摘要
[目的]探讨建立具有人免疫学特征的卵巢癌-SCID鼠模型的可行性。[方法]将16只雌性SCID小鼠随机分为4组。A组:磷酸盐缓冲液(PBS)0.5ml;B组为荷HO-8910组:HO-8910细胞1×106个/只;C组为人免疫重建组:PBL细胞4×107个/只,进行免疫重建;D组为荷HO-8910免疫重建组:PBL细胞4×107个/只,24h后腹腔注射HO-8910细胞1×106个/只,观察各组小鼠的生物学及免疫学特性。[结果]免疫重建鼠的骨髓、肝脏、脾脏、胸腺、淋巴结、外周血、腹腔液中检测到人源性细胞;荷HO-8910细胞免疫重建组小鼠移植瘤体积小于荷HO-8910组小鼠;各组均无移植物抗宿主病(GVHD)发生。[结论]初步建立免疫重建荷人卵巢癌-SCID鼠模型,为卵巢癌治疗的临床前研究提供了理想动物模型。
[Purpose]To investigate the feasibility of establish a human ovarian carcinoma model in human lymphocyte-engrafted to severe combined immunodeficient (hu-PBL-SCID) mice. [Methods]Sixteen SCID mice were randomly divided into 4 groups: group A with intraperitoneally phosphate buffered saling (0.5ml each mouse), group B with human ovarian carcinoma cells HO-8910(1×10^6 each mouse), group C with human peripheral blood lymphocyte (PBL) (4×10^7 each mouse) for immune reconstruction, and group D with PBL (4×10^7 each mouse) and HO-8970 (1×10^6 each mouse) cells. The biological and immunological features of each groups were evaluated. [Results]Human immunological cells were detected in bone marrow, liver, spleen, thymus, lymphoid mode, peripheral blood and peritoneal fluid of hu-PBL-SCID mice. The volume of tumor were less in the reconstruction of human immunsystem group. No graft-versus-host disease (GVHD) was found in all groups. [Conclusion]A human ovarian carcinoma model has been established in hu-PBL-SCID mice which is an ideal animal model for preclinical research and treatment for ovarian carcinoma.
出处
《中国肿瘤》
CAS
2006年第8期558-560,共3页
China Cancer
基金
安徽省自然科学基金资助项目(20050430701)
安徽省自然科学基金资助项目(03043703)
安徽省教育厅自然科学研究计划项目(2005KJ256)