Covid19-Sources

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Effective strategies against COVID-19 and the importance of infection sequelae - Global Health Research and Policy
Effective strategies against COVID-19 and the importance of infection sequelae - Global Health Research and Policy
COVID-19 is a serious threat to human health and development. The acute burden of the pandemic includes more than 18.2 million deaths worldwide, and is unprecedented in modern times. This represents only a fraction of the total burden, as it excludes infection sequelae. An effective global strategic paradigm has been missing throughout the pandemic. The ‘flattening the curve’ approach neglected the importance of infection sequelae, and being centered on healthcare capacity was conceptually contrary to a people-centered health system. In March 2022, the World Health Organization revised its pandemic approach, importantly shifting emphasis away from managing transmission and towards prevention. Despite limitations, this now recognizes the role of infection sequelae, whose impact is becoming clearer in both variety and scale. Drawing on the foundational concepts of Sun Tzu and Carl von Clausewitz, most country approaches do not qualify as strategies, but rather as operational plans. They are also largely ineffective, neglecting infection sequelae, viral evolution dangers and other parameters. The purpose of this article is to summarize the evidence on COVID-19 infection sequelae, and alongside other contextual parameters use this to motivate that infection should be prevented. This is then used to answer the question: What is an effective strategy against COVID-19?
·ghrp.biomedcentral.com·
Effective strategies against COVID-19 and the importance of infection sequelae - Global Health Research and Policy
Cardiovascular Disease and COVID-19: Insight From Cases With Heart Failure
Cardiovascular Disease and COVID-19: Insight From Cases With Heart Failure
Recent evidence indicates that a large proportion of deaths from coronavirus disease 2019 (COVID-19) can be attributed to cardiovascular disease, including acute myocardial infarction, arrhythmias and heart failure. Indeed, severe infection increases the risk of heart failure among patients with COVID-19. In most patients, heart failure arises from complex interactions between pre-existing conditions, cardiac injury, renin-angiotensin system activation, and the effects of systemic inflammation on the cardiovascular system. In this review, we summarize current knowledge regarding pathogen-driven heart failure occurring during treatment for COVID-19, the potential effects of commonly used cardiovascular and anti-infective drugs in these patients, and possible directions for establishing a theoretical basis for clinical treatment.
·frontiersin.org·
Cardiovascular Disease and COVID-19: Insight From Cases With Heart Failure
Beim Screening auch falsch-positive Tests in Betracht ziehen
Beim Screening auch falsch-positive Tests in Betracht ziehen
Ein sicheres Verfahren zum Nachweis einer frühen SARS-CoV-2-Infektion ist der RT-PCR (Reverse Transkriptase-Polymerase-Kettenreaktion)-Test. Das Beispiel einer symptomfreien Patientin mit fünf PCR-Tests in knapp drei Wochen, von denen ausschließlich der mittlere positiv ausfiel, zeigt jedoch, dass man auch mit falsch-positiven Ergebnissen rechnen muss.
