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Immune complexome analysis of antigens in circulating immune complexes from patients with acute cellular rejection after living donor liver transplantation

机译:急性细胞排斥患者肝脏肝移植术后急性细胞排斥患者抗原免疫复合物分析

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摘要

Liver transplantation is a life-saving procedure for many end-stage liver diseases; however, rejection after transplantation is still occurs in some recipients. The most common form of rejection is T cell-related acute cellular rejection (ACR). To understand the mechanism of rejection, it is necessary to identify immune targets. Since the development of B cell immunity depends upon concordant T cell immunity, we hypothesized that rejection-specific antigens in circulating immune complexes (CICs) may be present in the sera of recipients experiencing rejection, and as such, may be useful as diagnostic biomarkers for ACR. The purpose of this study was to investigate rejection-specific antigens in CICs (CIC-antigens) in serum of ACR patients. We applied immune complexome analysis, in which CICs are separated from whole serum and then subjected to direct tryptic digestion and identification of CIC-antigens by nano-liquid chromatography-tandem mass spectrometry, to sera of 32 living donor liver transplant recipients (10 recipients experienced ACR and the others did not experience). CIC-antigens were compared between rejection and non-rejection groups to elucidate those that were only detected in the rejection group. We identified 11 CIC-antigens that were only detected in patients who experienced rejection, 4 of which (thrombospondin-1, apolipoprotein E, apolipoprotein C-III, and complement factor H) were only detected during ACR.
机译:肝移植是许多末期肝病的省力程序;然而,在移植后排斥仍然发生在某些接受者中。最常见的抑制形式是与T细胞相关的急性细胞排斥(ACR)。要了解拒绝机制,有必要识别免疫目标。由于B细胞免疫力的发展取决于一致的T细胞免疫,我们假设循环免疫复合物(CICS)中的抑制特异性抗原可能存在于经历排斥的受者的血清中,因此可用作诊断生物标志物ACR。本研究的目的是在ACR患者血清中调查CICS(CIC-抗原)中的抑制特异性抗原。我们应用免疫复杂分析,其中CICS与全血清分离,然后通过纳米液相色谱 - 串联质谱法直接胰蛋白酶消化和鉴定CIC抗原,达到32名活体供体肝移植受者的血清(10名受者ACR和其他人没有经历过)。在排斥和非排斥基团之间比较CIC-抗原,以阐明仅在排斥项中检测到的那些。我们鉴定了11名CIC-抗原,其仅在经历抑制的患者中检测到,其中4(血小板环戊蛋白-1,载脂蛋白E,载脂蛋白C-III和补体H)均仅在ACR期间检测到。

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