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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Posttransplant lymphoproliferative disorder after liver transplantation in miniature swine.
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Posttransplant lymphoproliferative disorder after liver transplantation in miniature swine.

机译:小型猪肝移植后的移植后淋巴细胞增生性疾病。

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BACKGROUND: Posttransplant lymphoproliferative disorder (PTLD) is a well-known, life-threatening complication of immunosuppressive therapy, occurring in both adult and pediatric transplant recipients. METHODS: To study the effect of major histocompatibility complex on tolerance induction to primarily vascularized liver allograft, a semi-identical miniature swine model was developed to mimic the clinical situation of parent-into-infant liver transplantation. Long-term acceptance of semi-identical liver allograft was obtained by a transient course of FK506. In a subgroup of six animals, three developed a lethal PTLD. These animals were studied by histology and immunohistochemistry and the anti-donor cellular immune response was assessed. In addition, the possible viral origin of the proliferative process was evoked. RESULTS: Histology and immunohistochemistry revealed an abnormal B-cell proliferation in many organs of swine suffering from PTLD. Evidence of human Epstein-Barr virus, cytomegalovirus, and adenovirus was not evidenced, but a porcine virus responsible for a respiratory and reproductive syndrome (PRRS) was identified in the lymphoid tissue of these animals. In mixed lymphocyte reaction, a significant antiself immune response confirmed an infection by a virus. CONCLUSIONS: This is the first report suggesting that PRRS virus might provoke PTLD in immunosuppressed miniature swine after orthotopic liver transplantation. Whether PTLD could be induced by injection of the PRRS virus in immunosuppressed animals, a pig model of PTLD might be developed and would represent an interesting preclinical model for testing anti-PTLD therapies.
机译:背景:移植后淋巴组织增生性疾病(PTLD)是免疫抑制治疗的众所周知的威胁生命的并发症,在成人和小儿移植受者中均发生。方法:为研究主要组织相容性复合物对主要血管化同种异体肝移植耐受诱导的影响,建立了半相同的微型猪模型,以模拟母婴肝移植的临床情况。长期接受半同种异体肝移植是通过FK506的短暂过程获得的。在六只动物的亚组中,三只动物产生了致命的PTLD。通过组织学和免疫组织化学研究这些动物,并评估抗供体细胞免疫应答。另外,诱发了增殖过程的可能的病毒起源。结果:组织学和免疫组化显示,患有PTLD的猪许多器官中的B细胞增殖异常。尚无人类爱泼斯坦-巴尔病毒,巨细胞病毒和腺病毒的证据,但在这些动物的淋巴组织中发现了引起呼吸和生殖综合症(PRRS)的猪病毒。在混合淋巴细胞反应中,重要的抗自身免疫反应证实了病毒感染。结论:这是第一个报道,表明PRRS病毒可能在原位肝移植后免疫抑制的小型猪中激发PTLD。无论是否可以通过在免疫抑制动物中注射PRRS病毒来诱导PTLD,可能会开发出PTLD的猪模型,并将代表一个有趣的临床前模型来测试抗PTLD疗法。

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