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Mesenchymal stem cell treatment improves outcome of COVID-19 patients via multiple immunomodulatory mechanisms
- Zhu, Rongjia;
- Yan, Tingdong;
- Feng, Yingmei;
- Liu, Yan;
- Cao, Hongcui;
- ... Min, Kyung-Jin;
- 외 46명
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106SCOPUS
110초록
The infusion of coronavirus disease 2019 (COVID-19) patients with mesenchymal stem cells (MSCs) potentially improves clinical symptoms, but the underlying mechanism remains unclear. We conducted a randomized, single-blind, placebo-controlled (29 patients/group) phase II clinical trial to validate previous findings and explore the potential mechanisms. Patients treated with umbilical cord-derived MSCs exhibited a shorter hospital stay (P = 0.0198) and less time required for symptoms remission (P = 0.0194) than those who received placebo. Based on chest images, both severe and critical patients treated with MSCs showed improvement by day 7 (P = 0.0099) and day 21 (P = 0.0084). MSC-treated patients had fewer adverse events. MSC infusion reduced the levels of C-reactive protein, proinflammatory cytokines, and neutrophil extracellular traps (NETs) and promoted the maintenance of SARS-CoV-2-specific antibodies. To explore how MSCs modulate the immune system, we employed single-cell RNA sequencing analysis on peripheral blood. Our analysis identified a novel subpopulation of VNN2(+) hematopoietic stem/progenitor-like (HSPC-like) cells expressing CSF3R and PTPRE that were mobilized following MSC infusion. Genes encoding chemotaxis factors - CX3CR1 and L-selectin - were upregulated in various immune cells. MSC treatment also regulated B cell subsets and increased the expression of costimulatory CD28 in T cells in vivo and in vitro. In addition, an in vivo mouse study confirmed that MSCs suppressed NET release and reduced venous thrombosis by upregulating kindlin-3 signaling. Together, our results underscore the role of MSCs in improving COVID-19 patient outcomes via maintenance of immune homeostasis.
키워드
- 제목
- Mesenchymal stem cell treatment improves outcome of COVID-19 patients via multiple immunomodulatory mechanisms
- 저자
- Zhu, Rongjia; Yan, Tingdong; Feng, Yingmei; Liu, Yan; Cao, Hongcui; Peng, Gongxin; Yang, Yanlei; Xu, Zhen; Liu, Jingqi; Hou, Wei; Wang, Xiaoyue; Li, Zhe; Deng, Luchan; Wang, Shihua; Li, Jing; Han, Qin; Li, Hongling; Shan, Guangliang; Cao, Yinghao; An, Xingyan; Yan, Jianshe; Zhang, Zhonghui; Li, Huafei; Qu, Xuebin; Zhu, Jiaqi; Zhou, Shumin; Wang, Jiao; Zhang, Fengchun; Gao, Jinming; Jin, Ronghua; Xu, Dayong; Ma, Yan-Qing; Huang, Tao; Peng, Shuang; Zheng, Zhi; Stambler, Ilia; Gilson, Eric; Lim, Lee Wei; Moskalev, Alexey; Cano, Antonio; Chakrabarti, Sasanka; Ulfhake, Brun; Su, Huanxing; Xu, Haoying; Xu, Sihuan; Wei, Feng; Brown-Borg, Holly M.; Min, Kyung-Jin; Ellison-Hughes, Georgina; Caruso, Calogero; Jin, Kunlin; Zhao, Robert Chunhua
- 발행일
- 2021-12
- 유형
- Article
- 저널명
- Cell Research
- 권
- 31
- 호
- 12
- 페이지
- 1244 ~ 1262