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Evaluation of 131I-anti-MIF mAb as a reporter for allograft rejection.

机译:评估131I-抗MIF mAb作为同种异体移植排斥的报告基因。

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摘要

Finding a specific agent will be useful for monitoring allorejection in clinic. The macrophage migration inhibitory factor (MIF) was reported to be one of the major cytokines involved in allorejection. In this study, we evaluated whether (131)I-anti-MIF mAb could be an efficient imaging reporter for monitoring allorejection. (131)I-anti-MIF mAb or control (131)I-IgG was injected to skin allotransplantation mice and T/NT ratios were evaluated. The imaging changes of grafts were dynamically displayed by whole-body images. The results showed that up-regulation of MIF expression was found in allografts but not in isografts. During the whole progression of rejection, the T/NT ratio in the (131)I-anti-MIF mAb group was significantly higher than that in the (131)I-IgG group and markedly increased on the top of rejection. The graft-rejection could also be shown more clearly in the (131)I-anti-MIF mAb group by whole-body imaging. These results implied that (131)I-anti-MIF mAb may be a valid method for facilitating the development of protocols to monitor allorejection.
机译:寻找一种特定的药物将有助于监测临床中的异体注射。据报道,巨噬细胞迁移抑制因子(MIF)是参与Allorejecting的主要细胞因子之一。在这项研究中,我们评估了(131)I-抗MIF mAb是否可以作为监测异体注射的有效成像报告基因。将(131)I-抗MIF mAb或对照(131)I-IgG注入皮肤同种异体移植小鼠,并评估T / NT比。通过全身图像动态显示移植物的成像变化。结果表明,在同种异体移植物中发现了MIF表达的上调,而在同种异体移植物中则没有。在排斥的整个过程中,(131)I-抗MIF mAb组的T / NT比明显高于(131)I-IgG组,并且在排斥最高时显着增加。通过全身成像,在(131)I-抗MIF mAb组中也可以更清楚地显示出排斥反应。这些结果表明,(131)I-抗MIF mAb可能是促进开发监测同种异体注射协议的有效方法。

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