Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study

Abstract We investigated the clinical relevance of urinary cytokines/chemokines reflecting intrarenal immunologic micromilieu as prognostic markers and the optimal measurement timing after living donor kidney transplantation (LDKT). This prospective cohort study included 77 LDKT patients who were fo...

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Autores principales: Hye Ryoun Jang, Minjung Kim, Sungjun Hong, Kyungho Lee, Mee Yeon Park, Kyeong Eun Yang, Cheol-Jung Lee, Junseok Jeon, Kyo Won Lee, Jung Eun Lee, Jae Berm Park, Kyunga Kim, Ghee Young Kwon, Yoon Goo Kim, Dae Joong Kim, Wooseong Huh
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:3ea217acd66c4c8082e1eeef0d3f4a892021-12-02T15:15:23ZEarly postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study10.1038/s41598-021-98135-02045-2322https://doaj.org/article/3ea217acd66c4c8082e1eeef0d3f4a892021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-98135-0https://doaj.org/toc/2045-2322Abstract We investigated the clinical relevance of urinary cytokines/chemokines reflecting intrarenal immunologic micromilieu as prognostic markers and the optimal measurement timing after living donor kidney transplantation (LDKT). This prospective cohort study included 77 LDKT patients who were followed for ≥ 5 years. Patients were divided into control (n = 42) or acute rejection (AR, n = 35) group. Early AR was defined as AR occurring within 3 months. Serum and urine cytokines/chemokines were measured serially as follows: intraoperative, 8/24/72 h, 1 week, 3 months, and 1 year after LDKT. Intrarenal total leukocytes, T cells, and B cells were analyzed with immunohistochemistry followed by tissueFAXS. Urinary MCP-1 and fractalkine were also analyzed in a validation cohort. Urinary MCP-1 after one week was higher in the AR group. Urinary MCP-1, fractalkine, TNF-α, RANTES, and IL-6 after one week were significantly higher in the early AR group. Intrarenal total leukocytes and T cells were elevated in the AR group compared with the control group. Urinary fractalkine, MCP-1, and IL-10 showed positive correlation with intrarenal leukocyte infiltration. Post-KT 1 week urinary MCP-1 showed predictive value in the validation cohort. One-week post-KT urinary MCP-1 may be used as a noninvasive diagnostic marker for predicting AR after LDKT.Hye Ryoun JangMinjung KimSungjun HongKyungho LeeMee Yeon ParkKyeong Eun YangCheol-Jung LeeJunseok JeonKyo Won LeeJung Eun LeeJae Berm ParkKyunga KimGhee Young KwonYoon Goo KimDae Joong KimWooseong HuhNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hye Ryoun Jang
Minjung Kim
Sungjun Hong
Kyungho Lee
Mee Yeon Park
Kyeong Eun Yang
Cheol-Jung Lee
Junseok Jeon
Kyo Won Lee
Jung Eun Lee
Jae Berm Park
Kyunga Kim
Ghee Young Kwon
Yoon Goo Kim
Dae Joong Kim
Wooseong Huh
Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
description Abstract We investigated the clinical relevance of urinary cytokines/chemokines reflecting intrarenal immunologic micromilieu as prognostic markers and the optimal measurement timing after living donor kidney transplantation (LDKT). This prospective cohort study included 77 LDKT patients who were followed for ≥ 5 years. Patients were divided into control (n = 42) or acute rejection (AR, n = 35) group. Early AR was defined as AR occurring within 3 months. Serum and urine cytokines/chemokines were measured serially as follows: intraoperative, 8/24/72 h, 1 week, 3 months, and 1 year after LDKT. Intrarenal total leukocytes, T cells, and B cells were analyzed with immunohistochemistry followed by tissueFAXS. Urinary MCP-1 and fractalkine were also analyzed in a validation cohort. Urinary MCP-1 after one week was higher in the AR group. Urinary MCP-1, fractalkine, TNF-α, RANTES, and IL-6 after one week were significantly higher in the early AR group. Intrarenal total leukocytes and T cells were elevated in the AR group compared with the control group. Urinary fractalkine, MCP-1, and IL-10 showed positive correlation with intrarenal leukocyte infiltration. Post-KT 1 week urinary MCP-1 showed predictive value in the validation cohort. One-week post-KT urinary MCP-1 may be used as a noninvasive diagnostic marker for predicting AR after LDKT.
format article
author Hye Ryoun Jang
Minjung Kim
Sungjun Hong
Kyungho Lee
Mee Yeon Park
Kyeong Eun Yang
Cheol-Jung Lee
Junseok Jeon
Kyo Won Lee
Jung Eun Lee
Jae Berm Park
Kyunga Kim
Ghee Young Kwon
Yoon Goo Kim
Dae Joong Kim
Wooseong Huh
author_facet Hye Ryoun Jang
Minjung Kim
Sungjun Hong
Kyungho Lee
Mee Yeon Park
Kyeong Eun Yang
Cheol-Jung Lee
Junseok Jeon
Kyo Won Lee
Jung Eun Lee
Jae Berm Park
Kyunga Kim
Ghee Young Kwon
Yoon Goo Kim
Dae Joong Kim
Wooseong Huh
author_sort Hye Ryoun Jang
title Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
title_short Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
title_full Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
title_fullStr Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
title_full_unstemmed Early postoperative urinary MCP-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
title_sort early postoperative urinary mcp-1 as a potential biomarker predicting acute rejection in living donor kidney transplantation: a prospective cohort study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3ea217acd66c4c8082e1eeef0d3f4a89
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