Orlans E, Peppard J, Reynolds J, Hall J
J Exp Med. 1978 Feb 1;147(2):588-92. doi: 10.1084/jem.147.2.588.
Immunoglobulins were isolated from the serum or ascitic fluid of Lou/Wsl rats bearing plasmacytomas and labeled with 125I. When labeled IgA was injected i.v. it disappeared from the blood serum much more rapidly than IgG2 so that after 3 h less than 10% remained. This rapid disappearance of the injected IgA was not seen in rats with ligated bile ducts. In rats with cannulated bile ducts, the labeled IgA appeared rapidly in the bile so that 25% of the injected dose was recovered in 3 h; at the peak of this biliary excretion the specific radioactivity of the bile (cpm/milligram protein) was about 200 times greater than that of the blood serum. Thus much of the IgA which finds its way into the blood is rapidly and actively transported across the liver so that it enters the gut lumen via the biliary tract.
从患有浆细胞瘤的Lou/Wsl大鼠的血清或腹水中分离出免疫球蛋白,并用125I进行标记。静脉注射标记的IgA后,它从血清中消失的速度比IgG2快得多,以至于3小时后剩余不到10%。在胆管结扎的大鼠中未观察到注射的IgA如此迅速地消失。在胆管插管的大鼠中,标记的IgA迅速出现在胆汁中,以至于在3小时内回收了25%的注射剂量;在这种胆汁排泄的高峰期,胆汁的比放射性(每分钟计数/毫克蛋白质)比血清高约200倍。因此,进入血液的许多IgA迅速且主动地通过肝脏转运,从而通过胆道进入肠腔。