Impaired systemic nucleocapsid antigen clearance in severe COVID‐19 DOI Creative Commons
Christian Bauer, Elisabeth Mack,

Véronique Hefter

et al.

Journal of Medical Virology, Journal Year: 2023, Volume and Issue: 95(8)

Published: Aug. 1, 2023

The circulating nucleocapsid (NCP) antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is detectable in disease-2019 (COVID-19) patients. To better understand the biology disease severity, we investigated NCP clearance kinetics hospitalized COVID-19 Serum was quantified using a commercial NCP-specific enzyme-linked immunoassay patients (n = 63) during their hospital stay. Results were correlated to inflammation parameters, antibody response, and results SARS-CoV-2 PCR from nasopharyngeal swabs. We demonstrate that levels serum remained elevated 21/45 (46.7%) samples intensive care units (ICU) after >8 days postdiagnosis. proportion ICU with antigenemia declined only gradually 84.6% 25.0% over several weeks. This contrast complete all non-ICU 8 days, also mucosal virus as measured by PCR. Antigen associated higher IgG against S1 but not NCP. Clearance delayed >40% severely ill Thus, detected post diagnosis characteristic requiring care. Prospective trials should further investigate mechanistic biomarker.

Language: Английский

Cell surface RNA virus nucleocapsid proteins: a viral strategy for immunosuppression? DOI Creative Commons
Alberto Domingo López-Muñoz, Jonathan W. Yewdell

npj Viruses, Journal Year: 2024, Volume and Issue: 2(1)

Published: Sept. 2, 2024

Abstract Nucleocapsid protein (N), or nucleoprotein (NP) coats the genome of most RNA viruses, protecting and shielding from cytosolic RNAases innate immune sensors, plays a key role in virion biogenesis viral transcription. Often one highly expressed gene products, N induces strong antibody (Ab) T cell responses. different viruses is present on infected surface copy numbers ranging tens thousands to millions per cell, it can be released bind uninfected cells. Surface targeted by Abs, which contribute clearance via Fc-mediated cellular cytotoxicity. modulate host immunity sequestering chemokines (CHKs), extending prior findings that interferes with adaptive immunity. In this review, we consider aspects biology immunology describe its potential as target for anti-viral intervention.

Language: Английский

Citations

1

SARS-CoV-2 viral load is linked to remdesivir efficacy in severe Covid-19 admitted to intensive care DOI Creative Commons
Martin Balík,

P. Waldauf,

Ivana Jurisinova

et al.

Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)

Published: Sept. 6, 2024

Language: Английский

Citations

1

Positivization time of a COVID-19 rapid antigen self-test predicts SARS-CoV-2 viral load: a proof of concept DOI Open Access
Gian Luca Salvagno, Brandon Michael Henry, Giulio Bongiovanni

et al.

Clinical Chemistry and Laboratory Medicine (CCLM), Journal Year: 2022, Volume and Issue: 61(2), P. 316 - 322

Published: Oct. 31, 2022

This proof of concept study was aimed to validate the hypothesis that time positivization SARS-CoV-2 self-performed rapid diagnostic tests (RDTs) may reflect actual viral load in specimen.A positive sample with high diluted and concomitantly assayed molecular assay (Xpert Xpress SARS-CoV-2) RDT (COVID-VIRO ALL IN RDT). The (mean cycle threshold; Ct) values times these dilutions were plotted interpolated by calculating best fit. parameters this equation then used for converting into RDT-estimated Ct routine patient samples.The fit between measured could be achieved a 2-degree polynomial curve. exhibited correlation (r=0.996) excellent Deming (y=1.01 × x - 0.18) values. In 30 consecutive patients test, value r=0.522 (p=0.003). slightly improved 0.577 (Deming fit: y=0.44 + 11.08), displaying negligible bias (1.0; 95% CI, -0.2 2.2; p=0.105). Concordance at <20 cut-off 80%, 0.84 sensitivity 0.73 specificity.This demonstrates potential feasibility using RDTs garnering information on acute infection.

Language: Английский

Citations

7

Performance of Blood-Based Nucleocapsid Antigen Tests for Diagnosis of Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Infectious Viral Shedding: A Systematic Review DOI Creative Commons

Sujata Mathur,

Matthew So, Peggy Tahir

et al.

Open Forum Infectious Diseases, Journal Year: 2023, Volume and Issue: 10(8)

Published: July 10, 2023

Abstract Data on the performance of blood-based nucleocapsid antigen tests for diagnosing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and infectious viral shedding are limited. To address this knowledge gap, we conducted a systematic review to assess (N) in SARS-CoV-2 identifying infectiousness. This was registered PROSPERO (registration no. CRD42022339635). We comprehensively searched PubMed, Embase, Web Science, Coronavirus Research Database relevant studies published through 27 February 2023. Each study's risk bias evaluated using Quality Assessment Diagnostic Accuracy Studies (QUADAS-2) tool. Our findings indicate that N-antigen test is influenced by factors such as assay type, sampling timing, illness severity. Sensitive assays provide suitable methods viable screening laboratory diagnostic different clinical research settings during early phase illness.

Language: Английский

Citations

3

Impaired systemic nucleocapsid antigen clearance in severe COVID‐19 DOI Creative Commons
Christian Bauer, Elisabeth Mack,

Véronique Hefter

et al.

Journal of Medical Virology, Journal Year: 2023, Volume and Issue: 95(8)

Published: Aug. 1, 2023

The circulating nucleocapsid (NCP) antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is detectable in disease-2019 (COVID-19) patients. To better understand the biology disease severity, we investigated NCP clearance kinetics hospitalized COVID-19 Serum was quantified using a commercial NCP-specific enzyme-linked immunoassay patients (n = 63) during their hospital stay. Results were correlated to inflammation parameters, antibody response, and results SARS-CoV-2 PCR from nasopharyngeal swabs. We demonstrate that levels serum remained elevated 21/45 (46.7%) samples intensive care units (ICU) after >8 days postdiagnosis. proportion ICU with antigenemia declined only gradually 84.6% 25.0% over several weeks. This contrast complete all non-ICU 8 days, also mucosal virus as measured by PCR. Antigen associated higher IgG against S1 but not NCP. Clearance delayed >40% severely ill Thus, detected post diagnosis characteristic requiring care. Prospective trials should further investigate mechanistic biomarker.

Language: Английский

Citations

3