Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785057629462069248 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10259294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT biananning therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT yexiaoxue therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT wangjing therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT zengming therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT liujiayin therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT liukang therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT ningsong therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT cuiyugui therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT tangshaowen therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT xuxueqiang therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT yuanyanggang therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT suzhonglan therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT luyan therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT zhoujing therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT maxiang therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT yangguang therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT huangyaoyu therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT chenfeng therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT yuyoujia therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT gumufeng therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT lvxiaolin therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT wangling therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT zhaojing therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT wangxiuqin therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT liangningxia therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT xingchangying therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT qinlianju therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient AT wangningning therapeuticeffectsandmechanismofhumanamnionderivedmesenchymalstemcellsonhypercoagulabilityinauremiccalciphylaxispatient |