Systematic review and meta-analysis of cell therapy for COVID-19: global clinical trial landscape, published safety/efficacy outcomes, cell product manufacturing and clinical delivery

被引:22
作者
Couto, Pedro S. [1 ,2 ,3 ]
Al-Arawe, Nada [4 ,5 ,6 ,7 ,8 ]
Filgueiras, Igor S. [9 ]
Fonseca, Dennyson L. M. [10 ]
Hinterseher, Irene [8 ,11 ,12 ,13 ]
Catar, Rusan A. [4 ,5 ,6 ,7 ]
Chinnadurai, Raghavan [14 ]
Bersenev, Alexey [15 ]
Cabral-Marques, Otavio [9 ,10 ,16 ,17 ,18 ,19 ,20 ]
Moll, Guido [4 ,5 ,6 ,7 ,21 ]
Verter, Frances [2 ,3 ]
机构
[1] UCL, Adv Ctr Biochem Engn, Dept Biochem Engn, London, England
[2] CellTrials org, Brookeville, MD 20833 USA
[3] Parents Guide Cord Blood Fdn, Brookeville, MD 20833 USA
[4] Charite Univ Med Berlin, Dept Nephrol & Internal Intens Care Med, Berlin, Germany
[5] Free Univ Berlin, Berlin, Germany
[6] Humboldt Univ, Berlin, Germany
[7] Berlin Inst Hlth BIH, Berlin, Germany
[8] Charite Univ Med Berlin, Vasc Surg Clin, Berlin, Germany
[9] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, Sao Paulo, SP, Brazil
[10] Univ Sao Paulo, Inst Math & Stat IME, Interunit Postgrad Program Bioinformat, Sao Paulo, SP, Brazil
[11] Med Hsch Brandenburg Theodor Fontane, Univ Klinikum Ruppin Brandenburg, Dept Vasc Surg, Neuruppin, Germany
[12] Med Hsch Brandenburg Theodor Fontane, Univ Potsdam, Fak Gesundheitswissensch Brandenburg, Gemeinsame Fak, Potsdam, Germany
[13] Brandenburg Tech Univ BTU Cottbus Senftenberg, Potsdam, Germany
[14] Mercer Univ, Dept Biomed Sci, Sch Med, Savannah, GA USA
[15] Yale Sch Med, Adv Cell Therapy ACT Lab, New Haven, CT USA
[16] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Clin & Toxicol Anal, Sao Paulo, SP, Brazil
[17] Univ Fed Rio Grande do Norte, Dept Pharm, Natal, Brazil
[18] Univ Fed Rio Grande do Norte, Postgrad Program Hlth & Sci, Natal, Brazil
[19] Univ Sao Paulo, Dept Med, Div Mol Med, Sch Med, Sao Paulo, Brazil
[20] Univ Sao Paulo, Lab Med Invest 29, Sch Med, Sao Paulo, Brazil
[21] Charite Univ Med Berlin, Berlin Inst Hlth BIH, Ctr Regenerat Therapies BCRT, Berlin, Germany
基金
瑞典研究理事会;
关键词
cell and gene therapy (CGT); advanced therapy medicinal products (ATMPs); mesenchymal stromal; stem cells (MSCs); severe respiratory distress syndrome coronavirus 2 (SARS-CoV2); coronavirus induced disease 2019 (COVID-19); MESENCHYMAL STEM-CELLS; UMBILICAL-CORD BLOOD; STROMAL CELLS; BONE-MARROW; ADIPOSE-TISSUE; DIFFERENTIATION; INFUSION; PLACENTA;
D O I
10.3389/fimmu.2023.1200180
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页数:24
相关论文
共 149 条
[1]   The Systematic Effect of Mesenchymal Stem Cell Therapy in Critical COVID-19 Patients: A Prospective Double Controlled Trial [J].
Adas, G. ;
Cukurova, Z. ;
Yasar, K. Kart ;
Yilmaz, R. ;
Isiksacan, N. ;
Kasapoglu, P. ;
Yesilbag, Z. ;
Koyuncu, I. D. ;
Karaoz, E. .
CELL TRANSPLANTATION, 2021, 30
[2]   Human placenta-derived mesenchymal stem cells transplantation in patients with acute respiratory distress syndrome (ARDS) caused by COVID-19 (phase I clinical trial): safety profile assessment [J].
Aghayan, Hamid Reza ;
Salimian, Fatemeh ;
Abedini, Atefeh ;
Ghazi, Samrand Fattah ;
Yunesian, Masud ;
Alavi-Moghadam, Sepideh ;
Makarem, Jalil ;
Majidzadeh-A, Keivan ;
Hatamkhani, Ali ;
Moghri, Maryam ;
Danesh, Abbas ;
Haddad-Marandi, Mohammad Reza ;
Sanati, Hassan ;
Abbasvandi, Fereshteh ;
Arjmand, Babak ;
Azimi, Pourya ;
Ghavamzadeh, Ardeshir ;
Sarrami-Forooshani, Ramin .
STEM CELL RESEARCH & THERAPY, 2022, 13 (01)
[3]   Convergence of Cell Pharmacology and Drug Delivery [J].
Aijaz, Ayesha ;
Vaninov, Natalie ;
Allen, Ashley ;
Barcia, Rita N. ;
Parekkadan, Biju .
STEM CELLS TRANSLATIONAL MEDICINE, 2019, 8 (09) :874-879
[4]   Biomanufacturing for clinically advanced cell therapies [J].
Aijaz, Ayesha ;
Li, Matthew ;
Smith, David ;
Khong, Danika ;
LeBlon, Courtney ;
Fenton, Owen S. ;
Olabisi, Ronke M. ;
Libutti, Steven ;
Tischfield, Jay ;
Maus, Marcela V. ;
Deans, Robert ;
Barcia, Rita N. ;
Anderson, Daniel G. ;
Ritz, Jerome ;
Preti, Robert ;
Parekkadan, Biju .
NATURE BIOMEDICAL ENGINEERING, 2018, 2 (06) :362-376
[5]   Multi-Parameter Analysis of Biobanked Human Bone Marrow Stromal Cells Shows Little Influence for Donor Age and Mild Comorbidities on Phenotypic and Functional Properties [J].
Andrzejewska, Anastazja ;
Catar, Rusan ;
Schoon, Janosch ;
Qazi, Taimoor Hasan ;
Sass, Frauke Andrea ;
Jacobi, Dorit ;
Blankenstein, Antje ;
Reinke, Simon ;
Krueger, David ;
Streitz, Mathias ;
Schlickeiser, Stephan ;
Richter, Sarina ;
Souidi, Naima ;
Beez, Christien ;
Kamhieh-Milz, Julian ;
Krueger, Ulrike ;
Zemojtel, Tomasz ;
Juerchott, Karsten ;
Strunk, Dirk ;
Reinke, Petra ;
Duda, Georg ;
Moll, Guido ;
Geissler, Sven .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[6]   Mesenchymal stem cells: immune evasive, not immune privileged [J].
Ankrum, James A. ;
Ong, Joon Faii ;
Karp, Jeffrey M. .
NATURE BIOTECHNOLOGY, 2014, 32 (03) :252-260
[7]  
[Anonymous], 2022, OFF J EUR UN
[8]  
[Anonymous], REPAIR ACUTE RESP DI
[9]  
[Anonymous], Mesenchymal Stromal Cells For Acute Respiratory Distress Syndrome - Full Text View - ClinicalTrials.gov
[10]  
Ayatollahi M, 2016, IRAN J BASIC MED SCI, V19, P145