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Findings of graft biopsy specimens within 90 days after ABO blood group incompatible living donor kidney transplantation compared with ABO‐identical and non‐identical transplantation
Author(s) -
Ushigome Hidetaka,
Okamoto Masahiko,
Koshino Katsuhiro,
Nobori Syuji,
Okajima Hideaki,
Masuzawa Naoko,
Urasaki Koji,
Yoshimura Norio
Publication year - 2010
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/j.1399-0012.2010.01278.x
Subject(s) - abo blood group system , medicine , transplantation , kidney transplantation , biopsy , kidney , gastroenterology , surgery , urology
Ushigome H, Okamoto M, Koshino K, Nobori S, Okajima H, Masuzawa N, Urasaki K, Yoshimura N. Findings of graft biopsy specimens within 90 days after ABO blood group incompatible living donor kidney transplantation compared with ABO‐identical and non‐identical transplantation.
Clin Transplant 2010: 24 (Suppl. 22): 16–21. © 2010 John Wiley & Sons A/S. Abstract:  As immunosuppressive therapy has advanced, we have markedly improved the outcome of ABO blood group incompatible living donor kidney transplantation. Consequently, graft survival at early phase after ABO‐incompatible transplantation has been favorable than ABO‐compatible transplantation in Japan. But in these days, it has been assumed that transplant glomerulopathy within one yr after ABO‐incompatible kidney transplantation might be significantly precipitated. That may be because of chronic, active antibody‐mediated rejection (AMR). We performed kidney graft biopsies at the early phase within 90 d after living donor kidney transplantation that involved the episode and protocol biopsies and studied findings of graft biopsy specimens when compared with ABO incompatible and compatible involving non‐identical and identical transplantations. In ABO‐incompatible transplant cases, the ratio occurring glomerulitis, especially severe injury of g 2–3, was significantly higher than that of identical and non‐identical transplant cases (p < 0.01). There was no significant difference in t score, i score, ptc score and v score between three transplant groups. The cases occurring AMR were concordant with the cases recognized with severe glomerulitis. AMR was difficult to be diagnosed by C4d analysis in ABO‐incompatible transplant cases. Glomerular injury score, g score, may be considered as more significant and the injury should be cured thoroughly.

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