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CTLA-4Ig治疗C57BL/6小鼠自身免疫性肝炎的实验研究 被引量:3

Experimental investigation of cytotoxic T lymphocyte associated molecule-4 Ig in treatment of autoimmune hepatitis in C57BL/6 mice
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摘要 目的研究 CTL A- 4Ig在治疗 C5 7BL/ 6小鼠自身免疫性肝炎上的作用。方法通过用 C5 7BL/ 6近交系小鼠的肝特异性抗原与弗氏完全佐剂混合物免疫攻击小鼠 ,随后用 CTL A- 4Ig治疗 ,观察小鼠的临床经过、血生化、肝脏组织学改变。结果随着免疫次数的增多 ,治疗组临床经过、血生化、肝脏组织学改变逐步与正常对照组相似 ,而病理模型组与前两组有明显差异 :血生化可见天冬氨酸氨基转移酶、球蛋白显著升高 ;肝组织学检测可见炎细胞的浸润 ,肝细胞的肿胀、灶性坏死甚至广泛坏死 ;肝组织免疫荧光检测提示有大量免疫球蛋白沉着。结论 CTL A- 4Ig能有效地治疗 C5 7BL / ObjectiveTo investigate the role of cytotoxic T lymphocyte associated molecule 4Ig(CTLA 4Ig) in treatment autoimmune hepatitis in C57BL/6 mice Methods C57BL/6 mice were intraperitoneally immunized with C57BL/6 mice liver specific protein in complete Freund's adjuvant, CTLA 4Ig were subsequently given Clinical conditions, serum biochemistry alteration of liver histology of C57BL/6 mice were observed Results With sequential immunization, the clinical, serum biochemistry, liver histological changes in treated group were similar to those of the control group; In the pathological model group, aspartate aminotransferase and globulin significantly increased Inflammatory cell infiltration, hepatic cell swelling, focal necrosis and severe hepatocyte necrosis were found in liver; and liver immunofluorescence detection cued that there were many immunoglobulin deposited there, it is significantly different to the other two groups Conclusion CTLA 4Ig can treat C57BL/6 mice autoimmune hepatitis
出处 《免疫学杂志》 CAS CSCD 北大核心 2001年第6期453-456,共4页 Immunological Journal
基金 国家自然科学基金重点项目 (39993430 - 2 ) 国家自然科学基金面上项目 (39970 75 6 ) 国家科技部重点项目 (96 -92 0 - 2 0 - 10 ) 重庆市科委院士基金 (96 90 10 5 18)资助项目
关键词 CTLA-4IG 自身免疫性肝炎 免疫治疗 C57BL/6小鼠 CTLA 4Ig autoimmune hepatitis
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  • 1罗高兴,中华整形烧伤外科杂志,2000年,16卷,1期,37页 被引量:1
  • 2Chattopadhyay D,Indian J Pathol Microbiol,1999年,42卷,3期,291页 被引量:1
  • 3林学颜,现代细胞与分子免疫学,1999年,181页 被引量:1
  • 4中华内科杂志,1995年,34卷,11期,788页 被引量:1
  • 5Lohse A W,Heapatology,1990年,11卷,1期,24页 被引量:1
  • 6Manns M,Clin Exp Immunol,1980年,42卷,2期,263页 被引量:1

同被引文献25

  • 1Rossini AA, Mordes JP, Greiner DL, a 02. Islet cell transplantation tolerance [J]. Transplantation, 2001, 72(8 Suppl) :S43 - S46. 被引量:1
  • 2Ferguson J, Allsopp RH, Taylor RM, et al. Isolation and preservation of islets from the mouse, rat, guinea-pig and human pancreas [J]. Br J Surg, 1976,63(10) : 767 - 773. 被引量:1
  • 3Naldini L, Blomer U, Gallay P, et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector[J]. Science, 1996,272(5 259) : 263 - 267. 被引量:1
  • 4Ju Q, Edelstein D, Brendel MD, et al. Transduction of nondividing adult human pancreatic beta cells by an integrating lentiviral vector [J]. Diabetologia, 1998,41 (6) : 736 - 739. 被引量:1
  • 5Oberholzer J, Toso C, Ris F, et al. Beta cell replacement for the treatment of diabetes [J]. Ann N Y Acad Sci, 2001,944:373 - 387. 被引量:1
  • 6Judge TA, Tang A, Turka LA. Immunosuppression through blockade of CD28: B7-mediated costimulatory signals [J].Immunol Res, 1996,15( 1 ) : 38 - 49. 被引量:1
  • 7Gainer AL, Suarez Pinzon WL, Min WP, et al. Prolongation of allograft survival of transfected islets expressing human CTLA4-Ig, human soluble Fas ligand or a combination of the two[J]. Transplant Proc, 1998,30(2): 534. 被引量:1
  • 8Feng S, Quickel RR, Hollister Lock J, et al. Prolonged xenograft survival of islets infected with small doses of adenovirus expressing CILA4Ig [J]. Transplantation, 1999, 67 (12) :1 037-1 613. 被引量:1
  • 9Gallichan WS, Kafri T, Krahl T, et al. Lentivirus-mediated transduction of islet grafts with interleukin 4 results in sustained gene expression and protection from insuhtis [J]. Hum Gene Ther, 1998,9(18): 2 717-2 726. 被引量:1
  • 10Vitali C, Bombardieri S, Jonsson R ,et al. Classification criteria for sjogren' syndrome:A revised version of the Europeancriteria proposed by the American-European consensus group[J].Ann Rheum Dis ,2002,61(6):554-558. 被引量:1

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