AI Article Synopsis
- The study explored the long-term safety and effectiveness of human umbilical cord mesenchymal stem cells (hUC-MSCs) in severe COVID-19 patients over a one-year follow-up period.
- Significant improvements in pulmonary function were noted in both the hUC-MSCs group and the standard treatment group compared to earlier assessments, but fatigue persisted as a common issue.
- The hUC-MSCs group exhibited notably lower levels of certain biomarkers (KL-6 and MDA) compared to the control group without any apparent adverse effects, indicating a potentially beneficial treatment.
Article Abstract
Background: The novel coronavirus is still mutating, and the pandemic continues. Meanwhile, many COVID-19 survivors have residual postinfection clinical manifestations. Human umbilical cord mesenchymal stem cells (hUC-MSCs) have been shown to be effective in the early stages of COVID-19.
Objectives: The aim of this study was to investigate long-term safety and efficacy of treatment in patients with severe COVID-19 patients who had received hUC-MSCs therapy.
Methods: Twenty-five discharged patients who had severe COVID-19 (including the standard treatment group and the standard treatment plus hUC-MSCs group) were enrolled in a 1-year follow-up. The assessment considered adverse effects (including effects on liver and kidney function, coagulation, ECG, tumor marker, and so on), pulmonary function, St George's Respiratory Questionnaire (SGRQ), postinfection sequelae and serum concentration of Krebs von den Lungen-6 (KL-6), malondialdehyde (MDA), HS, carnitine, and N-6 long-chain polyunsaturated fatty acids (N-6 LC-PUFAs).
Measurements And Main Results: Pulmonary ventilation function had significantly improved at the 1-year follow-up in both the hUC-MSCs group and the control group compared with the 3-month follow-up (P < 0.01). Fatigue (60% [15/25]) remained the most common symptom at the 1-year follow-up. The rate of fatigue relief was significantly reduced in the hUC-MSCs group (25% [2/8]) compared to the control group (76.5% [13/17]) (P = 0.028). The level of KL-6 was significantly lower in the hUC-MSCs group (2585.5 ± 186.5 U/ml) than in the control group (3120.7 ± 158.3 U/ml) (P < 0.001). Compared with the control group, the hUC-MSCs group had a lower level of MDA (9.27 ± 0.54 vs. 9.91 ± 0.72 nmol/ml, P = 0.036). No obvious adverse effects were observed in the hUC-MSCs treatment group at 1 year after discharge.
Conclusions: Intravenous transplantation of hUC-MSCs was a safe approach in the long term in the treatment of patients with severe COVID-19. In addition, hUC-MSCs had a positive effect on postinfection sequelae in COVID-19 survivors.
Trial Registration: Chinese Clinical Trial Registration; ChiCTR2000031494; Registered 02 April 2020-Retrospectively registered, http://www.medresman.org.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288258 | PMC |
| http://dx.doi.org/10.1186/s13287-022-02972-3 | DOI Listing |
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