Pedersen N C, Morris B
J Exp Med. 1970 May 1;131(5):936-69. doi: 10.1084/jem.131.5.936.
The rejection of renal homografts has been studied in sheep by transplanting kidneys into the neck and preserving the renal lymphatic drainage intact. Chronic fistulae were established in the transplanted renal lymphatics and lymph collected throughout the life of the graft. The changes that occurred in homografts during the process of rejection were reflected in changes in the lymph. Large numbers of basophilic, blast, lymphoid cells appeared in the lymph, and lymph production in the grafted kidney increased 20-50 fold. Over a period of about 10 days, up to 60 g wet weight of lymphoid cells and up to 10 liters of lymph were collected from the graft. Within 24 hr of grafting, the host cells present in the renal lymph had become sensitized to the graft and transformed into blast cells when cultivated in Millipore chambers in vitro. When the cells leaving the graft during the first 18-48 hr were injected into distant nonstimulated lymph nodes of the host sheep, they evoked significant cellular and antibody responses in the nodes. Within the graft, the main pathological changes were found in the vascular endothelium and many of the peritubular capillaries become plugged with emboli comprised of blast cells. There was extensive infiltration of the renal parenchyma with lymphoid cells and evidence of their transformation and proliferation within the renal blood capillaries. When all the lymph and cells leaving the homograft were diverted from the body, there was a greatly decreased reaction in the regional prescapular lymph node, and no reaction in lymph nodes distant from the graft. In these circumstances, the survival of the graft was not prolonged, and it was rejected without involvement of the lymph nodes of the host. Humoral antibody was produced in the lymph node regional to the homograft within 48-60 hr of grafting. Antibody was not detected in the blood or in the renal lymph until near to the time the graft was rejected. It was thought that this was due to the binding of antibody by the kidney graft tissue. We conclude that all the events which lead to the recognition and rejection of renal homografts can occur centrally within the graft itself.
通过将肾脏移植到颈部并保持肾淋巴引流完整,对绵羊同种异体肾移植排斥反应进行了研究。在移植的肾淋巴管中建立慢性瘘管,并在整个移植肾的存活期内收集淋巴液。排斥过程中同种异体移植肾发生的变化反映在淋巴液的变化中。淋巴液中出现大量嗜碱性、母细胞样、淋巴细胞,移植肾中的淋巴液生成增加了20至50倍。在大约10天的时间里,从移植肾中收集到高达60克湿重的淋巴细胞和多达10升的淋巴液。移植后24小时内,肾淋巴液中的宿主细胞对移植肾产生致敏作用,并在体外微孔小室中培养时转化为母细胞。当在最初18至48小时内离开移植肾的细胞被注射到宿主绵羊远处未受刺激的淋巴结中时,它们在淋巴结中引发了显著的细胞和抗体反应。在移植肾内,主要病理变化见于血管内皮,许多肾小管周围毛细血管被由母细胞组成的栓子堵塞。肾实质有广泛的淋巴细胞浸润,并有证据表明它们在肾血毛细血管内发生转化和增殖。当离开同种异体移植肾的所有淋巴液和细胞都从体内引流出去时,肩胛前区局部淋巴结的反应大大降低,远离移植肾的淋巴结则无反应。在这种情况下,移植肾的存活期并未延长,且在未累及宿主淋巴结的情况下被排斥。移植后48至60小时内,在同种异体移植肾局部的淋巴结中产生了体液抗体。直到接近移植肾被排斥时,才在血液或肾淋巴液中检测到抗体。据认为,这是由于抗体被肾移植组织结合所致。我们得出结论,导致同种异体肾移植被识别和排斥的所有事件都可在移植肾自身内部集中发生。