血中氨基酸犬尿氨酸和吲哚氧苷酶水平预测急性移植物抗宿主病(aGVHD)

D. Ferreira, I. Silva, EG Lo Turco, Jsr Oliveira
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引用次数: 0

摘要

造血干细胞移植(HSCT)成功的主要障碍是急性移植物抗宿主病(aGVHD)。aGVHD的风险因素主要是临床因素,如果加入其他生物学因素,如代谢组学特征,可以改善。众所周知,测量的各种代谢产物的水平在免疫调节过程中很重要[1]。在我们的人群研究中,我们调查了26名(I组)同种异体移植受者的系统代谢状况。代谢组学研究采用靶向质谱法进行。26例患者在HSCT预处理方案前采集血浆。所有患者都进行了临床评估,直到移植后2年,然后I组被细分为IA亚组:16名出现aGVHD的患者和IB亚组:10名没有aGVHD患者。当比较IA亚组和IB亚组的代谢产物剂量时,观察到25种代谢产物。然后,我们通过生物信息学分析验证了Kynurenine/Tryptophan的比值,该比值估计了吲哚氧化酶(IDO)的活性。犬尿氨酸和IDO酶是代谢产物,在有关免疫耐受过程的文献中提供了临床证据。1998年,Mellor和Munn在动物模型中验证了IDO酶在孕妇异基因胎儿维持中的作用。因此,移植前对同种异体移植受者代谢组学特征的分析似乎有助于更好地了解免疫过程,并且较低剂量的犬尿氨酸和IDO活性酶在移植前可以识别出患aGVHD风险较高的患者。保留
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Blood Levels of the Amino Acid Kynurenine and Indoloxigenase are Predictive of Acute Graft Versus Host Disease (aGVHD)
The main barrier to the success of hematopoietic stem cell transplantation (HSCT) is acute graft versus host disease (aGVHD). The risk factors for aGVHD are mainly clinical and can be improved if additional biological factors are incorporated, such as the metabolomic profile. It is known that the levels of various metabolites measured are important in the process of immunoregulation [1]. In our population study we investigated the systemic metabolic profile for 26 (Group I) allotransplant recipients. The metabolomics study was carried out by Targeted Mass Spectrometry. Plasma samples of the 26 patients were collected before the Conditioning Regimen of HSCT. All patients were clinically evaluated until 2 years after transplant and then Group I was subdivided into subgroup IA: 16 patients that presented aGVHD and subgroup IB: 10 patients without aGVHD. When comparing the metabolites dosages from subgroup IA with those of subgroup IB, it was observed that 25 metabolites We then verified by bioinformatics analyses that the ratio Kynurenine/Tryptophan which estimates the Indoloxigenase (IDO) enzyme activity. Kynurenine and the IDO enzyme are metabolites that present clinical evidence in the literature regarding the immunotolerance process. The role of IDO enzyme in the maintenance of the allogeneic fetus in pregnant women was verified in an animal model in 1998 by Mellor and Munn. Thus, the pre-transplant analysis of the metabolomics profile of allotransplant recipients seems to contribute to a better understanding of immunological process and lower dosages of Kynurenine and IDO activity enzyme pre-transplant can identify patients at higher risk for developing aGVHD. RESEaRCh aRTICLE
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