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Noninvasive graft monitoring using donor-derived cell-free DNA in Japanese liver transplantation.
Kanamori, Hiroki; Yamada, Yohei; Ito, Yoko; Shirosaki, Koji; Yamagishi, Satoko; Maeda, Yutaro; Kudo, Yumi; Umeyama, Tomoshige; Takahashi, Nobuhiro; Kato, Mototoshi; Hasegawa, Yasushi; Matsubara, Kentaro; Shinoda, Masahiro; Obara, Hideaki; Irie, Rie; Tsujikawa, Hanako; Okita, Hajime; Nguyen, Phuong Thanh; Saigo, Kenichi; Mitsunaga, Shigeki; Inoue, Ituro; Kitagawa, Yuko; Kuroda, Tatsuo.
Afiliação
  • Kanamori H; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Yamada Y; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Ito Y; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Shirosaki K; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Yamagishi S; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Maeda Y; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Kudo Y; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Umeyama T; Department of Pediatric Surgery, St Luke's International Hospital, Tokyo, Japan.
  • Takahashi N; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Kato M; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Hasegawa Y; Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Matsubara K; Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Shinoda M; Digestive Diseases Center, International University of Health and Welfare School of Medicine, Mita Hospital, Tokyo, Japan.
  • Obara H; Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Irie R; Department of Diagnostic Pathology, Nippon Koukan Hospital, Kawasaki, Japan.
  • Tsujikawa H; Division of Diagnostic Pathology, Keio University School of Medicine, Tokyo, Japan.
  • Okita H; Division of Diagnostic Pathology, Keio University School of Medicine, Tokyo, Japan.
  • Nguyen PT; Human Genetics Laboratory, National Institute of Genetics, Mishima, Japan.
  • Saigo K; Department of Transplantation Surgery, Japan Community Health Care Organization, Chiba Hospital, Chiba, Japan.
  • Mitsunaga S; Human Genetics Laboratory, National Institute of Genetics, Mishima, Japan.
  • Inoue I; Human Genetics Laboratory, National Institute of Genetics, Mishima, Japan.
  • Kitagawa Y; Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Kuroda T; Department of Pediatric Surgery, Keio University School of Medicine, Tokyo, Japan.
Hepatol Res ; 54(3): 300-314, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37850337
AIM: To evaluate the use of donor-derived cell-free DNA (dd-cfDNA) in diagnosing graft injuries in Japanese liver transplantation (LTx), including family-related living donors. METHODS: A total of 321 samples from 10 newly operated LTx recipients were collected to monitor the early dynamics of dd-cfDNA levels after LTx. Fifty-five samples from 55 recipients were collected during protocol biopsies (PB), whereas 36 samples from 27 recipients were collected during event biopsies, consisting of 11 biopsy-proven acute rejection (AR), 20 acute dysfunctions without rejection (ADWR), and 5 chronic rejections. The levels of dd-cfDNA were quantified using a next-generation sequencer based on single nucleotide polymorphisms. RESULTS: The dd-cfDNA levels were elevated significantly after LTx, followed by a rapid decline to the baseline in patients without graft injury within 30 days post-LTx. The dd-cfDNA levels were significantly higher in the 11 samples obtained during AR than those obtained during PB (p < 0.0001), which decreased promptly after treatment. The receiver operator characteristic curve analysis of diagnostic ability yielded areas under the curve of 0.975 and 0.897 for AR (rejection activity index [RAI] ≥3) versus PB and versus non-AR (ADWR + PB). The dd-cfDNA levels during AR were elevated earlier and correlated more strongly with the RAI (r = 0.740) than aspartate aminotransferase/alanine aminotransferase. The dd-cfDNA levels were neither associated with graft fibrosis based on histology nor the status of donor-specific antibodies in PB samples. CONCLUSIONS: Donor-derived cell-free DNA serves as a sensitive biomarker for detecting graft injuries in LTx. Further large-scale cohort studies are warranted to optimize its use in differentiating various post-LTx etiologies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hepatol Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hepatol Res Ano de publicação: 2024 Tipo de documento: Article