Altorfer J, Huling S L, Jones A L
Abteilung für Gastroenterologie, Inselspital Bern.
Schweiz Med Wochenschr. 1988 May 21;118(20):769-72.
After intestinal priming with cholera toxin (CT) the highest number of specific B-cells is found in the liver, whereas after an intestinal booster dose of CT, high numbers of specific B-cells also locate to the intestine. Correspondingly, after priming, 70% of biliary IgA anti-CT are synthesized within the liver and after boosting approximately 30%. To test the hypothesis that the B-cells in the liver are derived from intestinal lymphoid tissue, thoracic duct lymphocytes (TDL) from intestinally primed and boosted donor rats were transferred to syngeneic recipients. TDL from primed donors predominantly homed to the liver of recipients, and TDL from boosted donors in high numbers to the intestine also. High biliary IgA anti-CT titers in both groups of recipients proved that the immune response was transmitted successfully. In the rat, at any rate, the liver is part of the intestinal immune system not only in terms of IgA transport but also as a specific homing organ for intestinal B-cells.
在用霍乱毒素(CT)进行肠道致敏后,肝脏中发现的特异性B细胞数量最多,而在用CT进行肠道加强剂量后,大量特异性B细胞也定位于肠道。相应地,致敏后,70%的胆汁IgA抗CT在肝脏内合成,加强后约为30%。为了验证肝脏中的B细胞来源于肠道淋巴组织这一假设,将来自经肠道致敏和加强的供体大鼠的胸导管淋巴细胞(TDL)转移到同基因受体中。来自致敏供体的TDL主要归巢到受体的肝脏,来自加强供体的TDL也大量归巢到肠道。两组受体中高胆汁IgA抗CT滴度证明免疫反应成功传递。无论如何,在大鼠中,肝脏不仅在IgA运输方面,而且作为肠道B细胞的特异性归巢器官,都是肠道免疫系统的一部分。