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CTLA4-Ig在器官移植术后免疫排斥反应中的应用 被引量:1

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摘要 CTLA4Ig是一种新型、高效的免疫抑制剂 ,主要通过竞争性抑制CD2 8与B7的结合来阻止共刺激信号的传递 ,抑制抗原特异性T淋巴细胞的增殖活化 ,未达到抑制免疫反应及诱导免疫耐受的作用 ,且无明显的毒副作用 ,因而在器官和组织移植排斥的防治和一些难治性自身免疫性疾病的治疗中有着广阔的应用前景。
作者 牛晓光
出处 《国外医学(免疫学分册)》 2003年第1期33-36,共4页 Foreign Medical Sciences(Section of Immunology Foreign Medical Sciences)
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同被引文献27

  • 1金永柱,王光明,李爱玲,谢蜀生.腺病毒介导CTLA4-FasL基因转移诱导大鼠心脏移植物长期存活的作用[J].中华医学杂志,2003,83(22):1968-1974. 被引量:11
  • 2Ariyan C, Salvalaggio P, Fecteau S, et al. Cutting edge: Transplantation tolerance through enhanced CTLA4 expression [J]. J Immunol, 2003;171(11):5673-5677.
  • 3Najafian N,Sayegh MH. CTLA4-Ig: A novel immunosuppressive agent [J]. Expert Opin Investig Drugs, 2000;9(9):2147-2157.
  • 4Nabeyama K, Yasunami Y, Toyofuku A, et al.Beneficial effects of costimulatory blockade with anti-inducible costimulator antibody in conjunction with CTLA4-Ig on prevention of islet xenograft rejection from rat to mouse [J]. Transplantation, 2004;78(11):1590-1596.
  • 5Kita Y, Li XK, Ohba M, et al. Prolonged cardiac allograft survival in rats systemically injected adenoviral vectors containing CTLA4-Ig gene [J]. Transplantation, 1999;68(6):758-766.
  • 6Lu L,Gambotto A, Lee WC, et al. Adenoviral delivery of CTLA4-Ig into myeloid dendritic cells promotes their in vitro tolerogenicity and survival in allogeneic recipients [J]. Gene Ther, 1999;6(4):554-563.
  • 7Wang Q, Zhang M, Ding G, et al. Anti-ICAM-1 antibody and CTLA-4Ig synergistically enhance immature dendritic cells to induce donor-specific immune tolerance in vivo[J]. Immunol Lett, 2003;90(1):33-42.
  • 8Lenschow DL, Zeng Y, Thistlethwaite JR, et al. Long-term survival of xenogeneic pancreatic islet grafts induced by CTLA4lg[J]. Sciences,1992;257(5071):789-792.
  • 9Miao G, Ito T, Uchikoshi F, et al. Development of donor-specific immunoregulatory T-cells after local CTLA4-Ig gene transfer to pancreatic allograft [J]. Transplantation, 2004;78(1):59-64.
  • 10Yasunaga S, Tsukui T, Masuda K,et al. CTLA4 recombinant protein genetically fused to canine Fcepsilon receptor Ialpha enhances allergen specific lymphocyte responses in experimentally sensitized dogs [J]. J Vet Med Sci, 2004;66(6):611-617.

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