Institute for Regenerative Medicine (IREM), Center for Therapy Development and Good Manufacturing Practice, University of Zurich, Zurich, Switzerland.
Scientific IT Services ETH Zurich, ETH Zurich, Zürich, Switzerland.
J Cell Mol Med. 2022 Jan;26(1):228-234. doi: 10.1111/jcmm.17048. Epub 2021 Nov 24.
The outbreak of COVID-19 has become a serious public health emergency. The virus targets cells by binding the ACE2 receptor. After infection, the virus triggers in some humans an immune storm containing the release of proinflammatory cytokines and chemokines followed by multiple organ failure. Several vaccines are enrolled, but an effective treatment is still missing. Mesenchymal stem cells (MSCs) have shown to secrete immunomodulatory factors that suppress this cytokine storm. Therefore, MSCs have been suggested as a potential treatment option for COVID-19. We report here that the ACE2 expression is minimal or nonexistent in MSC derived from three different human tissue sources (adipose tissue, umbilical cord Wharton`s jelly and bone marrow). In contrast, TMPRSS2 that is implicated in SARS-CoV-2 entry has been detected in all MSC samples. These results are of particular importance for future MSC-based cell therapies to treat severe cases after COVID-19 infection.
新型冠状病毒肺炎疫情已构成全球重大突发公共卫生事件。该病毒通过与 ACE2 受体结合而靶向细胞。感染后,病毒在一些人类中引发免疫风暴,导致促炎细胞因子和趋化因子的释放,随后发生多器官衰竭。目前已有多种疫苗在研发中,但仍缺乏有效的治疗方法。间充质干细胞(MSC)已被证明可分泌免疫调节因子,从而抑制这种细胞因子风暴。因此,MSC 已被提议作为 COVID-19 的一种潜在治疗选择。我们在此报告,源自三种不同人体组织来源(脂肪组织、脐带华通氏胶和骨髓)的 MSC 中 ACE2 的表达很少或不存在。相比之下,所有 MSC 样本中均检测到了参与 SARS-CoV-2 进入的 TMPRSS2。这些结果对于基于 MSC 的细胞疗法在 COVID-19 感染后治疗重症病例具有重要意义。