Recipients Issues (Videos Available)

Wednesday July 04, 2018 from 08:30 to 09:30

Room: N-105

502.5 The clinical significance of pretransplant C1q assay status in positive crossmatch kidney transplantation

Soo Jin Kim, Korea

Yonsei University

Abstract

The Clinical Significance of Pretransplant C1q Assay Status in Positive Crossmatch Kidney Transplantation

Juhan Lee1, Deok Gie Kim1, Borae G Park2, Soo Jin Kim1, Sung Hoon Kim3, Yoon Bin Jung1, Jee Youn Lee1, Jae Geun Lee1, Man Ki Ju1, Beom Seok Kim4, Myoung Soo Kim1, Soon Il Kim1, Kyu Ha Huh1, Yu Seun Kim1.

1Transplantation Surgery, Yonsei University College of Medicine, Seoul, Korea; 2Laboratory Medicine, Asan Medical Center, Seoul, Korea; 3Surgery, Yonsei University Wonju College of Medicine, Wonju, Korea; 4Nephrology, Yonsei University College of Medicine, Seoul, Korea

Background: Patients with a pretransplant donor-specific antibodies (DSA) are at higher risk for antibody-mediated rejection (AMR). However, not all DSA have the same pathogenetic potential. The novel assay for complement binding capacity may help to stratify the risk for AMR. The aim of this study was to investigate the association between complement binding ability of DSA and clinical outcomes in patients with a positive crossmatch (XM).
Methods: We analyzed 59 patients with a positive XM who underwent living donor kidney transplantation between 2011 and 2016 with desensitization therapy (12 complement-dependent cytotoxic [CDC] XM and 47 flow cytometric XM). We analyzed clinical outcomes according to XM and C1q status.
Results: Biopsy-proven AMR developed in 18 patients (30.5%). CDC XM patients suffered more AMR than flow cytometric XM patients (P=0.004). Although the incidence of AMR was higher in C1q-positive DSA than in C1q-negative DSA, the difference was not statistically significant (P=0.067).  The XM techniques and C1q positivity did no correlated with graft loss. C1q positivity was associated with higher IgG titer (11181 ± 3997 vs. 4823 ± 6132, P=0.002).
Conclusion: C1q-positive DSA in patients with positive crossmatch was unable to predict AMR, but CDC XM compared to flow cytometric XM did. The C1q binding activity in patients with positive XM largely reflects differences in antibody strength.



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