Transplantation Direct (Feb 2018)

Rituximab Induction to Prevent the Recurrence of PSC After Liver Transplantation—The Lessons Learned From ABO-Incompatible Living Donor Liver Transplantation

  • Yohei Yamada, MD, PhD,
  • Ken Hoshino, MD, PhD,
  • Yasushi Fuchimoto, MD, PhD,
  • Kentaro Matsubara, MD, PhD,
  • Taizo Hibi, MD, PhD,
  • Hiroshi Yagi, MD, PhD,
  • Yuta Abe, MD, PhD,
  • Masahiro Shinoda, MD, PhD,
  • Minoru Kitago, MD, PhD,
  • Hideaki Obara, MD, PhD,
  • Takahito Yagi, MD, PhD,
  • Hideaki Okajima, MD, PhD,
  • Toshimi Kaido, MD, PhD,
  • Shinji Uemoto, MD, PhD,
  • Tatsuya Suzuki, MD, PhD,
  • Keiichi Kubota, MD, PhD,
  • Tomoharu Yoshizumi, MD,
  • Yoshihiko Maehara, MD,
  • Yukihiro Inomata, MD, PhD,
  • Yuko Kitagawa, MD, PhD,
  • Hiroto Egawa, MD, PhD,
  • Tatsuo Kuroda, MD, PhD

DOI
https://doi.org/10.1097/TXD.0000000000000760
Journal volume & issue
Vol. 4, no. 2
p. e342

Abstract

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Background. Multiple studies have failed to reveal an effective method for preventing the recurrence of primary sclerosing cholangitis (PSC) after liver transplantation (LTx). A national study conducted in Japan revealed several risk factors for the recurrence after living donor LTx (LDLTx); however, recipients of ABO-blood type incompatible (ABO-I) LTx were excluded from the previous analysis. In the present study, we investigated the efficacy of an immunosuppressive protocol in ABO-I LTx on the recurrence of PSC after LDLTx. Methods. We conducted a national survey and analyzed the outcome of recipients who underwent ABO-I LDLTx for PSC (n = 12) between 1994 and 2010 in 9 centers and compared the outcome with that of ABO-compatible LDLTx for PSC (n = 96). The key elements of the immunosuppressive regimen in ABO-I LTx are plasma exchange sessions to remove existing antibodies, and the use of immunosuppression to control humoral immunity. Rituximab was added to the immunosuppression regimen from 2006 onward; 5 patients received rituximab perioperatively. Results. All 7 recipients who underwent ABO-I LDLTx before 2006 (who did not receive rituximab) died of infection (n = 3), antibody-mediated rejection (n = 1), ABO-incompatibility associated cholangiopathy (n = 1) or recurrence of PSC (n = 2). In contrast, we found that all 5 recipients from 2006 (who were treated with rituximab) retained an excellent graft function for more than 7 years without any recurrence of PSC. Conclusions. The findings of this study shed light on the efficacy of a novel strategy to prevent the recurrence of PSC and the possible mechanisms provided by rituximab treatment are discussed.