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Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient

Calciphylaxis is a rare cutaneous vascular disease that manifests with intolerable pains, non-healing skin wounds, histologically characterized by calcification, fibrointimal hyperplasia, and microvessel thrombosis. Currently, there are no standardized guidelines for this disease. Recent studies hav...

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Autores principales: Bian, Anning, Ye, Xiaoxue, Wang, Jing, Zeng, Ming, Liu, Jiayin, Liu, Kang, Ning, Song, Cui, Yugui, Tang, Shaowen, Xu, Xueqiang, Yuan, Yanggang, Su, Zhonglan, Lu, Yan, Zhou, Jing, Ma, Xiang, Yang, Guang, Huang, Yaoyu, Chen, Feng, Yu, Youjia, Gu, Mufeng, Lv, Xiaolin, Wang, Ling, Zhao, Jing, Wang, Xiuqin, Liang, Ningxia, Xing, Changying, Qin, Lianju, Wang, Ningning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259294/
https://www.ncbi.nlm.nih.gov/pubmed/37293809
http://dx.doi.org/10.1080/0886022X.2023.2218483
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author Bian, Anning
Ye, Xiaoxue
Wang, Jing
Zeng, Ming
Liu, Jiayin
Liu, Kang
Ning, Song
Cui, Yugui
Tang, Shaowen
Xu, Xueqiang
Yuan, Yanggang
Su, Zhonglan
Lu, Yan
Zhou, Jing
Ma, Xiang
Yang, Guang
Huang, Yaoyu
Chen, Feng
Yu, Youjia
Gu, Mufeng
Lv, Xiaolin
Wang, Ling
Zhao, Jing
Wang, Xiuqin
Liang, Ningxia
Xing, Changying
Qin, Lianju
Wang, Ningning
author_facet Bian, Anning
Ye, Xiaoxue
Wang, Jing
Zeng, Ming
Liu, Jiayin
Liu, Kang
Ning, Song
Cui, Yugui
Tang, Shaowen
Xu, Xueqiang
Yuan, Yanggang
Su, Zhonglan
Lu, Yan
Zhou, Jing
Ma, Xiang
Yang, Guang
Huang, Yaoyu
Chen, Feng
Yu, Youjia
Gu, Mufeng
Lv, Xiaolin
Wang, Ling
Zhao, Jing
Wang, Xiuqin
Liang, Ningxia
Xing, Changying
Qin, Lianju
Wang, Ningning
author_sort Bian, Anning
collection PubMed
description Calciphylaxis is a rare cutaneous vascular disease that manifests with intolerable pains, non-healing skin wounds, histologically characterized by calcification, fibrointimal hyperplasia, and microvessel thrombosis. Currently, there are no standardized guidelines for this disease. Recent studies have recognized a high prevalence of thrombophilias and hypercoagulable conditions in calciphylaxis patients. Here, we report a case of uremic calciphylaxis patient whom was refractory to conventional treatments and then received a salvage strategy with intravenous and local hAMSC application. In order to investigate the therapeutic mechanism of hAMSCs from the novel perspective of hypercoagulability, coagulation-related indicators, wound status, quality of life and skin biopsy were followed up. Polymerase chain reaction (PCR) was performed to determine the distribution of hAMSCs in multiple tissues including lung, kidney and muscle after infusion of hAMSCs for 24 h, 1 week and 1 month in mice aiming to investigate whether hAMSCs retain locally active roles after intravenous administration. Improvement of hypercoagulable condition involving correction of platelet, D-dimer and plasminogen levels, skin regeneration and pain alleviation were revealed after hAMSC administration over one-year period. Skin biopsy pathology suggested regenerative tissues after 1 month hAMSC application and full epidermal regeneration after 20 months hAMSC treatment. PCR analysis indicated that hAMSCs were homing in lung, kidney and muscle tissues of mice even until tail vein injection of hAMSCs for 1 month. We propose that hypercoagulability is a promising therapeutic target of calciphylaxis patients, which can be effectively improved by hAMSC treatment.
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spelling pubmed-102592942023-06-13 Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient Bian, Anning Ye, Xiaoxue Wang, Jing Zeng, Ming Liu, Jiayin Liu, Kang Ning, Song Cui, Yugui Tang, Shaowen Xu, Xueqiang Yuan, Yanggang Su, Zhonglan Lu, Yan Zhou, Jing Ma, Xiang Yang, Guang Huang, Yaoyu Chen, Feng Yu, Youjia Gu, Mufeng Lv, Xiaolin Wang, Ling Zhao, Jing Wang, Xiuqin Liang, Ningxia Xing, Changying Qin, Lianju Wang, Ningning Ren Fail Brief Report Calciphylaxis is a rare cutaneous vascular disease that manifests with intolerable pains, non-healing skin wounds, histologically characterized by calcification, fibrointimal hyperplasia, and microvessel thrombosis. Currently, there are no standardized guidelines for this disease. Recent studies have recognized a high prevalence of thrombophilias and hypercoagulable conditions in calciphylaxis patients. Here, we report a case of uremic calciphylaxis patient whom was refractory to conventional treatments and then received a salvage strategy with intravenous and local hAMSC application. In order to investigate the therapeutic mechanism of hAMSCs from the novel perspective of hypercoagulability, coagulation-related indicators, wound status, quality of life and skin biopsy were followed up. Polymerase chain reaction (PCR) was performed to determine the distribution of hAMSCs in multiple tissues including lung, kidney and muscle after infusion of hAMSCs for 24 h, 1 week and 1 month in mice aiming to investigate whether hAMSCs retain locally active roles after intravenous administration. Improvement of hypercoagulable condition involving correction of platelet, D-dimer and plasminogen levels, skin regeneration and pain alleviation were revealed after hAMSC administration over one-year period. Skin biopsy pathology suggested regenerative tissues after 1 month hAMSC application and full epidermal regeneration after 20 months hAMSC treatment. PCR analysis indicated that hAMSCs were homing in lung, kidney and muscle tissues of mice even until tail vein injection of hAMSCs for 1 month. We propose that hypercoagulability is a promising therapeutic target of calciphylaxis patients, which can be effectively improved by hAMSC treatment. Taylor & Francis 2023-06-09 /pmc/articles/PMC10259294/ /pubmed/37293809 http://dx.doi.org/10.1080/0886022X.2023.2218483 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Brief Report
Bian, Anning
Ye, Xiaoxue
Wang, Jing
Zeng, Ming
Liu, Jiayin
Liu, Kang
Ning, Song
Cui, Yugui
Tang, Shaowen
Xu, Xueqiang
Yuan, Yanggang
Su, Zhonglan
Lu, Yan
Zhou, Jing
Ma, Xiang
Yang, Guang
Huang, Yaoyu
Chen, Feng
Yu, Youjia
Gu, Mufeng
Lv, Xiaolin
Wang, Ling
Zhao, Jing
Wang, Xiuqin
Liang, Ningxia
Xing, Changying
Qin, Lianju
Wang, Ningning
Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title_full Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title_fullStr Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title_full_unstemmed Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title_short Therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
title_sort therapeutic effects and mechanism of human amnion-derived mesenchymal stem cells on hypercoagulability in a uremic calciphylaxis patient
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259294/
https://www.ncbi.nlm.nih.gov/pubmed/37293809
http://dx.doi.org/10.1080/0886022X.2023.2218483
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