In Vitro Combinatorial Activity of Direct Acting Antivirals and Monoclonal Antibodies against the Ancestral B.1 and BQ.1.1 SARS-CoV-2 Viral Variants DOI Open Access
Lia Fiaschi,

Camilla Biba,

Ilenia Varasi

et al.

Published: Jan. 3, 2024

Combination antiviral therapy may be helpful in the treatment of SARS-CoV-2 infection, however no clinical trial data are available and combined use direct acting antivirals (DAA) monoclonal antibodies (mAb) has been reported only anecdotally. To assess cooperative effects dual drug combinations vitro, we used a VERO E6 cell based vitro system with ancestral B.1 or highly divergent BQ.1.1 virus to test pairwise licensed DAA, including nirmatrelvir (NRM), remdesivir (RDV) active metabolite molnupiravir (EIDD-1931) as well combination RDV four mAbs (sotrovimab, bebtelovimab, cilgavimab, tixagevimab; tested susceptible virus). According SynergyFinder 3.0 summary weighted scores, all had an additive effect. Within DAA/DAA combinations, paired scores variants were comparable. In post-hoc analysis weighting synergy by concentrations, several cases synergistic detected at specific both for RDV/mAb combinations. This was supported confirmation experiments showing more than linear shift effective concentration (IC50) increasing concentrations companion drug, although effect prominent but minimal null These results support which should further investigated animal models before introduction into clinic.

Language: Английский

Longitudinal Assessment of Solid Organ Transplant Recipients With SARS-CoV-2 Infection DOI
William C. Vuyk, Max Bobholz, Isla Emmen

et al.

Transplantation Proceedings, Journal Year: 2025, Volume and Issue: unknown

Published: May 1, 2025

Language: Английский

Citations

0

Clinical and Analytical Performance of ELISA Salivary Serologic Assay to Detect SARS-CoV-2 IgG in Children and Adults DOI Creative Commons
Andrea Padoan,

Chiara Cosma,

Costanza Di Chiara

et al.

Antibodies, Journal Year: 2024, Volume and Issue: 13(1), P. 6 - 6

Published: Jan. 5, 2024

Saliva is a promising matrix with several purposes. Our aim to verify if salivary anti-SARS-CoV-2 antibody determination suitable for monitoring immune responses. One hundred eighty-seven subjects were enrolled at University-Hospital Padova: 105 females (56.1%) and 82 males (43.9%), 95 (50.8%) children 92 (49.2%) adults. Subjects self-collected saliva using Salivette; nineteen collected three different samples within the day. A serum sample was obtained all individuals. The N/S IgG (sal-IgG) S-RBD (ser-IgG) used determining antibodies. mean (min-max) age 9.0 (1-18) 42.5 (20-61) Of 187 samples, 63 negative sal-IgG (33.7%), while 7 ser-IgG (3.7%). Spearman's correlation 0.56 (

Language: Английский

Citations

3

Substantial reduction in the clinical and economic burden of disease following variant-adapted mRNA COVID-19 vaccines in immunocompromised patients in France DOI Open Access
Amy S. Lee, Benjamin Davido, Ekkehard Beck

et al.

medRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: March 15, 2024

ABSTRACT An economic evaluation was conducted to predict the and clinical burden of vaccinating immunocompromised (IC) individuals aged ≥30 years with mRNA-1273 variant-adapted COVID-19 vaccines in Fall 2023 Spring 2024 versus BNT162b2 France. The number symptomatic infections, hospitalizations, deaths, long COVID cases, costs quality-adjusted life (QALYs) estimated using a static decision-analytic model. Predicted vaccine effectiveness (VE) were based on real-world data from prior versions, suggesting higher protection against infection hospitalization vaccines. VE estimates combined incidence probability severe outcomes. Uncertainty surrounding VE, coverage, incidence, mortality rates, QALYs tested sensitivity analyses. is predicted prevent an additional 3,882 357 81 326 cases when compared 230,000 IC individuals. This translates €10.1 million cost-savings societal perspective 645 saved. Results consistent across all analyses most sensitive variations coverage. These findings highlight importance increasing ability induce levels formulations this vulnerable population.

Language: Английский

Citations

3

Synergistic antimicrobial nanofiber membranes based on metal incorporated silica nanoparticles as advanced antimicrobial layers DOI Creative Commons
Piumika Yapa, Imalka Munaweera, Manjula Weerasekera

et al.

RSC Advances, Journal Year: 2024, Volume and Issue: 14(46), P. 33919 - 33940

Published: Jan. 1, 2024

In this post-new-normal era, the public prioritizes preventive measures over curing, which is a constructive approach to staying healthy. study, an innovative antimicrobial membrane material has been developed, showcasing promising potential for various applications. The metal-doped silica nanoparticles (Ag, Cu, and Co) were incorporated into cellulose acetate (CA) polymer-based nanofiber using electrospinning technique. metal doped silanol network of nanoparticles. fabricated membranes underwent detailed characterization wide range techniques including PXRD, FTIR, Raman, SEM, TEM, TGA, tensile testing. These analyses provided compelling evidence confirming successful incorporation cellulose-based nanofibers. band gap energies CA mats lie below 3.00 eV, that they are visible light active. trimetallic nanohybrid exhibited lowest energy 2.84 proving self-sterilizing ability mats. DPPH assay further confirmed best radical scavenging activity by mat (91.77 ± 0.88%). was assessed bacterial ATCC strains

Language: Английский

Citations

3

In Vitro Combinatorial Activity of Direct Acting Antivirals and Monoclonal Antibodies against the Ancestral B.1 and BQ.1.1 SARS-CoV-2 Viral Variants DOI Open Access
Lia Fiaschi,

Camilla Biba,

Ilenia Varasi

et al.

Published: Jan. 3, 2024

Combination antiviral therapy may be helpful in the treatment of SARS-CoV-2 infection, however no clinical trial data are available and combined use direct acting antivirals (DAA) monoclonal antibodies (mAb) has been reported only anecdotally. To assess cooperative effects dual drug combinations vitro, we used a VERO E6 cell based vitro system with ancestral B.1 or highly divergent BQ.1.1 virus to test pairwise licensed DAA, including nirmatrelvir (NRM), remdesivir (RDV) active metabolite molnupiravir (EIDD-1931) as well combination RDV four mAbs (sotrovimab, bebtelovimab, cilgavimab, tixagevimab; tested susceptible virus). According SynergyFinder 3.0 summary weighted scores, all had an additive effect. Within DAA/DAA combinations, paired scores variants were comparable. In post-hoc analysis weighting synergy by concentrations, several cases synergistic detected at specific both for RDV/mAb combinations. This was supported confirmation experiments showing more than linear shift effective concentration (IC50) increasing concentrations companion drug, although effect prominent but minimal null These results support which should further investigated animal models before introduction into clinic.

Language: Английский

Citations

2