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1.
Antioxidants (Basel) ; 9(10)2020 Sep 29.
Artigo em Inglês | MEDLINE | ID: mdl-33003552

RESUMO

Since the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) outbreak emerged, countless efforts are being made worldwide to understand the molecular mechanisms underlying the coronavirus disease 2019 (COVID-19) in an attempt to identify the specific clinical characteristics of critically ill COVID-19 patients involved in its pathogenesis and provide therapeutic alternatives to minimize COVID-19 severity. Recently, COVID-19 has been closely related to sepsis, which suggests that most deceases in intensive care units (ICU) may be a direct consequence of SARS-CoV-2 infection-induced sepsis. Understanding oxidative stress and the molecular inflammation mechanisms contributing to COVID-19 progression to severe phenotypes such as sepsis is a current clinical need in the effort to improve therapies in SARS-CoV-2 infected patients. This article aims to review the molecular pathogenesis of SARS-CoV-2 and its relationship with oxidative stress and inflammation, which can contribute to sepsis progression. We also provide an overview of potential antioxidant therapies and active clinical trials that might prevent disease progression or reduce its severity.

2.
Crit Care Med ; 48(12): 1841-1844, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-32826431

RESUMO

Great efforts are being made worldwide to identify the specific clinical characteristics of infected critically ill patients that mediate the associated pathogenesis, including vascular dysfunction, thrombosis, dysregulated inflammation, and respiratory complications. Recently, coronavirus disease 2019 has been closely related to sepsis, which suggests that most deaths in ICUs in infected patients are produced by viral sepsis. Understanding the physiopathology of the disease that lead to sepsis after severe acute respiratory syndrome coronavirus 2 infection is a current clinical need to improve intensive care-applied therapies applied to critically ill patients. Although the whole representative data characterizing the immune and inflammatory status in coronavirus disease 2019 patients are not completely known, it is clear that hyperinflammation and coagulopathy contribute to disease severity. Here, we present some common features shared by severe coronavirus disease 2019 patients and sepsis and describe proposed anti-inflammatory therapies for coronavirus disease 2019 which have been previously evaluated in sepsis.


Assuntos
COVID-19/imunologia , Cuidados Críticos/métodos , Síndrome do Desconforto Respiratório/imunologia , Sepse/imunologia , Anti-Inflamatórios/uso terapêutico , Transtornos da Coagulação Sanguínea/prevenção & controle , COVID-19/complicações , Citocinas/antagonistas & inibidores , Glucocorticoides/uso terapêutico , Humanos , Síndrome do Desconforto Respiratório/etiologia , SARS-CoV-2 , Sepse/etiologia , Sepse/terapia , Trombose
3.
Epigenomics ; 12(7): 617-646, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-32396480

RESUMO

Sepsis is a life-threatening condition that occurs when the body responds to an infection damaging its own tissues. Sepsis survivors sometimes suffer from immunosuppression increasing the risk of death. To our best knowledge, there is no 'gold standard' for defining immunosuppression except for a composite clinical end point. As the immune system is exposed to epigenetic changes during and after sepsis, research that focuses on identifying new biomarkers to detect septic patients with immunoparalysis could offer new epigenetic-based strategies to predict short- and long-term pathological events related to this life-threatening state. This review describes the most relevant epigenetic mechanisms underlying alterations in the innate and adaptive immune responses described in sepsis and septic shock, and their consequences for immunosuppression states, providing several candidates to become epigenetic biomarkers that could improve sepsis management and help predict immunosuppression in postseptic patients.


Assuntos
Epigênese Genética , Terapia de Imunossupressão , Sepse/genética , Choque Séptico/genética , Imunidade Adaptativa , Biomarcadores , Metilação de DNA , Histonas , Humanos , Imunidade Inata , RNA não Traduzido , Sepse/imunologia , Choque Séptico/imunologia
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