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1.
Transpl Infect Dis ; 17(3): 456-62, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25850995

RESUMEN

Neurocysticercosis, an infection of the central nervous system with the larval stage of the cestode Taenia solium, is common in developing countries but its occurrence and management in allogeneic hematopoietic stem cell transplantation (HSCT) has not been reported previously, to our knowledge. We report the case of an immigrant female patient who underwent a matched-related allogeneic HSCT for acute lymphoblastic leukemia and was incidentally found to have a solitary viable neurocysticercosis lesion. However, despite severe immunosuppression, the size of the cyst did not increase. More importantly, restoration of the immune system did not induce significant inflammation or seizures. Subsequent follow-up demonstrated complete resolution of the neurocysticercosis lesion. Thus, in the setting of HSCT, an asymptomatic patient with a single neurocysticercosis lesion was successfully managed without the use of anthelmintics, steroids, or anti-epileptics.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas/efectos adversos , Neurocisticercosis/complicaciones , Leucemia-Linfoma Linfoblástico de Células Precursoras/complicaciones , Adulto , Quistes , Femenino , Humanos , Terapia de Inmunosupresión , Neurocisticercosis/terapia , Leucemia-Linfoma Linfoblástico de Células Precursoras/cirugía , Trasplante Homólogo
2.
Sci Rep ; 11(1): 9591, 2021 05 05.
Artículo en Inglés | MEDLINE | ID: mdl-33953282

RESUMEN

Three commercial powders of MgB2 were tested in vitro by MTS and LDH cytotoxicity tests on the HS27 dermal cell line. Depending on powders, the toxicity concentrations were established in the range of 8.3-33.2 µg/ml. The powder with the lowest toxicity limit was embedded into polyvinylpyrrolidone (PVP), a biocompatible and biodegradable polymer, for two different concentrations. The self-replenishing MgB2-PVP composite materials were coated on substrate materials (plastic foil of the reservoir and silicon tubes) composing a commercial urinary catheter. The influence of the PVP-reference and MgB2-PVP novel coatings on the bacterial growth of Staphylococcus aureus ATCC 25923, Enterococcus faecium DMS 13590, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, in planktonic and biofilm state was assessed in vitro at 6, 24, and 48 h of incubation time. The MgB2-PVP coatings are efficient both against planktonic microbes and microbial biofilms. Results open promising applications for the use of MgB2 in the design of anti-infective strategies for different biomedical devices and systems.


Asunto(s)
Antibacterianos/farmacología , Dermis/efectos de los fármacos , Línea Celular , Materiales Biocompatibles Revestidos/farmacología , Enterococcus faecalis/efectos de los fármacos , Enterococcus faecalis/crecimiento & desarrollo , Escherichia coli/efectos de los fármacos , Escherichia coli/crecimiento & desarrollo , Humanos , Povidona/farmacología , Pseudomonas aeruginosa/efectos de los fármacos , Pseudomonas aeruginosa/crecimiento & desarrollo , Staphylococcus aureus/efectos de los fármacos , Staphylococcus aureus/crecimiento & desarrollo
3.
Rom J Intern Med ; 37(1): 81-9, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-15523948

RESUMEN

The aim of this study is to show the intracellular Ca2+ changes induced by methotrexate, a cell cycle inhibitor, in order to prove the intracellular Ca2+ implication in cell proliferation processes. The fluorescent dye used to measure this parameter is Fluo-3, a fluorescein derivative useful for measuring the kinetics of Ca2+ transitions, waves and oscillations. The alterations of Ca2+ concentration proper to K562 cells have been studied, using methotrexate as a cell activation factor, both as direct effects on the cell response (1-15 minutes), and effects in time (24h.), using methotrexate in the culture medium. The K562 response at Ca2+ level in time remained constant for the cells grown in methotrexate medium, showing a slight increase in the control medium. We proved that methotrexate, a cell cycle inhibitor decreased the cytoplasmatic Ca2+ concentration in K562 cells, soon after adding methotrexate both to T0 and T1.


Asunto(s)
Calcio/metabolismo , Citoplasma/metabolismo , Compuestos de Anilina , Ciclo Celular/efectos de los fármacos , División Celular/fisiología , Citometría de Flujo , Colorantes Fluorescentes , Humanos , Células K562 , Metotrexato/farmacología , Xantenos
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