Amiloidosis de Inmunoglobulinas: Diagnóstico, Tratamiento y Fisicoquímica

Palabras clave: fibras amiloides, inmunoglobulinas, amiloidogénesis, sistema de órganos

Resumen

Las amiloidosis de inmunoglobulinas son enfermedades ocasionadas por los fragmentos insolubles de las inmunoglobulinas que se depositan en diversos tejidos formando fibras amiloides; esta acumulación anormal de proteínas produce disfunción orgánica y eventualmente la muerte. Esta patología se divide en 2 tipos: la amiloidosis AL y la amiloidosis AH, la primera es la forma sistémica más frecuente, donde los amiloides derivan de fragmentos de las cadenas ligeras de las inmunoglobulinas; la segunda es menos frecuente y resulta de la deposición de fragmentos de las cadenas pesadas. Determinar si son fragmentos de la cadena ligera o pesada es importante para el pronóstico y el tratamiento. En esta revisión se abordan los procesos termodinámicos y cinéticos que conducen a la agregación de estas proteínas así como las patologías, sus diagnósticos y tratamientos.

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Publicado
2023-12-13
Cómo citar
Rodríguez López , M. A., Contreras, J. G., & Vázquez Contreras, E. (2023). Amiloidosis de Inmunoglobulinas: Diagnóstico, Tratamiento y Fisicoquímica. Ciencia Latina Revista Científica Multidisciplinar, 7(6), 599-613. https://doi.org/10.37811/cl_rcm.v7i6.8713
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