Type-I Interferon assessment in 45 minutes using the FilmArray® PCR platform in SARS-CoV-2 and other viral infections.
Marine Mommert-TriponMagali PerretMatthew HockinSébastien VielAlexandre BelotJean-Christophe RichardMehdi MezidiJean-Baptiste FassierEtienne Javouheynull nullnull nullnull nullAndrew HemmertFrançois MalletSophie Trouillet-AssantKaren Brengel-PescePublished in: European journal of immunology (2021)
Low concentrations of type-I interferon (IFN) in blood seem to be associated with more severe forms of Coronavirus disease 2019 (COVID-19). However, following the type-I interferon response (IR) in early stage disease is a major challenge. We evaluated detection of a molecular interferon signature on a FilmArray® system, which includes PCR assays for four interferon stimulated genes. We analyzed three types of patient populations: (i) children admitted to a pediatric emergency unit for fever and suspected infection, (ii) ICU-admitted patients with severe COVID-19, and (iii) healthcare workers with mild COVID-19. The results were compared to the reference tools, that is, molecular signature assessed with Nanostring® and IFN-α2 quantification by SIMOA® (Single MOlecule Array). A strong correlation was observed between the IR measured by the FilmArray®, Nanostring®, and SIMOA® platforms (r-Spearman 0.996 and 0.838, respectively). The FilmArray® panel could be used in the COVID-19 pandemic to evaluate the IR in 45-min with 2 min hand-on-time at hospitalization and to monitor the IR in future clinical trials.
Keyphrases
- sars cov
- coronavirus disease
- dendritic cells
- single molecule
- respiratory syndrome coronavirus
- early stage
- clinical trial
- immune response
- high throughput
- public health
- emergency department
- intensive care unit
- high resolution
- pulmonary embolism
- living cells
- genome wide
- radiation therapy
- mechanical ventilation
- dna methylation
- phase ii
- quantum dots
- bioinformatics analysis
- neoadjuvant chemotherapy