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基因工程间充质基质细胞作为治疗严重急性移植物抗宿主病的新趋势。

Genetically engineered mesenchymal stromal cells as a new trend for treatment of severe acute graft-versus-host disease.

机构信息

Cellular and Molecular Research Center, Research Institute for Prevention of Non-communicable Disease, Qazvin University of Medical Science, Qazvin, Iran.

Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Clin Exp Immunol. 2022 May 13;208(1):12-24. doi: 10.1093/cei/uxac016.

Abstract

Mesenchymal stem cells (MSCs) are a population of non-hematopoietic and self-renewing cells characterized by the potential to differentiate into different cell subtypes. MSCs have interesting features which have attracted a lot of attention in various clinical investigations. Some basic features of MSCs are including the weak immunogenicity (absence of MHC-II and costimulatory ligands accompanied by the low expression of MHC-I) and the potential of plasticity and multi-organ homing via expressing related surface molecules. MSCs by immunomodulatory effects could also ameliorate several immune-pathological conditions like graft-versus-host diseases (GVHD). The efficacy and potency of MSCs are the main objections of MSCs therapeutic applications. It suggested that improving the MSC immunosuppressive characteristic via genetic engineering to produce therapeutic molecules consider as one of the best options for this purpose. In this review, we explain the functions, immunologic properties, and clinical applications of MSCs to discuss the beneficial application of genetically modified MSCs in GVHD.

摘要

间充质干细胞(MSCs)是一群非造血且具有自我更新能力的细胞,其特征是具有分化为不同细胞亚型的潜能。MSCs 具有许多有趣的特性,这在各种临床研究中引起了广泛关注。MSCs 的一些基本特征包括弱免疫原性(缺乏 MHC-II 和共刺激配体,同时 MHC-I 表达水平较低)和通过表达相关表面分子实现可塑性和多器官归巢的潜能。MSCs 通过免疫调节作用还可以改善移植物抗宿主病(GVHD)等几种免疫病理状况。MSCs 的疗效和效力是 MSC 治疗应用的主要关注点。通过遗传工程提高 MSC 的免疫抑制特性,以产生治疗性分子,被认为是达到这一目的的最佳选择之一。在这篇综述中,我们解释了 MSCs 的功能、免疫特性和临床应用,以探讨基因修饰 MSCs 在 GVHD 中的有益应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c449/9113247/015dda21e49f/uxac016_fig4.jpg

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