Zepeda-Quiroz Iván, Guzmán-Martín Carlos A, Peña-Peña Mario, Juárez-Villa José D, Soto-Abraham Maria V, Vázquez-Toledo Miguel A, Jiménez-Ortega Rogelio F, Moguel-González Bernardo, Osorio-Alonso Horacio, Sánchez-Muñoz Fausto, Flores-Gama César
Departamento de Nefrología, Instituto Nacional de Cardiología Ignacio Chávez, México City 14080, Mexico.
Departamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, México City 14080, Mexico.
J Clin Med. 2024 Mar 11;13(6):1600. doi: 10.3390/jcm13061600.
: Rejection continues to be the main cause of renal graft loss. Currently, the gold standard for diagnosis is an allograft biopsy; however, because it is time-consuming, costly, and invasive, the pursuit of novel biomarkers has gained interest. Variation in the expressions of miRNAs is currently considered a probable biomarker for the diagnosis of acute rejection. This study aimed to determine whether miR-150-5p in serum is related to microvascular damage in patients with acute antibody-mediated rejection (ABMR). : A total of 27 patients who underwent renal transplantation (RT) with and without ABMR were included in the study. We performed the quantification of hsa-miR-150-5p, hsa-miR-155, hsa-miR-21, hsa-miR-126, and hsa-miR-1 in plasma by RT-qPCR. The expressions between the groups and their correlations with the histological characteristics of the patients with ABMR were also investigated. : miR-150-5p significantly increased in the plasma of patients with rejection ( < 0.05), and the changes in miR-150-5p were directly correlated with microvascular inflammation in the allograft biopsies. Clinical utility was determined by ROC analysis with an area under the curve of 0.873. : Our results show that the patients with RT with ABMR exhibited increased expression of miR-150-5p compared to patients without rejection, which could have clinical consequences, as well as probable utility in the diagnosis of ABMR, and bioinformatics may help in unraveling the molecular mechanisms underlying ABMR conditions.
排斥反应仍然是肾移植失败的主要原因。目前,诊断的金标准是同种异体移植活检;然而,由于其耗时、成本高且具有侵入性,对新型生物标志物的探索引起了人们的兴趣。miRNA表达的变化目前被认为是诊断急性排斥反应的一种可能的生物标志物。本研究旨在确定血清中的miR-150-5p是否与急性抗体介导的排斥反应(ABMR)患者的微血管损伤有关。
本研究共纳入27例接受肾移植(RT)且有或无ABMR的患者。我们通过RT-qPCR对血浆中的hsa-miR-150-5p、hsa-miR-155、hsa-miR-21、hsa-miR-126和hsa-miR-1进行了定量分析。还研究了各组之间的表达情况及其与ABMR患者组织学特征的相关性。
排斥反应患者血浆中的miR-150-5p显著升高(<0.05),且miR-150-5p的变化与同种异体移植活检中的微血管炎症直接相关。通过ROC分析确定临床效用,曲线下面积为0.873。
我们的结果表明,与无排斥反应的患者相比,发生ABMR的RT患者miR-150-5p表达增加,这可能会产生临床后果,并且在ABMR的诊断中可能具有实用价值,生物信息学可能有助于揭示ABMR状况背后的分子机制。