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Updated: Jul 6, 2026

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
Preformed antibodies detected by cytotoxic assay or multibead array decrease liver allograft survival: role of human
Marcela Castillo-Rama1, Maria Jose Castro, Ivan Bernardo
1Department of Immunology, Hospital Doce de Octubre, Madrid, Spain. mcastillo.hdoc@salud.madrid.org
Donor-recipient human leukocyte antigen (HLA) compatibility has minimal impact on liver transplant survival. However, preformed HLA antibodies detected by Luminex and CDC crossmatch are linked to reduced graft survival and rejection.
Area of Science:
- Immunology
- Transplantation Medicine
- Genetics
Background:
- Human leukocyte antigen (HLA) compatibility and preformed antibodies are critical factors in organ transplantation, but their precise impact on liver graft survival requires further elucidation.
- Assessing donor-recipient HLA matching and the presence of preformed antibodies is essential for predicting transplant outcomes.
Purpose of the Study:
- To evaluate the influence of donor-recipient HLA compatibility and preformed antibodies on graft survival in a large cohort of liver transplant recipients.
- To compare the efficacy of complement-dependent cytotoxicity (CDC) and Luminex xMAP assays in detecting preformed antibodies and their association with transplant outcomes.
Main Methods:
- A single-center cohort study involving 896 liver transplants was analyzed.
- Kaplan-Meier survival analysis was used to assess the impact of HLA compatibility and preformed antibodies on allograft survival.
- Concordance between CDC and Luminex xMAP assays for antibody detection was evaluated.
Main Results:
- Donor-recipient HLA compatibility showed a marginal impact on overall allograft survival.
- Two mismatches at the HLA-A locus were associated with improved survival in retransplanted grafts.
- Preformed antibodies detected by both CDC and Luminex were significantly associated with shorter graft survival within the first year post-transplant.
- Positive CDC T crossmatches and Luminex-detected HLA class II antibodies were linked to decreased graft survival at both 1 and 5 years.
- The presence of preformed Luminex-detected antibodies correlated with an increased risk of allograft rejection.
Conclusions:
- While HLA typing may not be a prerequisite for liver transplantation, screening for HLA antibodies using Luminex techniques and performing CDC crossmatches can identify high-risk patients.
- Early detection of at-risk patients allows for intensified surveillance and personalized therapeutic strategies to improve graft survival.
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