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

被引:10
作者
Aibara, Nozomi [1 ]
Ohyama, Kaname [1 ]
Hidaka, Masaaki [2 ]
Kishikawa, Naoya [1 ]
Miyata, Yasuyoshi [3 ]
Takatsuki, Mitsuhisa [2 ]
Eguchi, Susumu [2 ]
Kurod, Naotaka [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, 1-7-1 Sakamoto Machi, Nagasaki 8528588, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Surg, Nagasaki, Japan
[3] Nagasaki Univ, Grad Sch Biomed Sci, Dept Urol, Nagasaki, Japan
关键词
Acute cellular rejection; Antigen; Circulating immune complexes; Immune complexome analysis; Liver transplantation; GROWTH-FACTOR-BETA; RHEUMATOID-ARTHRITIS; T-CELLS; THROMBOSPONDIN-1; CANCER; COMPLEMENT; EXPRESSION; PHENOTYPES; BIOMARKER; SYSTEM;
D O I
10.1016/j.trim.2018.02.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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.
引用
收藏
页码:60 / 64
页数:5
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