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Donor-specific antibodies, glomerulitis, and human leukocyte antigen B eplet mismatch are risk factors for peritubular capillary C4d deposition in renal allografts
被引:0
|作者:
Zheng, Jin
[1
]
Guo, Hui
[2
]
Gong, Hui-Lin
[3
]
Lan, Ping
[4
]
Ding, Chen-Guang
[1
]
Li, Yang
[1
]
Ding, Xiao-Ming
[1
]
Xue, Wu-Jun
[1
]
机构:
[1] Xi An Jiao Tong Univ, Dept Kidney Transplantat, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
[2] Huazhong Univ Sci & Technol, Inst Organ Transplantat, Tongji Med Coll, Tongji Hosp, Wuhan 430030, Hubei, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Pathol, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Dept Nephrol, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
关键词:
Kidney transplantation;
C4d deposition;
donor-specific antibody;
Glomerulitis;
human leukocyte antigen eplet;
REJECTION;
PROSPECTS;
D O I:
10.1097/CM9.0000000000001685
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: The complement system plays an important role in the immune response to transplantation, and the diagnostic significance of peritubular capillary (PTC) C4d deposition (C4d+) in grafts is controversial. The study aimed to fully investigate the risk factors for PTC C4d+ and analyze its significance in biopsy pathology of kidney transplantation. Methods: This retrospective study included 124 cases of kidney transplant with graft biopsy and donor-specific antibody (DSA) testing from January 2017 to December 2019 in a single center. The effects of recipient pathological indicators, eplet mismatch (MM), and DSAs on PTC C4d+ were examined using univariate and multivariate logistic regression analyses. Results: In total, 35/124 (28%) were PTC C4d+, including 21 with antibody-mediated rejection (AMR), eight with renal tubular injury, three with T cell-mediated rejection, one with glomerular disease, and two others. Univariate analysis revealed that DSAs (P < 0.001), glomerulitis (P < 0.001), peritubular capillaritis (P < 0.001), and human leukocyte antigen (HLA) B eplet MM (P = 0.010) were the influencing factors of PTC C4d+. According to multivariate analysis, DSAs (odds ratio [OR]: 9.608, 95% confidence interval [CI]: 2.742-33.668, P < 0.001), glomerulitis (OR: 3.581, 95%CI: 1.246-10.289, P = 0.018), and HLA B eplet MM (OR: 1.166, 95%CI: 1.005-1.353, P = 0.042) were the independent risk factors for PTC C4d+. In receiver operating characteristic curve analysis, the area under the curve was increased to 0.831 for predicting PTC C4d+ when considering glomerulitis, DSAs, and HLA B eplet MM. The proportions of HLA I DSAs and PTC C4d+ in active antibody-mediated rejection were 12/17 and 15/17, respectively; the proportions of HLA class II DSAs and PTC C4d+ in chronic AMR were 8/12 and 7/12, respectively. Furthermore, the higher the PTC C4d+ score was, the more serious the urinary occult blood and proteinuria of recipients at the time of biopsy. Conclusions: PTC C4d+ was mainly observed in AMR cases. DSAs, glomerulitis, and HLA B eplet MM are the independent risk factors for PTC C4d+.
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页码:2874 / 2881
页数:8
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