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Bases moleculares del defecto opsónico en niños inmunodeficientes
1Department of Medicine, St. Mary's Hospital Medical School, London, UK.
Los bajos niveles de proteína de unión a la manosa (MBP), vinculados a infecciones recurrentes, se derivan de una mutación genética específica. Este rasgo autosómico dominante interrumpe el MBP.
Área de la Ciencia:
- Inmunología Inmunología.
- Genética La genética.
Sus antecedentes:
- La proteína de unión a la manosa (MBP) juega un papel crucial en el sistema inmunológico innato como una opsonina.
- Las bajas concentraciones séricas de MBP están asociadas con un defecto opsónico, aumentando la susceptibilidad a las infecciones.
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