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1.
Viruses ; 14(11)2022 10 31.
Artigo em Inglês | MEDLINE | ID: mdl-36366517

RESUMO

Therapeutic blood products including convalescent plasma/serum and immunoglobulins concentrated from convalescent plasma, such as intravenous immunoglobulins or hyperimmune globulins, and monoclonal antibodies are passive immunotherapy options for novel coronavirus disease 2019 (COVID-19). They have been shown to improve the clinical status and biological and radiological parameters in some groups of COVID-19 patients. However, blood products are still potential sources of virus transmission in recipients. The use of pathogen reduction technology (PRT) should increase the safety of the products. The purpose of this study was to determine the impact of solvent/detergents (S/D) procedures on SARS-COV-2 infectivity elimination in the plasma of donors but also on COVID-19 convalescent serum (CCS) capacity to neutralize SARS-COV-2 infectivity. In this investigation, S/D treatment for all experiments was performed at a shortened process time (30 min). We first evaluated the impact of S/D treatments (1% TnBP/1% TritonX-45 and 1% TnBP/1% TritonX-100) on the inactivation of SARS-COV-2 pseudoparticles (SARS-COV-2pp)-spiked human plasma followed by S/D agent removal using a Sep-Pak Plus C18 cartridge. Both treatments were able to completely inactivate SARS-COV-2pp infectivity to an undetectable level. Moreover, the neutralizing activity of CCS against SARS-COV-2pp was preserved after S/D treatments. Our data suggested that viral inactivation methods using such S/D treatments could be useful in the implementation of viral inactivation/elimination processes of therapeutic blood products against SARS-COV-2.


Assuntos
COVID-19 , SARS-CoV-2 , Humanos , COVID-19/terapia , Inativação de Vírus , Imunização Passiva/métodos , Anticorpos Antivirais , Anticorpos Neutralizantes , Soroterapia para COVID-19
2.
Viruses ; 14(3)2022 03 11.
Artigo em Inglês | MEDLINE | ID: mdl-35336986

RESUMO

Since the 2014-2016 epidemic, Ebola virus (EBOV) has spread to several countries and has become a major threat to global health. EBOV is a risk group 4 pathogen, which imposes significant obstacles for the development of countermeasures against the virus. Efforts have been made to develop anti-EBOV immunization and therapeutics, with three vaccines and two antibody-based therapeutics approved in recent years. Nonetheless, the high fatality of Ebola virus disease highlights the need to continuously develop antiviral strategies for the future management of EBOV outbreaks in conjunction with vaccination programs. This review aims to highlight potential EBOV therapeutics and their target(s) of inhibition, serving as a summary of the literature to inform readers of the novel candidates available in the continued search for EBOV antivirals.


Assuntos
Vacinas contra Ebola , Ebolavirus , Epidemias , Doença pelo Vírus Ebola , Antivirais/farmacologia , Antivirais/uso terapêutico , Ebolavirus/fisiologia , Doença pelo Vírus Ebola/epidemiologia , Doença pelo Vírus Ebola/prevenção & controle , Humanos , Imunização
3.
Sci Rep ; 7: 41255, 2017 01 23.
Artigo em Inglês | MEDLINE | ID: mdl-28112264

RESUMO

The western honeybee (Apis mellifera) is essential for the global economy due to its important role in ecosystems and agriculture as a pollinator of numerous flowering plants and crops. Pesticide abuse has greatly impacted honeybees and caused tremendous loss of honeybee colonies worldwide. The reasons for colony loss remain unclear, but involvement of pesticides and pathogen-pesticide interactions has been hypothesized. Histone deacetylase inhibitors (HDACis) inhibit the activity of histone acetylase, which causes the hyperacetylation of histone cores and influences gene expression. In this study, sodium butyrate, an HDACi, was used as a dietary supplement for honeybees; after treatment, gene expression profiles were analyzed using quantitative PCR. The results showed that sodium butyrate up-regulated genes involved in anti-pathogen and detoxification pathways. The bioassay results showed that honeybees treated with sodium butyrate were more tolerant to imidacloprid. Additionally, sodium butyrate strengthened the immune response of honeybees to invasions of Nosema ceranae and viral infections. We also performed a bioassay in which honeybees were exposed to pesticides and pathogens. Our results provide additional data regarding the mechanism by which honeybees react to stress and the potential application of HDACis in beekeeping.


Assuntos
Abelhas/efeitos dos fármacos , Abelhas/genética , Regulação da Expressão Gênica/efeitos dos fármacos , Histonas/metabolismo , Transdução de Sinais/genética , Acetilação/efeitos dos fármacos , Animais , Peptídeos Catiônicos Antimicrobianos/farmacologia , Abelhas/imunologia , Abelhas/microbiologia , Ácido Butírico/farmacologia , Caspase 3/metabolismo , Inativação Metabólica/efeitos dos fármacos , Inativação Metabólica/genética , Microsporidiose/genética , Microsporidiose/patologia , Neonicotinoides/farmacologia , Nitrocompostos/farmacologia , Nosema/efeitos dos fármacos , Nosema/fisiologia , Transdução de Sinais/efeitos dos fármacos
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