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与人间充质基质细胞治疗相关的同种异体免疫反应:一项系统综述

Alloreactive Immune Response Associated to Human Mesenchymal Stromal Cells Treatment: A Systematic Review.

作者信息

Sanabria-de la Torre Raquel, Quiñones-Vico María I, Fernández-González Ana, Sánchez-Díaz Manuel, Montero-Vílchez Trinidad, Sierra-Sánchez Álvaro, Arias-Santiago Salvador

机构信息

Cell Production and Tissue Engineering Unit, Virgen de las Nieves University Hospital, Andalusian Network of Design and Translation of Advanced Therapies, 18014 Granada, Spain.

Biosanitary Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.

出版信息

J Clin Med. 2021 Jul 5;10(13):2991. doi: 10.3390/jcm10132991.

Abstract

The well-known immunomodulatory and regenerative properties of mesenchymal stromal cells (MSCs) are the reason why they are being used for the treatment of many diseases. Because they are considered hypoimmunogenic, MSCs treatments are performed without considering histocompatibility barriers and without anticipating possible immune rejections. However, recent preclinical studies describe the generation of alloantibodies and the immune rejection of MSCs. This has led to an increasing number of clinical trials evaluating the immunological profile of patients after treatment with MSCs. The objective of this systematic review was to evaluate the generation of donor specific antibodies (DSA) after allogeneic MSC (allo-MSC) therapy and the impact on safety or tolerability. Data from 555 patients were included in the systematic review, 356 were treated with allo-MSC and the rest were treated with placebo or control drugs. A mean of 11.51% of allo-MSC-treated patients developed DSA. Specifically, 14.95% of these patients developed DSA and 6.33% of them developed cPRA. Neither the production of DSA after treatment nor the presence of DSA at baseline (presensitization) were correlated with safety and/or tolerability of the treatment. The number of doses administrated and human leucocyte antigen (HLA) mismatches between donor and recipient did not affect the production of DSA. The safety of allo-MSC therapy has been proved in all the studies and the generation of alloantibodies might not have clinical relevance. However, there are very few studies in the area. More studies with adequate designs are needed to confirm these results.

摘要

间充质基质细胞(MSCs)具有众所周知的免疫调节和再生特性,这就是它们被用于治疗多种疾病的原因。由于它们被认为免疫原性较低,因此在进行MSCs治疗时无需考虑组织相容性障碍,也无需预期可能的免疫排斥反应。然而,最近的临床前研究描述了同种异体抗体的产生以及MSCs的免疫排斥反应。这导致越来越多的临床试验评估患者接受MSCs治疗后的免疫状况。本系统评价的目的是评估异基因MSCs(allo-MSC)治疗后供体特异性抗体(DSA)的产生及其对安全性或耐受性的影响。系统评价纳入了555例患者的数据,其中356例接受了allo-MSC治疗,其余患者接受了安慰剂或对照药物治疗。接受allo-MSC治疗的患者平均有11.51%产生了DSA。具体而言,这些患者中有14.95%产生了DSA,其中6.33%产生了cPRA。治疗后DSA的产生以及基线时(致敏前)DSA的存在均与治疗的安全性和/或耐受性无关。给药剂量以及供体与受体之间的人类白细胞抗原(HLA)错配均不影响DSA的产生。所有研究均证实了allo-MSC治疗的安全性,同种异体抗体的产生可能不具有临床相关性。然而,该领域的研究非常少。需要更多设计合理的研究来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3216/8269175/f370e9a069f2/jcm-10-02991-g001.jpg

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