Phase 1 trial for treatment of COVID‐19 patients with pulmonary fibrosis using hESC‐IMRCs

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Abstract

To the Editor: Pulmonary fibrosis is a severe complication in COVID-19 patients. Based on our previous success with stem cell therapy of acute lung injury in mouse models and 2 COVID-19 patients in a pilot compassionate use study,1 we describe a Phase 1 clinical trial where we treated COVID-19 patients with pulmonary fibrosis using human embryonic stem cell–derived immunity- and matrix-regulatory cells (hESC-IMRCs) during the SARS-CoV-2 outbreak in Wuhan City. Based on our recruitment criteria, we identified 27 COVID-19 patients who demonstrated pulmonary fibrosis pathology (Figure S1). All subjects had remained SARS-CoV-2–positive for more than three weeks. The median age of the patients was 66.5 years, of which 70% were men (Table 1). Patients with confirmed COVID-19 were diagnosed with pulmonary fibrosis using chest CT scans. A total of 20 patients were inpatients, while the other 7 subjects were discharged patients who still presented respiratory symptoms due to pulmonary fibrosis. Of the 20 inpatients, 10 were classified as severe/critical cases while another 10 were classified as moderate cases. Of the 20 inpatients who had pulmonary fibrosis and experienced shortness of breath at rest or exercise, 16 of 20 were supported by continuous oxygen therapy, of whom 1 depended on high-flow oxygen therapy. Another 4 of 20 inpatients also had pulmonary fibrosis and various respiratory symptoms, but only needed oxygen therapy after exercise. The 7 discharged patients presented respiratory symptoms only when they walked quickly. Total (N = 27) Severe/Critical inpatients (N = 10) Moderate inpatients (N = 10) Discharged patients (N = 7) After obtaining informed consent and approval, all 27 patients received intravenous transfusion of hESC-IMRCs at a dose of 3 × 106 cells/kg of body weight. 25 of the 27 patients received intravenous transfusion of hESC-IMRCs twice, whereas the other 2 patients received intravenous infusion of hESC-IMRCs once and thrice, respectively. The patient who received three hESC-IMRC infusions was classified as a moderate case. His clinical symptoms had disappeared 10 days after the first hESC-IMRC infusion, but remained SARS-CoV-2–positive until 28 days after treatment, upon which he was discharged. We proceeded to follow up with all the patients 84 days after the first hESC-IMRC treatment by either re-examination within the hospital or interviews over the phone. The 7 discharged patients could exercise with moderate intensity without significant symptoms upon 56 days after the hESC-IMRC treatment. Their lung fibrotic lesion areas had significantly decreased as observed from their chest CT scans (Figure S1C). We collected chest CT images from 3 of the 20 inpatients 7 days after treatment (Figure S1A-B, Patients #5, #20 and #22). The chest CT images also showed that their fibrosis lesions had improved. Chest CT scans were performed for 2 of the 20 inpatients 28 days after hESC-IMRC infusion, and their lung fibrotic lesion areas were also found to have decreased significantly (Figure S1A, Patient #10, #23). One of the 20 inpatients was dropped due to withdrawal of consent from the family. For the remaining 14 of 20 inpatients, their lung fibrotic lesion areas were also significantly diminished by 84 days after treatment (Figure S1). None of the treated patients suffered any adverse events or abnormal responses related to cell therapy. All haematological and clinical chemistry parameters remained in the normal range (Table S1). In addition, no tumour markers were detected in the serum, demonstrating that hESC-IMRCs were safe for intravenous infusion. In this series of COVID-19 patients with pulmonary fibrosis, there were demonstrable improvements in many clinical symptoms within a short period after hESC-IMRC transfusion (Table 1). Our cell therapy for lung fibrosis is safe for subjects in the medium term, for up to 84 days. Long-term safety will be observed in long-term follow-up at a later stage. Due to the special emergency presented by the COVID-19 outbreak in Wuhan, it should be noted that 7 of the 10 severe/critical cases had already undergone other clinical trials and 28 days of follow-up prior to this Phase 1 trial, but had still remained positive for pulmonary fibrosis. However, 27 of 27 patients displayed clinical improvements within 84 days after treatment with our hESC-IMRC therapy. In this Phase 1 trial, we have demonstrated that hESC-IMRCs are safe for intravenous infusion in the medium term, and our preliminary results showed efficacy for pulmonary fibrosis in COVID-19 patients. In order to further evaluate the clinical efficacy of this approach, we are now performing a multicentre randomized placebo-controlled Phase 2/3 trial. This work was supported by the National Key Research and Development Program (2020YFC0843900, 2020YFC0841900, 2018YFA0108400, 2017YFA0104403, 2016YFA0101502 and 2017YFA0105003), Beijing Municipal Science & Technology Commission (Z181100003818005), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA16030601, XDA16030403 and XDA16040502), the National Natural Science Foundation of China (31621004), the Key Research Projects of the Frontier Science of the Chinese Academy of Sciences (QYZDY-SSW-SMC002) and International Partnership Program of Chinese Academy of Sciences (152111KYSB20160004). The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported. BH, XW and JH conceived the project. ZL, TG and BG provided the testing results of IMRCs. TL, FJ, XZ and WL analysed clinical case. JW, XZ, YT and LW designed the research and wrote the manuscript with help from all of the authors. JW, XZ, YT and LW contributed equally to this letter. BH, XW and J.H are the corresponding authors of this letter. All authors read and approved the final manuscript. The study is approved by the Ethics Committee of Jinyintan Hospital, Wuhan, China. This clinical trial was registered with the National Medical Products Administration of China. The data that support the findings of this study are available from the corresponding author upon reasonable request. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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