肝移植后血清角蛋白浓度的时间变化:角蛋白18和角蛋白19片段的对比结果。

Case Reports in Hepatology Pub Date : 2020-11-30 eCollection Date: 2020-01-01 DOI:10.1155/2020/8895435
Cristina Macía, Jose Loureiro, Isabel Campos-Varela, Ihab Abdulkader, Esteban Otero, Evaristo Varo, Santiago Tomé, Arturo Gonzalez-Quintela
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引用次数: 1

摘要

目的:正常情况下,成人肝细胞仅表达角蛋白8 (K8)和角蛋白18 (K18),而胆管细胞也表达K19。在这项研究中,我们描述了肝移植后血清K19和K18水平的正常时间变化模式。患者和方法。在11例成年患者肝移植后的基线和定期间隔(长达6个月)测量血清中K19片段CYFRA 21-1、K18片段组织多肽特异性抗原(TPS)和M30(凋亡过程中caspase切割后产生的一种新表位)的水平。结果:移植后血清K19浓度从基线值逐渐下降,其时间过程模式与血清胆红素相似。相比之下,K18片段的血清浓度在移植后不久显著增加,随后逐渐下降,其时间过程模式与血清转氨酶相似。TPS的增加往往比M30出现得更早,这表明移植后第一天肝细胞以坏死为主,随后以凋亡为主。5例患者出现移植后并发症(3例急性排斥反应,2例HCV复发)。在所有病例中均观察到早期血清K19浓度升高。2例HCV复发患者血清K18片段(M30和TPS)浓度升高,3例急性排斥反应患者血清K18片段(M30和TPS)浓度变化更大。结论:肝移植后血清中K19和K18片段的浓度具有不同的时间变化模式。这些正常模式变化的诊断价值应在未来的研究中加以解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Time-Course Changes of Serum Keratin Concentrations after Liver Transplantation: Contrasting Results of Keratin-18 and Keratin-19 Fragments.

Time-Course Changes of Serum Keratin Concentrations after Liver Transplantation: Contrasting Results of Keratin-18 and Keratin-19 Fragments.

Time-Course Changes of Serum Keratin Concentrations after Liver Transplantation: Contrasting Results of Keratin-18 and Keratin-19 Fragments.

Time-Course Changes of Serum Keratin Concentrations after Liver Transplantation: Contrasting Results of Keratin-18 and Keratin-19 Fragments.

Objective: Under normal conditions, adult hepatocytes express only keratin-8 (K8) and keratin-18 (K18), whereas cholangiocytes also express K19. In this study, we delineate the pattern of normal time-course changes in serum K19 and K18 levels after liver transplantation. Patients and Methods. Serum levels of the K19 fragment CYFRA 21-1 and the K18 fragments tissue polypeptide specific antigen (TPS) and M30 (a neoepitope that is generated after caspase cleavage during apoptosis) were measured at baseline and at regular intervals (up to 6 months) after liver transplantation in 11 adult patients.

Results: There was a gradual decrease in serum K19 concentrations from baseline values after transplantation, following a time-course pattern similar to that of serum bilirubin. In contrast, serum concentrations of K18 fragments increased markedly shortly after transplantation and gradually decreased thereafter, following a time-course pattern similar to that of serum transaminases. The increase in TPS tended to occur earlier than that in M30, suggesting an initial predominance of hepatocyte necrosis followed by a predominance of apoptosis in the first days after transplantation. Five patients presented posttransplant complications (acute rejection in three cases and HCV recurrence in two cases). An early increase in serum K19 concentrations was observed in all cases. An increase in serum concentrations of K18 fragments (M30 and TPS) was observed in the two cases with HCV recurrence and was more variable in the three cases with acute rejection.

Conclusions: Serum concentrations of K19 and K18 fragments follow a dissimilar pattern of time-course changes after liver transplantation. The diagnostic value of variations in these normal patterns should be addressed in future studies.

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