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1.
Medicine (Baltimore) ; 101(48): e31827, 2022 Dec 02.
Artículo en Inglés | MEDLINE | ID: covidwho-2161253

RESUMEN

BACKGROUND: Coronavirus disease 2019 (COVID-19) is an acute respiratory infectious disease that makes breathing difficult and is often accompanied by olfactory disorders and distension. Chinese herbal tonics, a special external treatment of traditional Chinese medicine, has shown beneficial effects in the treatment of olfactory disorders. Currently, there is a lack of systematic reviews on Chinese herbal tonics for the treatment of olfactory disorders. We conduct this study to evaluate the efficacy and safety of Chinese herbal tonics in the treatment of olfactory disorders. This study is designed to evaluate the effectiveness and safety of Chinese herbal tonics for olfactory disorders in COVID-19. METHODS: Randomized controlled trials from December 2019 to September 2022. will be included, without restrictions on language or publication date. PubMed, EMBASE, Cochrane Library, Web of Science, Chinese Biomedical Databases, China National Knowledge Infrastructure, Wanfang Database, and VIP Database were searched. Two researchers will independently select studies, extract data, and evaluate study quality. The Cochrane risk of bias tool for randomized trials will be used to assess the risk of bias in the included studies. Statistical analyses will be conducted using the Review Manager (RevMan 5.3, Cochrane Collaboration, Nordic Cochrane Center, Copenhagen, Denmark). RESULTS: This study aimed to prove the efficacy and safety of Chinese herbal tonics for olfactory disorders in patients with COVID-19. Our study provides a more accurate treatment method for olfactory disorders during COVID-19.We will publish our results in a peer-reviewed journal.


Asunto(s)
COVID-19 , Medicamentos Herbarios Chinos , Humanos , Lenguaje , Metaanálisis como Asunto , Revisiones Sistemáticas como Asunto
2.
iScience ; 25(4): 104043, 2022 Apr 15.
Artículo en Inglés | MEDLINE | ID: covidwho-1734555

RESUMEN

With the rapid emergence and spread of SARS-CoV-2 variants, development of vaccines with broad and potent protectivity has become a global priority. Here, we designed a lipid nanoparticle-encapsulated, nucleoside-unmodified mRNA (mRNA-LNP) vaccine encoding the trimerized receptor-binding domain (RBD trimer) and showed its robust capability in inducing broad and protective immune responses against wild-type and major variants of concern (VOCs) in the mouse model of SARS-CoV-2 infection. The protectivity was correlated with RBD-specific B cell responses especially the long-lived plasma B cells in bone marrow, strong ability in triggering BCR clustering, and downstream signaling. Monoclonal antibodies isolated from vaccinated animals demonstrated broad and potent neutralizing activity against VOCs tested. Structure analysis of one representative antibody identified a novel epitope with a high degree of conservation among different variants. Collectively, these results demonstrate that the RBD trimer mRNA vaccine serves as a promising vaccine candidate against SARS-CoV-2 variants and beyond.

3.
Sci Rep ; 11(1): 16945, 2021 08 20.
Artículo en Inglés | MEDLINE | ID: covidwho-1366831

RESUMEN

The patterns of respiratory virus illness are expressed differently between temperate and tropical climates. Tropical outbreaks often peak in wet seasons. Temperate outbreaks typically peak during the winter. The prevailing causal hypotheses focus on sunlight, temperature and humidity variations. Yet no consistent factors have been identified to sufficiently explain seasonal virus emergence and decline at any latitude. Here we demonstrate close connections among global-scale atmospheric circulations, IgE antibody enhancement through seasonal pollen inhalation, and respiratory virus patterns at any populated latitude, with a focus on the US. Pollens emerge each Spring, and the renewed IgE titers in the population are argued to terminate each winter peak of respiratory illness. Globally circulated airborne viruses are postulated to subsequently deposit across the Southern US during lower zonal geostrophic winds each late Summer. This seasonally refreshed viral load is postulated to trigger a new influenza outbreak, once the existing IgE antibodies diminish to a critical value each Fall. Our study offers a new and consistent explanation for the seasonal diminishment of respiratory viral illnesses in temperate climates, the subdued seasonal signature in the tropics, the annually circulated virus phenotypes, and the northerly migration of influenza across the US every year. Our integrated geospatial and IgE hypothesis provides a new perspective for prediction, mitigation and prevention of the outbreak and spread of seasonal respiratory viruses including Covid-19 pandemic.


Asunto(s)
COVID-19/epidemiología , Brotes de Enfermedades/estadística & datos numéricos , Gripe Humana/epidemiología , Infecciones por Virus Sincitial Respiratorio/epidemiología , Enfermedades Respiratorias/epidemiología , SARS-CoV-2/fisiología , Antígenos de Plantas , Atmósfera , Humanos , Inmunoglobulina E/metabolismo , Pandemias , Polen , Estaciones del Año , Estados Unidos/epidemiología
4.
Front Immunol ; 12: 697074, 2021.
Artículo en Inglés | MEDLINE | ID: covidwho-1311376

RESUMEN

The development of a safe and effective vaccine against SARS-CoV-2, the causative agent of pandemic coronavirus disease-2019 (COVID-19), is a global priority. Here, we aim to develop novel SARS-CoV-2 vaccines based on a derivative of less commonly used rare adenovirus serotype AdC68 vector. Three vaccine candidates were constructed expressing either the full-length spike (AdC68-19S) or receptor-binding domain (RBD) with two different signal sequences (AdC68-19RBD and AdC68-19RBDs). Single-dose intramuscular immunization induced robust and sustained binding and neutralizing antibody responses in BALB/c mice up to 40 weeks after immunization, with AdC68-19S being superior to AdC68-19RBD and AdC68-19RBDs. Importantly, immunization with AdC68-19S induced protective immunity against high-dose challenge with live SARS-CoV-2 in a golden Syrian hamster model of SARS-CoV-2 infection. Vaccinated animals demonstrated dramatic decreases in viral RNA copies and infectious virus in the lungs, as well as reduced lung pathology compared to the control animals. Similar protective effects were also found in rhesus macaques. Taken together, these results confirm that AdC68-19S can induce protective immune responses in experimental animals, meriting further development toward a human vaccine against SARS-CoV-2.


Asunto(s)
Vacunas contra el Adenovirus/administración & dosificación , Vacunas contra la COVID-19/administración & dosificación , COVID-19/prevención & control , Esquemas de Inmunización , Inmunogenicidad Vacunal , SARS-CoV-2/inmunología , Vacunación/métodos , Vacunas contra el Adenovirus/inmunología , Animales , Anticuerpos Neutralizantes/inmunología , Anticuerpos Antivirales/inmunología , COVID-19/virología , Vacunas contra la COVID-19/inmunología , Cricetinae , Modelos Animales de Enfermedad , Femenino , Células HEK293 , Humanos , Masculino , Ratones , Ratones Endogámicos BALB C , Pan troglodytes , ARN Viral/sangre , Glicoproteína de la Espiga del Coronavirus/inmunología , Transfección , Resultado del Tratamiento
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