Elena Pascual

Dr. Elena Pascual


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
21 November 2017 in Veterinary Research
Verified
Journal Article
Open access
PDF file
JRJosé Manuel Rojas
José Manuel Rojas
MAMiguel Avia
Miguel Avia
EPElena Pascual
Elena Pascual
NSNoemí Sevilla
Noemí Sevilla
VMVerónica Martín
Verónica Martín
Peste des petits ruminants virus (PPRV) causes an economically important disease that limits productivity in small domestic ruminants and often affects the livestock of the poorest populations in developing countries. Animals that survive PPRV develop strong cellular and humoral responses, which are probably necessary for protection. Vaccination should thus aim at mimicking these natural responses. Immunization strategies against this morbillivirus using recombinant adenoviruses expressing PPRV-F or -H proteins can protect PPRV-challenged animals and permit differentiation of infected from vaccinated animals. Little is known of the T cell repertoire these recombinant vaccines induce. In the present work, we identified several CD4+ and CD8+ T cell epitopes in sheep infected with PPRV. We also show that recombinant adenovirus vaccination induced T cell responses to the same epitopes, and led to memory T cell differentiation. T cells primed by these recombinant adenovirus vaccines expanded after PPRV challenge and probably contributed to protection. These data validate the use of recombinant adenovirus expressing PPRV genes as DIVA strategies to control this highly contagious disease.

20 June 2023 in Molecules
Verified
Journal Article
Open access
PDF file
Alejandro CenalmorAlejandro Cenalmor
Alejandro Cenalmor
EPElena Pascual
Elena Pascual
SGSergio Gil-Manso
Sergio Gil-Manso
RCRafael Correa-Rocha
Rafael Correa-Rocha
JÁJosé Ramón Suárez Álvarez
José Ramón Suárez Álvarez
IAISABEL GARCIA ALVAREZ
ISABEL GARCIA ALVAREZ
Neuroinflammation plays a crucial role in the progression of Alzheimer’s disease and other neurodegenerative disorders. Overactivated microglia cause neurotoxicity and prolong the inflammatory response in many neuropathologies. In this study, we have synthesised a series of isatin derivatives to evaluate their anti-neuroinflammatory potential using lipopolysaccharide activated microglia as a cell model. We explored four different substitutions of the isatin moiety by testing their anti-neuroinflammatory activity on BV2 microglia cells. Based on the low cytotoxicity and the activity in reducing the release of nitric oxide, pro-inflammatory interleukin 6 and tumour necrosis factor α by microglial cells, the N1-alkylated compound 10 and the chlorinated 20 showed the best results at 25 µM. Taken together, the data suggest that 10 and 20 are promising lead compounds for developing new neuroprotective agents.