Department of Biochemical Engineering, Advanced Centre for Biochemical Engineering, University College London, London, United Kingdom.
CellTrials.org and Parent's Guide to Cord Blood Foundation, a non-profit organization headquartered in Brookeville, Brookeville, MD, United States.
Front Immunol. 2023 Jun 21;14:1200180. doi: 10.3389/fimmu.2023.1200180. eCollection 2023.
During the pandemic of severe respiratory distress syndrome coronavirus 2 (SARS-CoV2), many novel therapeutic modalities to treat Coronavirus 2019 induced disease (COVID-19) were explored. This study summarizes 195 clinical trials of advanced cell therapies targeting COVID-19 that were registered over the two years between January 2020 to December 2021. In addition, this work also analyzed the cell manufacturing and clinical delivery experience of 26 trials that published their outcomes by July 2022. Our demographic analysis found the highest number of cell therapy trials for COVID-19 was in United States, China, and Iran (N=53, 43, and 19, respectively), with the highest number per capita in Israel, Spain, Iran, Australia, and Sweden (N=0.641, 0.232, 0,223, 0.194, and 0.192 trials per million inhabitants). The leading cell types were multipotent mesenchymal stromal/stem cells (MSCs), natural killer (NK) cells, and mononuclear cells (MNCs), accounting for 72%, 9%, and 6% of the studies, respectively. There were 24 published clinical trials that reported on infusions of MSCs. A pooled analysis of these MSC studies found that MSCs provide a relative risk reduction for all-cause COVID-19 mortality of RR=0.63 (95% CI 0.46 to 0.85). This result corroborates previously published smaller meta-analyses, which suggested that MSC therapy demonstrated a clinical benefit for COVID-19 patients. The sources of the MSCs used in these studies and their manufacturing and clinical delivery methods were remarkably heterogeneous, with some predominance of perinatal tissue-derived products. Our results highlight the important role that cell therapy products may play as an adjunct therapy in the management of COVID-19 and its related complications, as well as the importance of controlling key manufacturing parameters to ensure comparability between studies. Thus, we support ongoing calls for a global registry of clinical studies with MSC products that could better link cell product manufacturing and delivery methods to clinical outcomes. Although advanced cell therapies may provide an important adjunct treatment for patients affected by COVID-19 in the near future, preventing pathology through vaccination still remains the best protection to date. We conducted a systematic review and meta-analysis of advanced cell therapy clinical trials as potential novel treatment for COVID-19 (resulting from SARS-CoV-2 coronavirus infection), including analysis of the global clinical trial landscape, published safety/efficacy outcomes (RR/OR), and details on cell product manufacturing and clinical delivery. This study had a 2-year observation interval from start of January 2020 to end of December 2021, including a follow-up period until end of July to identify published outcomes, which covers the most vivid period of clinical trial activity, and is also the longest observation period studied until today. In total, we identified 195 registered advanced cell therapy studies for COVID-19, employing 204 individual cell products. Leading registered trial activity was attributed to the USA, China, and Iran. Through the end of July 2022, 26 clinical trials were published, with 24 out of 26 articles employing intravenous infusions (IV) of mesenchymal stromal/stem cell (MSC) products. Most of the published trials were attributed to China and Iran. The cumulative results from the 24 published studies employing infusions of MSCs indicated an improved survival (RR=0.63 with 95% Confidence Interval 0.46 to 0.85). Our study is the most comprehensive systematic review and meta-analysis on cell therapy trials for COVID-19 conducted to date, clearly identifying the USA, China, and Iran as leading advanced cell therapy trial countries for COVID-19, with further strong contributions from Israel, Spain, Australia and Sweden. Although advanced cell therapies may provide an important adjunct treatment for patients affected by COVID-19 in the future, preventing pathology through vaccination remains the best protection.
在严重呼吸窘迫综合征冠状病毒 2(SARS-CoV2)大流行期间,探索了许多治疗 2019 年冠状病毒病(COVID-19)的新型治疗方法。本研究总结了 2020 年 1 月至 2021 年 12 月期间登记的 195 项针对 COVID-19 的先进细胞治疗临床试验。此外,这项工作还分析了截至 2022 年 7 月发表结果的 26 项试验的细胞制造和临床输送经验。我们的人口统计学分析发现,针对 COVID-19 的细胞治疗试验数量最多的国家是美国、中国和伊朗(分别为 53、43 和 19 项),人均数量最多的国家是以色列、西班牙、伊朗、澳大利亚和瑞典(分别为每百万居民 0.641、0.232、0、0.223、0.194 和 0.192 项)。领先的细胞类型是多能间充质基质/干细胞(MSCs)、自然杀伤(NK)细胞和单核细胞(MNCs),分别占研究的 72%、9%和 6%。有 24 项已发表的临床试验报告了 MSCs 的输注。对这些 MSC 研究的汇总分析发现,MSC 为全因 COVID-19 死亡率提供了相对风险降低,RR=0.63(95%CI 0.46 至 0.85)。这一结果与之前发表的较小的荟萃分析结果一致,这些分析表明 MSC 治疗对 COVID-19 患者具有临床益处。这些研究中使用的 MSC 的来源及其制造和临床输送方法差异很大,一些以围产期组织衍生产品为主。我们的研究结果强调了细胞治疗产品在 COVID-19 及其相关并发症管理中可能作为辅助治疗的重要作用,以及控制关键制造参数以确保研究之间可比性的重要性。因此,我们支持目前正在呼吁建立一个包含 MSC 产品的临床研究全球注册,这可以更好地将细胞产品制造和输送方法与临床结果联系起来。尽管先进的细胞疗法可能在不久的将来为受 COVID-19 影响的患者提供一种重要的辅助治疗方法,但通过接种疫苗预防病理仍然是迄今为止最好的保护措施。我们对高级细胞治疗临床试验作为 SARS-CoV-2 冠状病毒感染引起的 COVID-19 的潜在新型治疗方法进行了系统评价和荟萃分析,包括分析全球临床试验格局、发表的安全性/疗效结果(RR/OR),以及细胞产品制造和临床输送的详细信息。这项研究的观察间隔为 2020 年 1 月开始至 2021 年 12 月结束,包括到 2022 年 7 月底的随访期,以确定已发表的结果,这涵盖了临床试验活动最活跃的时期,也是迄今为止研究的最长观察期。总共确定了 195 项针对 COVID-19 的已注册高级细胞治疗研究,采用了 204 种不同的细胞产品。主要的注册试验活动归因于美国、中国和伊朗。截至 2022 年 7 月底,已有 26 项临床试验发表,其中 24 项文章采用静脉输注(IV)间充质基质/干细胞(MSC)产品。发表的大多数试验都来自中国和伊朗。对 24 项发表的输注 MSC 研究的累积结果表明,生存率得到改善(RR=0.63,95%置信区间为 0.46 至 0.85)。本研究是迄今为止针对 COVID-19 进行的细胞治疗试验最全面的系统评价和荟萃分析,明确确定了美国、中国和伊朗是 COVID-19 的主要先进细胞治疗试验国家,以色列、西班牙、澳大利亚和瑞典也做出了强有力的贡献。尽管先进的细胞疗法在未来可能为受 COVID-19 影响的患者提供一种重要的辅助治疗方法,但通过接种疫苗预防病理仍然是最好的保护措施。