. Enrolled Covid-19 patients were all symptomatic and displayed a large spectrum of comorbidities. Patients were followed until disease resolution or death. Severe and critically ill SARS-CoV-2 infected patients were characterized by a profound exacerbation of immune activation characterized by elevated neopterin blood levels. Systemic neopterin levels above 19nM stratified healthy individuals from Covid-19 patients with 87% specificity and 100% sensitivity. Moreover, systemic neopterin levels above 53nM differentiated non-survivors from survivors with 64% specificity and 100% sensitivity. We propose that neopterin concentration measured at arrival to hospital is a hallmark of severe Covid-19 and identifies a high-risk population of pernicious clinical outcome with a need for special medical care.
KW - SARS-CoV-2
KW - Biomarker
KW - Neopterin
KW - Clinical outcome
KW - Death
U2 - 10.3389/fcimb.2021.709893
DO - 10.3389/fcimb.2021.709893
M3 - Article
C2 - 34497777
SN - 2235-2988
VL - 11
JO - Frontiers in cellular and infection microbiology
JF - Frontiers in cellular and infection microbiology
ER -