Corona in general

Corona in general

689 bookmarks
Custom sorting
Hypertonic saline solution shown to inhibit replication of SARS-CoV-2
Hypertonic saline solution shown to inhibit replication of SARS-CoV-2
Researchers at the University of São Paulo (USP) in Brazil have shown that a hypertonic saline solution inhibits replication of SARS-CoV-2, the virus that causes COVID-19, and have elucidated the biochemical mechanism involved. // 22.9.2021
·news-medical.net·
Hypertonic saline solution shown to inhibit replication of SARS-CoV-2
Detecting early outcomes in COVID-19 patients
Detecting early outcomes in COVID-19 patients
A new Nature study aimed to predict clinical data of COVID-19 patients based on clinical outcomes. // 21.9.2021
·news-medical.net·
Detecting early outcomes in COVID-19 patients
Dynamics of innate immune responses decide COVID-19 severity in genetically diverse mice
Dynamics of innate immune responses decide COVID-19 severity in genetically diverse mice
In a recently published article on the bioRxiv* preprint server, scientists from the USA and UK have described the significance of early inflammatory signaling pathways in determining the severity of coronavirus disease 2019 (COVID-19). // 21.9.2021
·news-medical.net·
Dynamics of innate immune responses decide COVID-19 severity in genetically diverse mice
Changes in fibrin clot structure contributes to thrombosis risk in severe COVID-19
Changes in fibrin clot structure contributes to thrombosis risk in severe COVID-19
Researchers from Europe recently demonstrated altered levels of factor XII (FXII) and its activation products in 2 independent cohorts of critically ill patients with COVID-19 compared to patients suffering from severe acute respiratory distress syndrome caused by the influenza virus (acute respiratory distress syndrome (ARDS)-influenza). // 21.9.2021
·news-medical.net·
Changes in fibrin clot structure contributes to thrombosis risk in severe COVID-19
Scientists hypothesize SARS-CoV-2 cryptically circulating among humans before the current outbreak
Scientists hypothesize SARS-CoV-2 cryptically circulating among humans before the current outbreak
As nations begin to recover, researchers from the National Taiwan University and Academia Sinica in Taipei have been looking to identify the changes the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) underwent over the course of the pandemic in order to better understand why the disease showed such virulence. // 20.9.2021
·news-medical.net·
Scientists hypothesize SARS-CoV-2 cryptically circulating among humans before the current outbreak
EFFICACY OF THE MEASLES-MUMPS-RUBELLA (MMR) VACCINE IN THE REDUCING THE SEVERITY OF COVID-19: AN INTERIM ANALYSIS OF A RANDOMISED CONTROLLED CLINICAL TRIAL
EFFICACY OF THE MEASLES-MUMPS-RUBELLA (MMR) VACCINE IN THE REDUCING THE SEVERITY OF COVID-19: AN INTERIM ANALYSIS OF A RANDOMISED CONTROLLED CLINICAL TRIAL
Background: COVID–19 is still a challenge, both with regard to its treatment and to the actual efficacy of the vaccines available to date, especially with the emergence of new variants. We evaluated the efficacy of the measles–mumps–rubella (MMR) vaccine in preventing SARS–CoV–2 infection and severity of COVID–19 in health workers. Methods: This analysis includes data from one ongoing blinded, randomized, placebo–controlled trial with participants aged 18–60 years were randomly assigned to receive the MMR vaccine or a placebo. The primary efficacy analysis included all participants with a positive nasopharyngeal RT–PCR test since their inclusion. Results: The MMR vaccine did not prevent the SARS–CoV–2 infection. Participants in the MMR group, compared with those in the placebo group, had a 48% risk reduction in symptomatic COVID–19 (RR = 0.52; 95% CI: 0.33-0.83; p=0.004) and a 76% risk reduction in COVID–19 treatment (RR = 0.24; 95% CI: 0.06-0.88; p = 0.020) with one dose and a 51% risk reduction in COVID–19 symptoms (RR = 0.49; 95% CI: 0.31 – 0.78; p = 0.001) and a 78% risk reduction in COVID–19 treatment (RR = 0.22; 95% CI: 0.06-0.82; p = 0.015) with two doses. Conclusions: This interim analysis of an ongoing clinical trial suggests that compared with a placebo, the vaccine reduces the risk of COVID–19 symptoms and reduces the need for COVID–19 treatment. ### Competing Interest Statement The authors have declared no competing interest. ### Clinical Trial Brazilian Clinical Trials Registry (ReBEC RBR-2xd6dkj) https://ensaiosclinicos.gov.br/rg/RBR-2xd6dkj ### Funding Statement We would like to thank the Federal University of Santa Catarina (UFSC) and Santa Catarina State Research and Innovation Foundation (FAPESC) for financing the study; University Hospital Prof Polydoro Ernani de Sao Thiago (HU/UFSC/EBSERH) for the research site where the study was carried out; FiocruzBiomanguinhos Laboratory for the supply of vaccines; Santa Catarina State Health Secretariat (SES/SC) and Central Public Health Laboratory (LACEN) for conducting the RT PCR tests for SARS CoV 2; Florianopolis Municipal Health Department (SMS/PMF), Health Center of Sao Jose Citty Hall (SMS/PMSJ) and UFSC Health Sciences Center (CCS/UFSC) for the supply of consumables for the study. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The trial protocol was reviewed and approved by Ethics Committees of Federal University of Santa Catarina (number 4.254.143) and National Research Ethics Committee (number 4.274.984). All necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable. Yes The results of this study are preliminary and the study is ongoing. A complete de-identified patient dataset will be available upon completion of clinical trials and publication of the results of the completed study upon request to the corresponding author. // 20.9.2021
·medrxiv.org·
EFFICACY OF THE MEASLES-MUMPS-RUBELLA (MMR) VACCINE IN THE REDUCING THE SEVERITY OF COVID-19: AN INTERIM ANALYSIS OF A RANDOMISED CONTROLLED CLINICAL TRIAL
Study highlights the usefulness of organoids for basic research into coronaviruses
Study highlights the usefulness of organoids for basic research into coronaviruses
Researchers from the group of Hans Clevers in collaboration with the group of Bart Haagmans (Erasmus MC) established an organoid biobank to search for the genes that are essential for the spreading of a SARS-CoV2 infection. // 20.9.2021
·news-medical.net·
Study highlights the usefulness of organoids for basic research into coronaviruses
Did the coronavirus jump from animals to people...
Did the coronavirus jump from animals to people...
Nature - A preliminary analysis of viral genomes suggests the COVID-19 pandemic might have multiple animal origins – but the findings still have to be peer reviewed. // 16.8.2021
·nature.com·
Did the coronavirus jump from animals to people...