Abstract

Few data on husband-to-wife transplantations with mutual children (H2W) exist in the current era. We investigated the outcome of H2W transplantations (n = 25) treated with T cell-depleting induction compared to women with prior pregnancies also receiving their first HLA-mismatched kidney transplant, but from a different donor source: (i) other living donor (n = 52) and (ii) deceased donor (n = 120). Seventy-four percent of the women had ≥2 pregnancies; median follow-up time was 5 years. Death-censored allograft survival was significantly lower in the H2W group compared to the other two groups (p = 0.03). Three of four graft losses in the H2W group were due to rejection. 5-year patient survival in the H2W group was high and similar compared to the other living donor group (100 vs. 98%; p = 0.28). The incidence of (sub)clinical antibody-mediated rejection was higher in the H2W group (36 vs. 20 vs. 18%) (p = 0.10). The frequency of infections was similar among the three groups. No immunological parameter was predictive for rejection or graft loss in H2W transplantations. In conclusion, H2W transplantation is a valuable option, but associated with a higher risk for allograft loss due to rejection despite T cell-depleting induction. Further research is required for better risk prediction on an individual patient level.

Highlights

  • IntroductionUsing sensitive single antigen bead assays on the Luminex platform, child-specific HLA-directed antibodies are detected immediately after delivery in about 20–30% of women after one pregnancy and almost 50% after three or more pregnancies [1]

  • Pregnancy is an important reason for HLA-directed sensitization

  • The key observation is this study was that despite T celldepleting induction, H2W transplantations have a higher risk for death-censored graft loss possibly mediated by a higher frequency of antibodymediated rejection (ABMR) compared to other HLAmismatched living or deceased donor transplantations in women with prior pregnancies

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Summary

Introduction

Using sensitive single antigen bead assays on the Luminex platform, child-specific HLA-directed antibodies are detected immediately after delivery in about 20–30% of women after one pregnancy and almost 50% after three or more pregnancies [1]. This suggests that repeated exposures to the same HLA molecules increases the likelihood of a detectable humoral immune response [2, 3]. As sera dating back to the immediate time after delivery are very rarely available, sensitization cannot be excluded, even if no HLA antibodies are detectable in current sera This is a major diagnostic challenge in husband-to-wife transplantations with mutual children (H2W), because there will be a 20–50% chance of prior husband-specific sensitization depending on the number of pregnancies. Several case reports/series demonstrated that severe early rejection can occur in H2W transplantations despite the absence of detectable HLA antibodies prior to transplantation [7,8,9,10]

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