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在DBA/2小鼠中诱导同基因移植物抗宿主病样综合征。

Induction of a syngeneic graft-versus-host disease-like syndrome in DBA/2 mice.

作者信息

Bryson J S, Jennings C D, Caywood B E, Kaplan A M

机构信息

Department of Microbiology/Immunology, College of Medicine, University of Kentucky, Lexington 40536-0084.

出版信息

Transplantation. 1989 Dec;48(6):1042-7. doi: 10.1097/00007890-198912000-00030.

Abstract

Syngeneic graft-versus-host disease has been shown to occur in syngeneic rat radiation chimeras after treatment with a short course of CsA. However, data concerning this model have been controversial in murine systems. We have successfully induced a GVHD-like syndrome in syngeneic mouse radiation chimeras treated transiently with CsA. Lethally irradiated (950 rads) DBA/2 mice were reconstituted with syngeneic bone marrow and treated daily, i.p. with 15 mg/kg CsA in olive oil for 21 days. Within 1 week after discontinuing CsA, animals developed clinical signs of GVHD including runting, hunched posture, and severe diarrhea. This disease was fatal for greater than 80% of treated animals within 4 weeks after cessation of CsA. Furthermore, the induction of syngeneic GVHD did not appear to be linked to a particular MHC haplotype. Histologically, there was pronounced lymphoid atrophy of the spleen and thymus. Sections of large intestine showed an acute inflammatory process involving the mucosal layer ranging from single-cell destruction to complete mucosal ulceration. This murine model of GVHD should provide new opportunities for studying the development and regulation of autoimmune processes.

摘要

同基因移植物抗宿主病已被证明会在同基因大鼠辐射嵌合体经短疗程环孢素A(CsA)治疗后发生。然而,在小鼠系统中,关于该模型的数据一直存在争议。我们已成功地在用CsA短暂治疗的同基因小鼠辐射嵌合体中诱导出类似移植物抗宿主病(GVHD)的综合征。用950拉德剂量进行致死性照射的DBA/2小鼠用同基因骨髓进行重建,并每天腹腔注射15毫克/千克溶解于橄榄油中的CsA,持续21天。在停用CsA后1周内,动物出现了GVHD的临床症状,包括发育迟缓、弓背姿势和严重腹泻。这种疾病在停用CsA后4周内导致超过80%的受试动物死亡。此外,同基因GVHD的诱导似乎与特定的主要组织相容性复合体(MHC)单倍型无关。组织学上,脾脏和胸腺出现明显的淋巴样萎缩。大肠切片显示急性炎症过程,累及黏膜层,范围从单细胞破坏到完全黏膜溃疡。这种GVHD小鼠模型应为研究自身免疫过程的发展和调控提供新的机会。

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