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Heart preservation and immunological tolerance induction in orthotopic heart transplantation in swines.

Heart preservation and immunological tolerance induction in orthotopic heart transplantation in swines.
猪原位心脏移植中的心脏保存和免疫耐受诱导。
批准号:
03454335
负责人:
YASUI Hisataka
金额:
$0.64万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1991
资助国家:
日本
项目状态:
已结题
起止时间:
1991 至 1992

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中文摘要
翻译
在各种全异基因小鼠组合中进一步研究环磷酰胺诱导的免疫耐受,同时尝试通过体外循环在猪体内建立原位心脏移植系统。给受体小鼠静脉注射100µg抗Thy 1.2单抗。第1,9×10^7全异基因脾细胞+3×10^7骨狭窄细胞静脉注射。第0天,环磷酰胺200 mg/kg,第2天,在不同的完全同种异体小鼠组合中,如C3H(H-2^k)*B6(H-2^b)、B6*C3H、BALB(H-2^d)*B6和BALB*C3H,诱导对耐受株的长期皮肤移植耐受。中位生存期分别为123天(n=19)、136天(n=9)、503天(n=15)和165天(n=8)。选用母猪(20-25公斤)。采用体外循环进行原位心脏移植。供心用九州大学停搏液(CP;Na87,K20)停搏,然后用CP或Collins‘s液(C;Na10,K117)冲洗并露出。保存温度为0゚C,保存4h。升主动脉开放后1小时,测定Emax。每组5头猪。CP组有3例(60%)和C组有1例(20%)能够停止体外循环。CP组3例中只有1例可进行Emax检查。LOS和出血是主要并发症。目前还没有找到任何长期幸存者。
英文摘要
Cyclophosphamide-induced immunological tolerance was further studied in various fully allogeneic murine combination, while a system of orthotopic heart transplantation was tried to established in swines by using cardiopulmonary bypass.Exp.1. When a recipient mouse was given 100mug anti Thy 1.2mAb i.v. on day-1,9x10^7 fully allogeneic spleen cells plus 3x10^7 bone narrow cells i.v. on day 0, and 200mg/kg cyclophosphamide on day 2, a long-lasting skin graft tolerance to the tolerogenic strain was induced in various fully allogeneic murine combinations such as C3H(H-2^k)*B6(H-2^b), B6*C3H, BALB(H-2^d)*B6, and BALB*C3H. The median survival (days) was 123 (n=19), 136(n=9), >503(n=15), and >165(n=8), respectively.Exp.2. Female swines (20-25kg) were used. Orthotopic heart transplantation was per-formed using cardiopulmonary bypass. The donor heart was arrested with Kyushu University cardioplegic solution (CP;Na87,K20)and then flushed with and emerged in the CP or in Collins' solution (C;Na10,K117). The preservation was performed at 0゚C for 4 hours. One hour after the aortic declamping, Emax was examined. Each group contained 5 pigs. Cardiopulmonary bypass was able to discontinue in 3(60%) in the CP group and in 1(20%) in the C group. Only one of the 3 of the CP group could be examined for Emax. LOS and bleeding was the major complications. Any long-term survivors were not obtained.
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Establishment of drug-induced tolerance for heart transplantation in large animals
  • 批准号:
    12470242
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 资助金额:
    $9.15万
  • 财政年份:
    2000
  • 负责人:
    YASUI Hisataka
  • 依托单位:
Modefication of the drug-induced tolerance induction to large animals
  • 批准号:
    10470277
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 资助金额:
    $8.06万
  • 财政年份:
    1998
  • 负责人:
    YASUI Hisataka
  • 依托单位:
Analysis of immunological mechanism and inhibition of post-transplant coronary artery disease in mice.
  • 批准号:
    08457304
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 资助金额:
    $4.1万
  • 财政年份:
    1996
  • 负责人:
    YASUI Hisataka
  • 依托单位:
国内基金
海外基金
Consequences of MALT1 mutation for B cell tolerance
  • 批准号:
    32100719
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    James Qun Wang
  • 依托单位: