ATMP-classified, scalable, autologous cell spray for the treatment of skin wounds and assessment of its effects on wound healing clinically and on a molecular level

被引:5
作者
Nuutila, Kristo [1 ]
Katayama, Shintaro [2 ,3 ,4 ]
Laitinen, Anita [5 ]
Siltanen, Antti [6 ]
Patrikoski, Mimmi [5 ]
Valtonen, Jussi [7 ,8 ]
Kankainen, Matti [9 ,10 ,11 ]
Kerkelae, Erja [5 ]
Kaartinen, Tanja [5 ]
Juteau, Susanna [12 ]
Korhonen, Matti [5 ]
Vuola, Jyrki [7 ,8 ]
Kankuri, Esko [6 ]
机构
[1] US Army, Inst Surg Res, Ft Sam Houston, TX USA
[2] Res Ctr, Helsinki, Finland
[3] Univ Helsinki, Fac Med, STEMM Res Program, Helsinki, Finland
[4] Karolinska Inst, Dept Biosci & Nutr, Huddinge, Sweden
[5] Adv Cell Therapy Ctr, Finnish Red Cross Blood Serv, Helsinki, Finland
[6] Univ Helsinki, Fac Med, Dept Pharmacol, POB 63,Haartmaninkatu 8, Helsinki 00014, Finland
[7] Univ Helsinki, Helsinki Burn Ctr, Dept Plast Surg, Helsinki, Finland
[8] Helsinki Univ Hosp, Helsinki, Finland
[9] Univ Helsinki, Helsinki Univ Hosp, Med & Clin Genet, Helsinki, Finland
[10] Univ Helsinki, Translat Immunol Res Program, Helsinki, Finland
[11] Univ Helsinki, Dept Clin Chem, Helsinki, Finland
[12] Univ Helsinki, Dept Pathol, Helsinki, Finland
关键词
Burns; Cell therapy; Epithelialization; Keratinocytes; Skin wound healing; Transcriptome; MICROGRAFT TRANSPLANTATION; EVOLUTION; EFFICACY; GRAFTS;
D O I
10.1016/j.burns.2022.09.006
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Autologous split-thickness skin grafts (STSGs) are the standard of care for closure of deep and large burns. However, perforation and extensive fishnet-like expansion of the grafts to achieve greater area wound coverage can lead to treatment failures or esthetically poor healing outcomes and scarring. The purpose of this study was to validate an autologous advanced therapy medicinal product (ATMP)-compliant skin cell suspension and evaluate its efficacy to promote epithelialization.Methods: Cells isolated from a piece of STSG according to ATMP classification requirements were sprayed onto 20 patients during a single operation in a validation study. Comparative evaluation of treatment efficacy was carried out using side-by-side skin graft donor site wounds that were standardized in depth. Firstly, we characterized wound healing transcriptomes at 14 and 21 days from serial wound biopsies in seven patients. Then, side-by side wounds in four patients were treated with or without the skin cells. The wounds were photographed, clinical outcomes assessed, and the treatment and control wound transcriptomes at 14 days were compared to the untreated wounds' healing transcriptomes.Results: The average cell yield after isolation from the STSG was 2.4 x 106 cells/cm2 with 96 % viability. The product contained mainly keratinocytes and their precursors but also other skin cells such as fibroblasts were present. As compared to vehicle-treated donor site wounds, the wounds treated with cells demonstrated improved epithelialization by both direct comparison and machine learning analysis of the transcriptomes.Conclusions: We showed that rapid and scalable ATMP-classified processing of skin cells is feasible, and application of the skin cells effectively promotes healing and epithelization of donor site wounds.& COPY; 2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:1144 / 1156
页数:13
相关论文
共 40 条
[1]  
Alrubaiy Laith, 2009, Oman Med J, V24, P4, DOI 10.5001/omj.2009.2
[2]   Cultured epithelial autograft (CEA) in burn treatment: Three decades later [J].
Atiyeh, Bishara S. ;
Costagliola, Michel .
BURNS, 2007, 33 (04) :405-413
[3]   A systematic review and meta-analysis of randomized trials evaluating the efficacy of autologous skin cell suspensions for re-epithelialization of acute partial thickness burn injuries and split-thickness skin graft donor sites [J].
Bairagi, Anjana ;
Griffin, Bronwyn ;
Banani, Tara ;
McPhail, Steven M. ;
Kimble, Roy ;
Tyack, Zephanie .
BURNS, 2021, 47 (06) :1225-1240
[4]  
Billard MJ, 2014, AM J CLIN EXP IMMUNO, V3, P97
[5]   The Fibroblast Integrin α11β1 Is Induced in a Mechanosensitive Manner Involving Activin A and Regulates Myofibroblast Differentiation [J].
Carracedo, Sergio ;
Lu, Ning ;
Popova, Svetlana N. ;
Jonsson, Roland ;
Eckes, Beate ;
Gullberg, Donald .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (14) :10434-10445
[6]   PERMANENT COVERAGE OF LARGE BURN WOUNDS WITH AUTOLOGOUS CULTURED HUMAN EPITHELIUM [J].
GALLICO, GG ;
OCONNOR, NE ;
COMPTON, CC ;
KEHINDE, O ;
GREEN, H .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (07) :448-451
[7]   A randomized trial comparing ReCell® system of epidermal cells delivery versus classic skin grafts for the treatment of deep partial thickness burns [J].
Gravante, G. ;
Di Fede, M. C. ;
Araco, A. ;
Grimaldi, M. ;
De Angelis, B. ;
Arpino, A. ;
Cervelli, V. ;
Montone, A. .
BURNS, 2007, 33 (08) :966-972
[8]   Management of Burns [J].
Greenhalgh, David G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (24) :2349-2359
[9]   Epidermal Regeneration by Micrograft Transplantation with Immediate 100-Fold Expansion [J].
Hackl, Florian ;
Bergmann, Juri ;
Granter, Scott R. ;
Koyama, Taro ;
Kiwanuka, Elizabeth ;
Zuhaili, Baraa ;
Pomahac, Bohdan ;
Caterson, Edward J. ;
Junker, Johan P. E. ;
Eriksson, Elof .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2012, 129 (03) :443E-452E
[10]   Eschar removal by bromelain based enzymatic debridement (Nexobrid®) in burns: European consensus guidelines update [J].
Hirche, Christoph ;
Almeland, Stian Kreken ;
Dheansa, Baljit ;
Fuchs, Paul ;
Governa, Maurizio ;
Hoeksema, Henk ;
Korzeniowski, Tomasz ;
Lumenta, David B. ;
Marinescu, Silviu ;
Ramon Martinez-Mendez, Jose ;
Plock, Jan A. ;
Sander, Frank ;
Ziegler, Benjamin ;
Kneser, Ulrich .
BURNS, 2020, 46 (04) :782-796