·ncbi.nlm.nih.gov·
Beim Screening auch falsch-positive Tests in Betracht ziehen
Dr Elisa Perego on Twitter
Dr Elisa Perego on Twitter
"Thromboembolism (TE) rates of COVID-19 are high and associated with higher risk of death. Robust evidence from ongoing clinical trials is needed to determine the impact of thromboprophylaxis on TE and mortality risk of COVID-19."—2020. Still waiting?https://t.co/M7railWlMe— Dr Elisa Perego (@elisaperego78) December 1, 2022
·twitter.com·
Dr Elisa Perego on Twitter
Bert Weingarten on Twitter
Bert Weingarten on Twitter
#LongCovid bei KindernEine Zusammenfassung von Studien und Meldungen:Klinische Merkmale, Aktivitätsniveaus und psychische Gesundheitsprobleme bei #Kindern mit LongCovid— Bert Weingarten (@WeingartenDE) March 12, 2021
·twitter.com·
Bert Weingarten on Twitter
Cutting Edge: Circulating Exosomes with COVID Spike Protein Are Induced by BNT162b2 (Pfizer–BioNTech) Vaccination prior to Development of Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines
Cutting Edge: Circulating Exosomes with COVID Spike Protein Are Induced by BNT162b2 (Pfizer–BioNTech) Vaccination prior to Development of Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines
Key Points. BNT162b2 induces release of exosomes carrying SARS-CoV-2 spike protein.Abs to SARS-CoV-2 develop after detection of circulatory exosomes.Exosomes wi
·journals.aai.org·
Cutting Edge: Circulating Exosomes with COVID Spike Protein Are Induced by BNT162b2 (Pfizer–BioNTech) Vaccination prior to Development of Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines
The Impact of Long COVID on Health, Society, and Economies
The Impact of Long COVID on Health, Society, and Economies
The Impact of Long COVID on Health, Society, and Economies A World Health Network Virtual Symposium Join us for our long COVID symposium! This global event brings together clinicians, researchers and patients to explore the latest advances in long COVID research and the impacts on health, society, and economies. With every passing day, we find more evidence that getting infected, or reinfected by COVID leads to the risk of chronic disease, long-term disability, and increased risk of heart attacks, strokes, brain damage, and impairment of the immune system. We see a worsening impact on families, communities, the workforce, and the economy. This symposium will cover key aspects of long COVID and the latest research findings, including: What is long COVID? What does it mean to live with it? How does it manifest? What are the underlying disease mechanisms? What can we do if we have long COVID? How can we protect ourselves?
·youtube.com·
The Impact of Long COVID on Health, Society, and Economies
Persistent post–COVID-19 smell loss is associated with immune cell infiltration and altered gene expression in olfactory epithelium
Persistent post–COVID-19 smell loss is associated with immune cell infiltration and altered gene expression in olfactory epithelium
SARS-CoV-2 causes profound changes in the sense of smell, including total smell loss. Although these alterations are often transient, many patients with COVID-19 exhibit olfactory dysfunction that lasts months to years. Although animal and human autopsy studies have suggested mechanisms driving acute anosmia, it remains unclear how SARS-CoV-2 causes persistent smell loss in a subset of patients. To address this question, we analyzed olfactory epithelial samples collected from 24 biopsies, including from nine patients with objectively quantified long-term smell loss after COVID-19. This biopsy-based approach revealed a diffuse infiltrate of T cells expressing interferon-γ and a shift in myeloid cell population composition, including enrichment of CD207+ dendritic cells and depletion of anti-inflammatory M2 macrophages. Despite the absence of detectable SARS-CoV-2 RNA or protein, gene expression in the barrier supporting cells of the olfactory epithelium, termed sustentacular cells, appeared to reflect a response to ongoing inflammatory signaling, which was accompanied by a reduction in the number of olfactory sensory neurons relative to olfactory epithelial sustentacular cells. These findings indicate that T cell–mediated inflammation persists in the olfactory epithelium long after SARS-CoV-2 has been eliminated from the tissue, suggesting a mechanism for long-term post–COVID-19 smell loss.
·science.org·
Persistent post–COVID-19 smell loss is associated with immune cell infiltration and altered gene expression in olfactory epithelium
Todesursachenstatistik 2021: 7 % aller Todesfälle gehen direkt auf COVID-19 zurück
Todesursachenstatistik 2021: 7 % aller Todesfälle gehen direkt auf COVID-19 zurück
Im Jahr 2021 sind in Deutschland nach endgültigen Ergebnissen der Todesursachenstatistik insgesamt 1 023 687 Menschen verstorben, davon waren 515 559 Männer und 508 128 Frauen. Wie das Statistische Bundesamt (Destatis) weiter mitteilt, stieg die Zahl der Todesfälle damit um 3,9 % gegenüber dem Vorjahr (2020: 985 572 Verstorbene). An COVID-19 als Grundleiden verstarben im Jahr 2021 in Deutschland insgesamt 71 331 Menschen, das waren 79 % mehr als im Vorjahr (2020: 39 758). Damit war COVID-19 bei 7,0 % aller Verstorbenen die ausschlaggebende Todesursache.
