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Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation

BACKGROUND: Tacrolimus (TAC) is a key immunosuppressant drug for kidney transplantation (KTx). However, the optimal serum trough level of TAC for good long-term outcomes remains unclear. This study aimed to investigate the relationship between the maintenance TAC trough level and the appearance of d...

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Autores principales: Unagami, Kohei, Ishida, Hideki, Furusawa, Miyuki, Kitajima, Kumiko, Hirai, Toshihito, Kakuta, Yoichi, Toki, Daisuke, Shimizu, Tomokazu, Omoto, Kazuya, Okumi, Masayoshi, Nitta, Kosaku, Tanabe, Kazunari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160958/
https://www.ncbi.nlm.nih.gov/pubmed/33280052
http://dx.doi.org/10.1093/ndt/gfaa258
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author Unagami, Kohei
Ishida, Hideki
Furusawa, Miyuki
Kitajima, Kumiko
Hirai, Toshihito
Kakuta, Yoichi
Toki, Daisuke
Shimizu, Tomokazu
Omoto, Kazuya
Okumi, Masayoshi
Nitta, Kosaku
Tanabe, Kazunari
author_facet Unagami, Kohei
Ishida, Hideki
Furusawa, Miyuki
Kitajima, Kumiko
Hirai, Toshihito
Kakuta, Yoichi
Toki, Daisuke
Shimizu, Tomokazu
Omoto, Kazuya
Okumi, Masayoshi
Nitta, Kosaku
Tanabe, Kazunari
author_sort Unagami, Kohei
collection PubMed
description BACKGROUND: Tacrolimus (TAC) is a key immunosuppressant drug for kidney transplantation (KTx). However, the optimal serum trough level of TAC for good long-term outcomes remains unclear. This study aimed to investigate the relationship between the maintenance TAC trough level and the appearance of de novo donor-specific anti-human leukocyte antigen (HLA) antibodies (dnDSAs). METHODS: A total of 584 KTx recipients were enrolled in this study, of whom 164 developed dnDSAs during the follow-up period and 420 did not. RESULTS: We found no significant relationship between TAC trough level during the follow-up period and dnDSA incidence. Patients who developed dnDSAs had a significantly greater number of HLA-A/B/DR mismatches (3.4 ± 1.3 versus 2.8 ± 1.5; P < 0.001), were more likely to have preformed DSAs (48.2% versus 27.1%; P < 0.001) and showed poor allograft outcome. CONCLUSIONS: There was no clear relationship between TAC trough level and dnDSA incidence for KTx recipients whose TAC trough levels were kept within the narrow range of 4–6 ng/mL during the immunosuppression maintenance period.
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spelling pubmed-81609582021-06-02 Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation Unagami, Kohei Ishida, Hideki Furusawa, Miyuki Kitajima, Kumiko Hirai, Toshihito Kakuta, Yoichi Toki, Daisuke Shimizu, Tomokazu Omoto, Kazuya Okumi, Masayoshi Nitta, Kosaku Tanabe, Kazunari Nephrol Dial Transplant Original Articles BACKGROUND: Tacrolimus (TAC) is a key immunosuppressant drug for kidney transplantation (KTx). However, the optimal serum trough level of TAC for good long-term outcomes remains unclear. This study aimed to investigate the relationship between the maintenance TAC trough level and the appearance of de novo donor-specific anti-human leukocyte antigen (HLA) antibodies (dnDSAs). METHODS: A total of 584 KTx recipients were enrolled in this study, of whom 164 developed dnDSAs during the follow-up period and 420 did not. RESULTS: We found no significant relationship between TAC trough level during the follow-up period and dnDSA incidence. Patients who developed dnDSAs had a significantly greater number of HLA-A/B/DR mismatches (3.4 ± 1.3 versus 2.8 ± 1.5; P < 0.001), were more likely to have preformed DSAs (48.2% versus 27.1%; P < 0.001) and showed poor allograft outcome. CONCLUSIONS: There was no clear relationship between TAC trough level and dnDSA incidence for KTx recipients whose TAC trough levels were kept within the narrow range of 4–6 ng/mL during the immunosuppression maintenance period. Oxford University Press 2020-12-05 /pmc/articles/PMC8160958/ /pubmed/33280052 http://dx.doi.org/10.1093/ndt/gfaa258 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Unagami, Kohei
Ishida, Hideki
Furusawa, Miyuki
Kitajima, Kumiko
Hirai, Toshihito
Kakuta, Yoichi
Toki, Daisuke
Shimizu, Tomokazu
Omoto, Kazuya
Okumi, Masayoshi
Nitta, Kosaku
Tanabe, Kazunari
Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title_full Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title_fullStr Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title_full_unstemmed Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title_short Influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
title_sort influence of a low-dose tacrolimus protocol on the appearance of de novo donor-specific antibodies during 7 years of follow-up after renal transplantation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160958/
https://www.ncbi.nlm.nih.gov/pubmed/33280052
http://dx.doi.org/10.1093/ndt/gfaa258
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