Sandhu J S, Gorczynski R, Shpitz B, Gallinger S, Nguyen H P, Hozumi N
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Transplantation. 1995 Jul 27;60(2):179-84.
Despite previous attempts there is currently no suitable animal model available for xenogeneic graft versus host disease (XGVHD) mediated via human immunocompetent cells. Recently, we have developed an efficient protocol to engraft SCID mice with human peripheral blood lymphocytes (Hu-PBLs). The engraftment efficiency is extremely high, such that 100% of Hu-PBL-SCID mice die of XGVHD within 4 weeks after engraftment with Hu-PBLs (3-5 x 10(7) cells). A series of experiments was performed to investigate the mechanisms involved in the severe XGVHD. The results suggest that XGVHD was induced by human CD4+ T cells, antixenogeneic (antimouse) antibodies, and lymphokines. The SCID mouse model will be extremely valuable for the evaluation and development of immunosuppressive agents and transplantation protocols for human XGVHD.
尽管此前曾进行过尝试,但目前尚无适用于由具有免疫活性的人类细胞介导的异种移植物抗宿主病(XGVHD)的动物模型。最近,我们开发了一种有效的方案,将人类外周血淋巴细胞(Hu-PBLs)移植到SCID小鼠体内。移植效率极高,以至于在移植Hu-PBLs(3-5×10⁷个细胞)后4周内,100%的Hu-PBL-SCID小鼠死于XGVHD。我们进行了一系列实验来研究严重XGVHD所涉及的机制。结果表明,XGVHD是由人类CD4⁺T细胞、抗异种(抗小鼠)抗体和淋巴因子诱导的。SCID小鼠模型对于评估和开发用于人类XGVHD的免疫抑制剂及移植方案将具有极其重要的价值。