Outcome of ABO Blood Type-Incompatible Living-Related Donor Kidney Transplantation Under a Contemporary Immunosuppression Strategy in Japan.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Historique:
received: 28 12 2019
accepted: 22 01 2020
pubmed: 26 5 2020
medline: 15 12 2020
entrez: 26 5 2020
Statut: ppublish

Résumé

Because of the serious donor shortage in Japan, there is an increasing need for ABO blood type-incompatible kidney transplantation (ABOi-KT) in living-related donor kidney transplantation. We evaluated the outcomes of ABOi-KT performed at our hospitals using a contemporary immunosuppression strategy with low-dose rituximab. Between June 2006 and April 2019, 107 patients underwent living-related donor kidney transplantation at our hospitals. The patients were divided into ABO-compatible (ABOc) and ABOi groups. The basic immunosuppression regimen differed between the 2 groups in the use of low-dose rituximab and therapeutic apheresis in the ABOi group. We compared graft survival, patient survival, rejection, viral infection, and posttransplant renal function between the 2 groups. Of 107 recipients, 37 (35%) underwent ABOi-KT. The 5-year graft survival rates in the ABOc and ABOi group were 91% and 100%, respectively. The Kaplan-Meier analyses showed no difference in graft survival (P = .168) or patient survival (P = .873) between the groups. Biopsy-proven rejection in the ABOc and ABOi groups was observed in 13 (19%) and 7 (19%) patients, respectively (P = .965), and viral infection was observed in 21 (30%) and 10 (27%) patients (P = .747), respectively. Renal function by estimated glomerular filtration rate from 1 week to 5 years after transplantation was similar in both groups. The outcomes of ABOi-KT with low-dose rituximab were comparable with those of ABOc-KT at our hospitals. ABOi-KT with proper immunosuppression may be an option to help resolve the severe donor shortage in Japan.

Sections du résumé

BACKGROUND BACKGROUND
Because of the serious donor shortage in Japan, there is an increasing need for ABO blood type-incompatible kidney transplantation (ABOi-KT) in living-related donor kidney transplantation. We evaluated the outcomes of ABOi-KT performed at our hospitals using a contemporary immunosuppression strategy with low-dose rituximab.
PATIENTS AND METHODS METHODS
Between June 2006 and April 2019, 107 patients underwent living-related donor kidney transplantation at our hospitals. The patients were divided into ABO-compatible (ABOc) and ABOi groups. The basic immunosuppression regimen differed between the 2 groups in the use of low-dose rituximab and therapeutic apheresis in the ABOi group. We compared graft survival, patient survival, rejection, viral infection, and posttransplant renal function between the 2 groups.
RESULTS RESULTS
Of 107 recipients, 37 (35%) underwent ABOi-KT. The 5-year graft survival rates in the ABOc and ABOi group were 91% and 100%, respectively. The Kaplan-Meier analyses showed no difference in graft survival (P = .168) or patient survival (P = .873) between the groups. Biopsy-proven rejection in the ABOc and ABOi groups was observed in 13 (19%) and 7 (19%) patients, respectively (P = .965), and viral infection was observed in 21 (30%) and 10 (27%) patients (P = .747), respectively. Renal function by estimated glomerular filtration rate from 1 week to 5 years after transplantation was similar in both groups.
CONCLUSIONS CONCLUSIONS
The outcomes of ABOi-KT with low-dose rituximab were comparable with those of ABOc-KT at our hospitals. ABOi-KT with proper immunosuppression may be an option to help resolve the severe donor shortage in Japan.

Identifiants

pubmed: 32448659
pii: S0041-1345(19)31771-3
doi: 10.1016/j.transproceed.2020.01.152
pii:
doi:

Substances chimiques

ABO Blood-Group System 0
Immunologic Factors 0
Rituximab 4F4X42SYQ6

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1700-1704

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Itsuto Hamano (I)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Shingo Hatakeyama (S)

Department of Advanced Blood Purification Therapy, Hirosaki, Japan. Electronic address: shingoh@hirosaki-u.ac.jp.

Takeshi Fujita (T)

Department of Cardiology and Nephrology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Reiichi Murakami (R)

Department of Cardiology and Nephrology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Tomoko Hamaya (T)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Kyo Togashi (K)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Yuichiro Suzuki (Y)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Hayato Yamamoto (H)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Tohru Yoneyama (T)

Department of Advanced Transplant and Regenerative Medicine, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Takahiro Yoneyama (T)

Department of Advanced Transplant and Regenerative Medicine, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Yasuhiro Hashimoto (Y)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Shunji Narumi (S)

Department of Transplant Surgery, Nagoya Daini Red Cross Hospital, Nagoya, Japan.

Hirofumi Tomita (H)

Department of Cardiology and Nephrology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Chikara Ohyama (C)

Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Cardiology and Nephrology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

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