| Literature DB >> 28792635 |
Manabu Okada1,2, Yoshihiko Watarai1, Kenta Iwasaki3, Kenta Murotani4, Kenta Futamura1, Takayuki Yamamoto1, Takahisa Hiramitsu1, Makoto Tsujita1, Norihiko Goto1, Shunji Narumi1, Asami Takeda5, Kunio Morozumi6, Kazuharu Uchida2,3, Takaaki Kobayashi2.
Abstract
The effectiveness of desensitization with rituximab in ABO-incompatible renal transplantation (ABO-I) has been widely reported. However, ABO-I outcomes are still worse than those of ABO-identical or ABO-compatible renal transplantation (ABO-Id/C). We retrospectively examined the outcomes in consecutive living donor ABO-Id/C (n = 412) and ABO-I (n = 205) cases to elucidate the causes of inferiority in ABO-I. ABO-I cases included recipients treated with rituximab (RIT, n = 131), splenectomy (SPX, n = 21), or neither because of low anti-A/B antibody titers (NoR/S, n = 53). Graft survival, infection, and de novo HLA antibody production were compared for ABO-I and ABO-Id/C, followed by stratification into RIT and NoR/S groups. Propensity score-based methods were employed to limit selection bias and potential confounders. Overall graft survival for ABO-I was significantly lower than that for ABO-Id/C (92.8% vs 97.2% after 5 years, P = .0037). Graft loss due to infection with ABO-I was significantly more frequent than that with ABO-Id/C, whereas acute antibody-mediated rejection (AMR) caused no graft failure in ABO-I recipients. Stratified analysis demonstrated significantly higher infection risk with RIT than with NoR/S. Safe reduction or avoidance of rituximab in desensitization protocols might contribute to further improvement of ABO-I outcome.Entities:
Keywords: ABO-incompatible kidney transplantation; rituximab
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Year: 2017 PMID: 28792635 DOI: 10.1111/ctr.13071
Source DB: PubMed Journal: Clin Transplant ISSN: 0902-0063 Impact factor: 2.863