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Med Sci Monit ; 27: e934365, 2021 Nov 19.
Artigo em Inglês | MEDLINE | ID: mdl-34795200

RESUMO

BACKGROUND Autologous blood-derived products can target specific inflammatory molecular pathways and have potentially beneficial therapeutic effects on inflammatory pathologies. The purpose of this study was to assess in vitro the anti-inflammatory and anti-catabolic potential of an autologous blood product as a possible treatment for COVID-19-induced cytokine storm. MATERIAL AND METHODS Blood samples from healthy donors and donors who had recovered from COVID-19 were incubated using different techniques and analyzed for the presence of anti-inflammatory, anti-catabolic, regenerative, pro-inflammatory, and procatabolic molecules. RESULTS The highest concentrations of therapeutic molecules for targeting inflammatory pathways were found in the blood that had been incubated for 24 h at 37°C, whereas a significant increase was observed after 6 h of incubation in blood from COVID-19-recovered donors. Beneficially, the 6-h incubation process did not downregulate anti-COVID-19 immunoglobulin G concentrations. Unfortunately, increases in matrix metalloproteinase 9, tumor necrosis factor alpha, and interleukin-1 were detected in the product after incubation; however, these increases could be blocked by adding citric acid, with no effect on the concentration of the target therapeutic molecules. Our data allow for safer and more effective future treatments. CONCLUSIONS An autologous blood-derived product containing anti-inflammatory and anti-catabolic molecules, which we term Cytorich, has a promising therapeutic role in the treatment of a virus-induced cytokine storm, including that associated with COVID-19.


Assuntos
Anabolizantes/sangue , Anti-Inflamatórios/sangue , COVID-19/complicações , Síndrome da Liberação de Citocina/tratamento farmacológico , Adulto , Anabolizantes/isolamento & purificação , Anabolizantes/uso terapêutico , Anti-Inflamatórios/isolamento & purificação , Anti-Inflamatórios/uso terapêutico , COVID-19/sangue , Síndrome da Liberação de Citocina/etiologia , Feminino , Humanos , Interleucina-1beta/antagonistas & inibidores , Masculino , Metaloproteinase 9 da Matriz/metabolismo , Metabolismo/efeitos dos fármacos , Pessoa de Meia-Idade , Adulto Jovem , Tratamento Farmacológico da COVID-19
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