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既往输血-环孢素诱导耐受的机制:免疫细胞嵌合体的潜在作用。

Mechanisms of prior blood transfusion-cyclosporine-induced tolerance: a potential role for immune-cellular chimerism.

作者信息

Beko K R, Tran H O, Hewitt C W, Black K S, Patel M P, Ramsamooj R, Martin D C

机构信息

Department of Surgery, University of California, Irvine 92717.

出版信息

Transplant Proc. 1991 Feb;23(1 Pt 1):147-8.

PMID:1990500
Abstract

Skin allografts were not enhanced by prior conditioning of blood and CyA (5 or 10 mg/kg/d). However, when BM-CyA pretreatment was used, SA survival was significantly prolonged (CyA, 5 or 10 mg/kg/d). In examining differences between the BT-CyA and BM-CyA protocols, equivocal levels of donor microchimerism (1.5%) were found in the spleens of BT-CyA conditioned recipients at the time of transplantation (day 0). In contrast, highly significant levels of splenic donor chimerism (17.2%) developed at day 0 for the BM-CyA pretransplant recipients. Skin-allograft prolongation under the BM-CyA protocol implied that the effect may be linked to the existence of a donor-specific stem-cell population in the recipient animal.

摘要

血液预先处理及使用环孢素A(5或10毫克/千克/天)并未增强皮肤同种异体移植效果。然而,当采用骨髓-环孢素A预处理时,皮肤同种异体移植存活时间显著延长(环孢素A,5或10毫克/千克/天)。在研究骨髓移植-环孢素A方案与血液输注-环孢素A方案之间的差异时,在移植时(第0天)发现血液输注-环孢素A预处理受体的脾脏中存在模糊水平的供体微嵌合体(1.5%)。相比之下,骨髓移植-环孢素A预处理受体在第0天脾脏中出现了高度显著水平的供体嵌合体(17.2%)。骨髓移植-环孢素A方案下皮肤同种异体移植存活时间的延长表明,这种效应可能与受体动物中供体特异性干细胞群的存在有关。

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