Transplantation and Cellular Therapy, Journal Year: 2024, Volume and Issue: 30(11), P. 1108.e1 - 1108.e11
Published: Aug. 23, 2024
Language: Английский
Transplantation and Cellular Therapy, Journal Year: 2024, Volume and Issue: 30(11), P. 1108.e1 - 1108.e11
Published: Aug. 23, 2024
Language: Английский
The Lancet Infectious Diseases, Journal Year: 2024, Volume and Issue: 24(7), P. e453 - e462
Published: Feb. 7, 2024
SARS-CoV-2 causes persistent infections in a subset of individuals, which is major clinical and public health problem that should be prioritised for further investigation several reasons. First, infection often goes unrecognised, therefore might affect substantial number people, particularly immunocompromised individuals. Second, the formation tissue reservoirs (including non-respiratory tissues) underlie pathophysiology require new strategies diagnosis treatment. Finally, replication, setting suboptimal immune responses, possible source new, divergent virus variants escape pre-existing immunity on individual population levels. Defining optimal diagnostic treatment patients with replication monitoring viral evolution are urgent medical priorities.
Language: Английский
Citations
66Heliyon, Journal Year: 2025, Volume and Issue: 11(2), P. e41980 - e41980
Published: Jan. 1, 2025
Language: Английский
Citations
3Infection, Journal Year: 2023, Volume and Issue: 52(3), P. 877 - 889
Published: Nov. 29, 2023
Prolonged shedding of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been observed in immunocompromised hosts. Early monotherapy with direct-acting antivirals or monoclonal antibodies, as recommended by the international guidelines, does not prevent this certainty. Dual therapies may therefore have a synergistic effect.
Language: Английский
Citations
24Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)
Published: Sept. 18, 2024
Language: Английский
Citations
14Clinical Microbiology and Infection, Journal Year: 2024, Volume and Issue: 30(8), P. 1012 - 1017
Published: April 18, 2024
Language: Английский
Citations
13Frontiers in Medicine, Journal Year: 2024, Volume and Issue: 11
Published: Feb. 29, 2024
Objectives The aim of the study was to describe a cohort B-cell-depleted immunocompromised (IC) patients with prolonged or relapsing COVID-19 treated monotherapy combination therapy. Methods This is multicenter observational retrospective conducted on IC consecutively hospitalized SARS-CoV-2 infection from November 2020 January 2023. subjects were stratified according anti-SARS-CoV-2 therapy received. Results Eighty-eight enrolled, 19 under and 69 population had history immunosuppression (median 2 B-cells/mm 3 , IQR 1–24 cells), residual hypogammaglobulinemia observed in 55 patients. A reduced length hospitalization time negative molecular nasopharyngeal swab (NPS) versus group observed. In univariable multivariable analyses, percentage change rate days NPS negativity showed significant reduction receiving compared those monotherapy. Conclusion persistent patients, it essential explore new therapeutic strategies such as multi-target (antiviral double antiviral plus antibody-based therapies) avoid viral shedding and/or severe infection.
Language: Английский
Citations
11International Journal of Antimicrobial Agents, Journal Year: 2024, Volume and Issue: 63(3), P. 107095 - 107095
Published: Jan. 21, 2024
Antivirals and monoclonal antibodies are available to lower progression risk in immunocompromised patients. However, combination therapy with both types of agents has not been studied. Single-centre prospective cohort study. We enrolled all patients who received treatment for mild-to-moderate COVID-19 from January 1st, 2022, October 30th, 2022. Primary endpoint was at 90 days, defined as hospital admission or death due and/or seronegative persistent Three hundred four (304) were included. 43 (14.1%) sotrovimab plus a direct-acting antiviral 261 (85.9%) monotherapy. outcome occurred more frequently after monotherapy (4.6% vs 0%, p=0.154). Among anti-Spike IgG titter below 750 BAU/mL, frequent (23.9% p=0.001), including COVID-related (15.2% p=0.014) (10.9% p=0.044). Combination associated (OR 0.08, 95% CI 0.01-0.64). Anti-S than BAU/mL previous antiCD20 higher 13.70, 2.77-67.68; OR 3.05, 1.20-10.94, respectively). In immunocompromised, an may be effective SARS-CoV2.
Language: Английский
Citations
9The Lancet Infectious Diseases, Journal Year: 2024, Volume and Issue: 24(11), P. 1213 - 1224
Published: July 15, 2024
Language: Английский
Citations
9International Journal of Infectious Diseases, Journal Year: 2023, Volume and Issue: 137, P. 55 - 59
Published: Sept. 30, 2023
After the third year of COVID-19 pandemic, most severe burden falls upon immunocompromised patients who cannot mount an endogenous immune response after both vaccination and/or natural infection. They also experience persistent SARS-CoV-2 infection with high viral loads often unsuccessfully managed by standard antiviral monotherapy regimen initially validated for treatment immunocompetent patients, only. The off-label prescription such regimens in is likely to drive emergence treatment-related escape, relapses, excess morbidity, and mortality from delayed underlying disorders. A possible approach mitigate consequence based on combined therapies.
Language: Английский
Citations
20Virology Journal, Journal Year: 2023, Volume and Issue: 20(1)
Published: Dec. 15, 2023
Abstract Background Morbidity and mortality are higher in immunocompromised patients affected by COVID-19 than the general population. Some authors have successfully used antiviral combination, but never early phase of infection. Methods We conducted a retrospective cohort study to determine efficacy safety combination two antivirals, with without monoclonal antibody (mAb), both (within 10 days symptoms) later (after days) SARS-CoV-2 infection admitted our Facility. Results treated 11 (seven an four late COVID-19) intravenous remdesivir plus five oral nirmatelvir/ritonavir, also combined sotrovimab 10/11 cases. Notably, all “early” reached virological clearance at day 30 from end therapy were alive well follow-up, whereas corresponding numbers “late” 50% 75%. Patients group more frequently needed oxygen supplementation (p = 0.015) steroid 0.045) during admission severity 0.017). Discussion The is tolerated associated 100% clearance. lower response rates disease severity, whether plays causative role such findings has yet be determined.
Language: Английский
Citations
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