·destatis.de·
Todesursachenstatistik 2021: 7 % aller Todesfälle gehen direkt auf COVID-19 zurück
The durability of natural infection and vaccine-induced immunity against future infection by SARS-CoV-2
The durability of natural infection and vaccine-induced immunity against future infection by SARS-CoV-2
The durability of vaccine-mediated immunity to SARS-CoV-2, the durations to breakthrough infection, and the optimal timings of booster vaccination are crucial knowledge for pandemic response. Here, we applied comparative evolutionary analyses to estimate the durability of immunity and the likelihood of breakthrough infections over time following vaccination by BNT162b2 (Pfizer-BioNTech), mRNA-1273 (Moderna), ChAdOx1 (Oxford-AstraZeneca), and Ad26.COV2.S (Johnson & Johnson/Janssen). We evaluated anti-Spike (S) immunoglobulin G (IgG) antibody levels elicited by each vaccine relative to natural infection. We estimated typical trajectories of waning and corresponding infection probabilities, providing the distribution of times to breakthrough infection for each vaccine under endemic conditions. Peak antibody levels elicited by messenger RNA (mRNA) vaccines mRNA-1273 and BNT1262b2 exceeded that of natural infection and are expected to typically yield more durable protection against breakthrough infections (median 29.6 mo; 5 to 95% quantiles 10.9 mo to 7.9 y) than natural infection (median 21.5 mo; 5 to 95% quantiles 3.5 mo to 7.1 y). Relative to mRNA-1273 and BNT1262b2, viral vector vaccines ChAdOx1 and Ad26.COV2.S exhibit similar peak anti-S IgG antibody responses to that from natural infection and are projected to yield lower, shorter-term protection against breakthrough infection (median 22.4 mo and 5 to 95% quantiles 4.3 mo to 7.2 y; and median 20.5 mo and 5 to 95% quantiles 2.6 mo to 7.0 y; respectively). These results leverage the tools from evolutionary biology to provide a quantitative basis for otherwise unknown parameters that are fundamental to public health policy decision-making.
Peak antibody levels elicited by messenger RNA (mRNA) vaccines mRNA-1273 and BNT1262b2 exceeded that of natural infection and are expected to typically yield more durable protection against breakthrough infections (median 29.6 mo; 5 to 95% quantiles 10.9 mo to 7.9 y) than natural infection (median 21.5 mo; 5 to 95% quantiles 3.5 mo to 7.1 y). Relative to mRNA-1273 and BNT1262b2, viral vector vaccines ChAdOx1 and Ad26.COV2.S exhibit similar peak anti-S IgG antibody responses to that from natural infection and are projected to yield lower, shorter-term protection against breakthrough infection (median 22.4 mo and 5 to 95% quantiles 4.3 mo to 7.2 y; and median 20.5 mo and 5 to 95% quantiles 2.6 mo to 7.0 y; respectively).
·pnas.org·
The durability of natural infection and vaccine-induced immunity against future infection by SARS-CoV-2
SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination
SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination
The decline in nasal IgA responses 9 months after infection and minimal impact of subsequent vaccination may explain the lack of long-lasting nasal defence against reinfection and the limited effects of vaccination on transmission. These findings highlight the need to develop vaccines that enhance nasal immunity.
