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Maternal grafts protect daughter recipients from acute cellular rejection after pediatric living donor liver transplantation for biliary atresia. | LitMetric

AI Article Synopsis

  • Some studies indicate that gender mismatches between liver donors and recipients can negatively affect graft prognosis, yet there's limited research on its role in acute cellular rejection (ACR) in pediatric liver transplants.
  • This study analyzed 114 pediatric living donor liver transplants, focusing on the relationship between gender mismatch and ACR incidence in recipients with biliary atresia.
  • Results showed a 36.8% incidence of ACR, with gender mismatch identified as a significant independent risk factor, particularly noting that paternal grafts in gender mismatch situations led to more ACR cases than maternal grafts.

Article Abstract

Some studies have found that gender mismatch between donors and recipients are related to poor graft prognosis after liver transplantation. However, few studies have investigated the impact of gender mismatch on acute cellular rejection (ACR) in pediatric living donor liver transplantation (LDLT). This retrospective study investigated the clinical significance of these factors in ACR after pediatric LDLT. Between November 2001 and February 2012, 114 LDLTs were performed for recipients with biliary atresia (BA) using parental grafts. We performed univariate and multivariate analyses to identify the factors associated with ACR. The donor-recipient classifications included mother donor to daughter recipient (MD; n = 43), mother to son (n = 18), father to daughter (FD; n = 33), and father to son (n = 20) groups. The overall incidence rate of ACR in the recipients was 36.8%. Multivariate analysis showed that gender mismatch alone was an independent risk factor for ACR (P = 0.012). The FD group had a higher incidence of ACR than the MD group (P = 0.002). In LDLT, paternal grafts with gender mismatch were associated with a higher increased incidence of ACR than maternal grafts with gender match. Our findings support the possibility that maternal antigens may have an important clinical impact on graft tolerance in LDLT for patients with BA.

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Source
http://dx.doi.org/10.1111/tri.12273DOI Listing

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