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Updated: Aug 5, 2026

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
Preformed HLA-DQ Donor-Specific Antibodies: Distinct Immunological Characteristics and Clinical Implications in
Hanbi Lee1,2, Jeeyoung Yoon1,2, Bioh Kim1,2
1Division of Nephrology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Abstract:
The aim of this study is to characterise the immunological features of preformed HLA-DQ DSAs and investigate their impact on post-transplant outcomes. Among 1540 ABO-compatible KT recipients with available high-resolution HLA typing at Seoul St. Mary's Hospital (January 2010-December 2024), 179 had preformed DSAs. Patients were classified into DQ group (n = 58), comprising those with DQ DSAs alone or in combination with other DSAs, and non-DQ (n = 121) group. We compared baseline DSA characteristics, desensitisation (DSZ) responses and post-transplant outcomes. The DQ group had a significantly higher proportion of re-transplant recipients. At baseline, DQ DSAs exhibited markedly higher MFI values compared to non-DQ DSAs. Following DSZ, 45.2% of DQ DSAs remained strong (MFI > 10,000), compared to only 2.8% of non-DQ DSAs. While the overall incidence of acute ABMR did not differ significantly between groups, a significant difference was observed in the temporal distribution and the characteristics of the associated DSAs. In early-onset ABMR, cases in the DQ group developed after the complete resolution of preformed DSAs, whereas those in the non-DQ group were associated with preformed DSAs. Late-onset ABMR occurred more frequently in the DQ group (41.7% vs. 10.0%, p = 0.024), and it developed with preformed DQ DSAs. Furthermore, allograft function showed a more rapid deterioration in the DQ group. Preformed DQ DSAs carry a higher immunological risk and exhibit greater resistance to treatment than non-DQ DSAs, and tend to cause late-onset acute ABMR rather than immediate post-transplant rejection. Therefore, more stringent immunological monitoring and immunosuppressive therapy are required.
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