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药物诱导的小鼠同种异体移植耐受。IX. 通过从对H-2相同受体产生耐受的供体进行同种异体脾细胞移植建立完全嵌合状态。

Drug-induced tolerance to allografts in mice. IX. Establishment of complete chimerism by allogeneic spleen cell transplantation from donors made tolerant to H-2-identical recipients.

作者信息

Mayumi H, Himeno K, Tanaka K, Tokuda N, Fan J L, Nomoto K

出版信息

Transplantation. 1986 Oct;42(4):417-22.

PMID:3532453
Abstract

Graft-versus-host reaction (GVH) after allogeneic spleen cell transplantation was completely suppressed in an H-2-matched murine combination (AKR/J Sea [H-2k]----lethally irradiated C3H/He Slc [H-2k]) by pretreatment of the donors with recipient spleen cell antigen plus cyclophosphamide (CP). Irradiated recipients receiving cells became chimeric. In contrast to the H-2 matched combination, lethal GVH reaction could not be prevented in an H-2-mismatched fully allogeneic combination (C57BL/6 Cr Slc [H-2b]----lethally irradiated C3H/He Slc [H-2k]) by pretreatment of the donors. The results suggest that the effectors responsible for the GVH reaction were abrogated by pretreatment of the donors with allogeneic recipient spleen cells plus CP in the H-2-matched combination, but donor pretreatment failed to abrogate GVH reaction in the H-2-mismatched combination.

摘要

在同基因脾细胞移植后发生的移植物抗宿主反应(GVH),在一个H-2匹配的小鼠组合(AKR/J Sea [H-2k]→经致死剂量照射的C3H/He Slc [H-2k])中,通过用受体脾细胞抗原加环磷酰胺(CP)预处理供体而被完全抑制。接受细胞的受照射受体变成了嵌合体。与H-2匹配组合相反,在一个H-2不匹配的完全异基因组合(C57BL/6 Cr Slc [H-2b]→经致死剂量照射的C3H/He Slc [H-2k])中,供体的预处理不能预防致死性GVH反应。结果表明,在H-2匹配组合中,用异基因受体脾细胞加CP预处理供体可消除负责GVH反应的效应细胞,但在H-2不匹配组合中,供体预处理未能消除GVH反应。

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1
Drug-induced tolerance to allografts in mice. IX. Establishment of complete chimerism by allogeneic spleen cell transplantation from donors made tolerant to H-2-identical recipients.药物诱导的小鼠同种异体移植耐受。IX. 通过从对H-2相同受体产生耐受的供体进行同种异体脾细胞移植建立完全嵌合状态。
Transplantation. 1986 Oct;42(4):417-22.
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引用本文的文献

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Bone Marrow Transplant. 2023 Nov;58(11):1215-1222. doi: 10.1038/s41409-023-02085-2. Epub 2023 Aug 18.
2
A Review of Cyclophosphamide-Induced Transplantation Tolerance in Mice and Its Relationship With the HLA-Haploidentical Bone Marrow Transplantation/Post-Transplantation Cyclophosphamide Platform.环磷酰胺诱导的小鼠移植耐受及其与 HLA 单倍体相合骨髓移植/移植后环磷酰胺平台的关系研究综述。
Front Immunol. 2021 Sep 29;12:744430. doi: 10.3389/fimmu.2021.744430. eCollection 2021.
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Mechanisms of Graft-versus-Host Disease Prevention by Post-transplantation Cyclophosphamide: An Evolving Understanding.
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Front Immunol. 2019 Nov 29;10:2668. doi: 10.3389/fimmu.2019.02668. eCollection 2019.
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Novel regulatory therapies for prevention of Graft-versus-host disease.防治移植物抗宿主病的新型调节疗法。
BMC Med. 2012 May 15;10:48. doi: 10.1186/1741-7015-10-48.
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Innate and adaptive immune responses are tolerized in chimeras prepared with nonmyeloablative conditioning.在非清髓性条件下制备的嵌合体中,先天和适应性免疫反应被耐受化。
Transplantation. 2012 Mar 15;93(5):469-76. doi: 10.1097/TP.0b013e318242bddf.
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Efficacy and limitations of natural killer cell depletion in cyclophosphamide-induced tolerance.环磷酰胺诱导耐受中自然杀伤细胞耗竭的疗效与局限性
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Induction of classical transplantation tolerance in the adult.在成年个体中诱导经典移植耐受。
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