論文

査読有り
2009年2月

Requirement of Protocol Biopsy Before and After Complete Cessation of Immunosuppression After Liver Transplantation

TRANSPLANTATION
  • Mami Yoshitomi
  • Takaaki Koshiba
  • Hironori Haga
  • Ying Li
  • Xiangdong Zhao
  • Donghua Cheng
  • Aya Miyagawa
  • Hiromi Sakashita
  • Tatsuaki Tsuruyama
  • Hidenori Ohe
  • Mikiko Ueda
  • Shinya Okamoto
  • Hiroto Egawa
  • Kathryn Wood
  • Shimon Sakaguchi
  • Toshiaki Manabe
  • Koichi Tanaka
  • Shinji Uemoto
  • 全て表示

87
4
開始ページ
606
終了ページ
614
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1097/TP.0b013e318195a7cb
出版者・発行元
LIPPINCOTT WILLIAMS & WILKINS

Background. Operational tolerance is defined as long-term acceptance of a transplanted organ after complete cessation of immunosuppression (IS), but may not always protect against antigen-dependent changes in graft morphology.
Method. IS free patients after living-donor liver transplantation (LDLT) underwent protocol biopsy (tolerance group [Gr-Tol]) and were evaluated for rejection and fibrosis. The degree of fibrosis was compared with those in the patients on maintenance IS group (Gr-IS) and the base line normal liver group (Gr-BS). When bridging fibrosis or progression of fibrosis was observed, IS was reintroduced or increased in Gr-Tol or in the patients in the weaning process.
Results. Neither acute nor chronic rejection was observed. The degree of fibrosis, however, was significantly greater in Gr-Tol than those in Gr-IS and Gr-BS. In Gr-Tol, the number of graft infiltrating FOXP3(+) cells was significantly increased, the interval between LDLT and biopsy plus the donor age was significantly longer, and recipient age at LDLT was significantly younger, compared with those in Gr-IS. However, none of these three parameters correlated with the degree of fibrosis. In 7 of 11 patients in whom IS was reintroduced or increased, the improvement of fibrosis was observed by the subsequent biopsy.
Conclusion. Grafts of operationally tolerant patients after LDLT did not exhibit acute or chronic rejection, but they exhibited fibrosis. It remains elusive whether fibrosis observed in tolerant grafts is antigen dependent. The finding that the reintroduction or the increase of IS fibrosis was improved supported the possibility that fibrosis in operationally tolerant after patients was antigen dependent.

リンク情報
DOI
https://doi.org/10.1097/TP.0b013e318195a7cb
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/19307800
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000263643400021&DestApp=WOS_CPL
ID情報
  • DOI : 10.1097/TP.0b013e318195a7cb
  • ISSN : 0041-1337
  • PubMed ID : 19307800
  • Web of Science ID : WOS:000263643400021

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