2005, Número 2
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Rev Gastroenterol Mex 2005; 70 (2)
Vectores virales en terapia génica. Ventajas de los vectores adenoasociados
Sandoval RAS, Salazar MAM, Armendáriz-Borunda J
Idioma: Español
Referencias bibliográficas: 57
Paginas: 192-202
Archivo PDF: 73.89 Kb.
RESUMEN
La terapia génica se ha visto favorecida por el desarrollo de un número cada vez mayor de vectores, con el fin de lograr una expresión más persistente y una administración inocua. Dentro de los vectores virales los adenoasociados presentan ventajas prometedoras. Este virus de ADN es capaz de transducir gran variedad de líneas celulares, integrarse al genoma del huésped y lograr expresiones persistentes del transgén por lapso de meses, todo esto sin generar una respuesta inmune celular. La aplicación de nuevas metodologías en la producción y purificación de estos vectores ha mejorado considerablemente la cantidad y calidad de partículas infecciosas que se generan. En este momento, gracias a los mencionados desarrollos biotecnológicos, la terapia génica es una opción terapéutica viable para varias enfermedades crónico-degenerativas.
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