·thelancet.com·
SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination
Pediatric health system impact of an early respiratory viral season in Eastern Ontario, Canada: A descriptive analysis
Pediatric health system impact of an early respiratory viral season in Eastern Ontario, Canada: A descriptive analysis
Background The current respiratory viral season in Ontario started early with an intensity experienced throughout the pediatric health system. We sought to examine trends in patient volumes and level of care intensity among children admitted with laboratory-confirmed respiratory viral infection over the last five years in Ottawa. Methods This was a retrospective cohort study of patients at CHEO, a pediatric health centre in Ottawa, who were diagnosed with a laboratory-confirmed respiratory viral infection in the first 72 hours of admission between October 22, 2017 and December 10, 2022. Their admissions were stratified by age groups and levels of care intensity and evaluated for trends over six surveillance periods that begin in Week 35 and end in Week 34 of the following calendar year. Results During this current surveillance period, there was an early, rapid, two-fold increase in admissions due to respiratory viral infections compared to previous periods, driven largely by RSV and influenza. While there were similar age distributions, there was a larger volume of Level 2 and 3 admissions, and higher proportion of patients requiring Level 2 intensity of care (20.8% versus 2.2% to 12.0% in pre-pandemic years; p
·medrxiv.org·
Pediatric health system impact of an early respiratory viral season in Eastern Ontario, Canada: A descriptive analysis
COVID-19 inhibits spermatogenesis in the testes by inducing cellular senescence
COVID-19 inhibits spermatogenesis in the testes by inducing cellular senescence
COVID-19 (SARS-CoV-2) has been linked to organ damage in humans since its worldwide outbreak. It can also induce severe sperm damage, according to research conducted at numerous clinical institutions, however the exact mechanism of damage is still unknown. In this study, we downloaded testicular bulk-RNA-seq data from three COVID-19 patients and three uninfected controls from GEO to evaluate the effect of COVID-19 infection on spermatogenesis. By detecting the relative expression of each pathway and the correlation between genes or pathways, we found that COVID-19 could induce testicular cell senescence through MAPK signaling pathway. Cellular senescence was synergistic with MAPK pathway, which further affected the normal synthesis of cholesterol and androgen, inhibited the normal synthesis of lactate and pyruvate, and ultimately affected spermatogenesis. The medications targeting MAPK signaling pathway, especially MAPK1 and MAPK14, are expected to be effective therapeutic medications for reducing COVID-19 damage to spermatogenesis. These result give us a new understanding of how COVID-19 inhibits spermatogenesis and provide a possible solution to alleviate this damage.
·frontiersin.org·
COVID-19 inhibits spermatogenesis in the testes by inducing cellular senescence
Vaccine-induced systemic and mucosal T cell immunity to SARS-CoV-2 viral variants
Vaccine-induced systemic and mucosal T cell immunity to SARS-CoV-2 viral variants
The first-generation COVID-19 vaccines have been effective in mitigating severe illness and hospitalization, but recurring waves of infections are associated with the emergence of SARS-CoV-2 variants that display progressive abilities to evade antibodies, leading to diminished vaccine effectiveness. The lack of clarity on the extent to which vaccine-elicited mucosal or systemic memory T cells protect against such antibody-evasive SARS-CoV-2 variants remains a critical knowledge gap in our quest for broadly protective vaccines. Using adjuvanted spike protein–based vaccines that elicit potent T cell responses, we assessed whether systemic or lung-resident CD4 and CD8 T cells protected against SARS-CoV-2 variants in the presence or absence of virus-neutralizing antibodies. We found that 1) mucosal or parenteral immunization led to effective viral control and protected against lung pathology with or without neutralizing antibodies, 2) protection afforded by mucosal memory CD8 T cells was largely redundant in the presence of antibodies that effectively neutralized the challenge virus, and 3) “unhelped” mucosal memory CD8 T cells provided no protection against the homologous SARS-CoV-2 without CD4 T cells and neutralizing antibodies. Significantly, however, in the absence of detectable virus-neutralizing antibodies, systemic or lung-resident memory CD4 and “helped” CD8 T cells provided effective protection against the relatively antibody-resistant B1.351 (β) variant, without lung immunopathology. Thus, induction of systemic and mucosal memory T cells directed against conserved epitopes might be an effective strategy to protect against SARS-CoV-2 variants that evade neutralizing antibodies. Mechanistic insights from this work have significant implications in the development of T cell–targeted immunomodulation or broadly protective SARS-CoV-2 vaccines.
·pnas.org·
Vaccine-induced systemic and mucosal T cell immunity to SARS-CoV-2 viral variants