Evaluation of the host immune response assay SeptiCyte RAPID for potential triage of COVID-19 patients

Author:

Montero Maria Milagro,Hardy-Werbin Max,Gonzalez-Gallardo Soledad,Torres Erica,Rueda Rebeca,Hannet Irene,Kirk James T.,Yager Thomas D.,Navalkar Krupa,Arenas Maria del Mar,Arietta-Aldea Itziar,Castañeda Silvia,Gómez-Junyent Joan,Gómez-Zorrilla Silvia,Guerri-Fernandez Roberto,Sanchez-Martinez Francisca,López-Montesinos Immaculada,Pelegrín Ivan,Sendra Elena,Sorlí Luisa,Villar-García Judith,Bellosillo BeatrizORCID,Horcajada Juan Pablo

Abstract

AbstractTools for the evaluation of COVID-19 severity would help clinicians with triage decisions, especially the decision whether to admit to ICU. The aim of this study was to evaluate SeptiCyte RAPID, a host immune response assay (Immunexpress, Seattle USA) as a triaging tool for COVID-19 patients requiring hospitalization and potentially ICU care. SeptiCyte RAPID employs a host gene expression signature consisting of the ratio of expression levels of two immune related mRNAs, PLA2G7 and PLAC8, measured from whole blood samples. Blood samples from 146 adult SARS-CoV-2 (+) patients were collected within 48 h of hospital admission in PAXgene blood RNA tubes at Hospital del Mar, Barcelona, Spain, between July 28th and December 1st, 2020. Data on demographics, vital signs, clinical chemistry parameters, radiology, interventions, and SeptiCyte RAPID were collected and analyzed with bioinformatics methods. The performance of SeptiCyte RAPID for COVID-19 severity assessment and ICU admission was evaluated, relative to the comparator of retrospective clinical assessment by the Hospital del Mar clinical care team. In conclusion, SeptiCyte RAPID was able to stratify COVID-19 cases according to clinical severity: critical vs. mild (AUC = 0.93, p < 0.0001), critical vs. moderate (AUC = 0.77, p = 0.002), severe vs. mild (AUC = 0.85, p = 0.0003), severe vs. moderate (AUC = 0.63, p = 0.05). This discrimination was significantly better (by AUC or p-value) than could be achieved by CRP, lactate, creatine, IL-6, or D-dimer. Some of the critical or severe cases had “early” blood draws (before ICU admission; n = 33). For these cases, when compared to moderate and mild cases not in ICU (n = 37), SeptiCyte RAPID had AUC = 0.78 (p = 0.00012). In conclusion, SeptiCyte RAPID was able to stratify COVID-19 cases according to clinical severity as defined by the WHO COVID-19 Clinical Management Living Guidance of January 25th, 2021. Measurements taken early (before a patient is considered for ICU admission) suggest that high SeptiScores could aid in predicting the need for later ICU admission.

Funder

U.S. Department of Health & Human Services | Biomedical Advanced Research and Development Authority

This work was also funded in part by Immunexpress, Inc.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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