Hodgson H J
Scand J Gastroenterol Suppl. 1985;114:39-44. doi: 10.3109/00365528509093766.
Recent experimental work in rodents has demonstrated that the liver can function as an 'IgA-pump', transporting polymeric IgA from serum to bile via a secretory-component mediated uptake at the surface of the hepatic parenchymal cell. Studies are surveyed which indicate that, although this process occurs in man, it is to a strikingly lesser degree, and interruption of this pathway does not explain the high serum IgA levels often seen in chronic liver disease: the explanation for this lies in enhanced synthesis of IgA, and diminished polymeric IgA catabolism unrelated to hepatobiliary transport.
近期在啮齿动物身上进行的实验研究表明,肝脏可充当“IgA泵”,通过肝实质细胞表面的分泌成分介导摄取,将聚合IgA从血清转运至胆汁。现综述多项研究,这些研究表明,尽管此过程在人类中也会发生,但其程度明显较轻,而且该途径的中断并不能解释慢性肝病中常见的高血清IgA水平:其原因在于IgA合成增加,以及与肝胆转运无关的聚合IgA分解代谢减少。