Cadaveric bone marrow mesenchymal stem cells: first experience treating a patient with large severe burns
- Eduardo Mansilla1Email author,
- Gustavo H. Marín1,
- Mirta Berges2,
- Silvia Scafatti2,
- Jaime Rivas2,
- Andrea Núñez2,
- Martin Menvielle2,
- Roberto Lamonega2,
- Cecilia Gardiner2,
- Hugo Drago3,
- Flavio Sturla3,
- Mercedes Portas3,
- Silvia Bossi3,
- Maria Victoria Castuma1,
- Sandra Peña Luengas4,
- Gustavo Roque1,
- Karina Martire1,
- Jose Maria Tau1,
- Gabriel Orlandi1 and
- Adrian Tarditti1
© The Author(s) 2015
Received: 9 June 2015
Accepted: 5 September 2015
Published: 18 September 2015
In January 2005, Rasulov et al. originally published “First experience in the use of bone marrow mesenchymal stem cells (MSCs) for the treatment of a patient with deep skin burns”. Here, we present the first ever treated patient with cadaveric bone marrow mesenchymal stem cells (CMSCs) in the history of Medicine.
A young man, who severely burned 60 % of his total body surface with 30 % of full-thickness burns while working with a grass trimmer that exploded, was involved in the study. MSCs were obtained from the bone marrow of a cadaver donor in a routine procurement procedure of CUCAIBA, the Province of Buenos Aires, Argentina, Ministry of Health, Transplantation Agency, cultured, expanded, and applied on the burned surfaces using a fibrin spray after early escharotomy.
So far, our preliminary experience and our early results have been very impressive showing an outstanding safety data as well as some impressive good results in the use of CMSCs.
Based on all this, we think that improvements in the use of stem cells for burns might be possible in the near future and a lot of time as well as many lives could be saved by many other research teams all over the world. CMSCs will probably be a real scientific opportunity in Regenerative Medicine as well as in Transplantation.
KeywordsBurns Cadaveric Transplantation Skin regeneration Mesenchymal stem cells
In January 2005, Rasulov et al. originally published “First experience in the use of bone marrow mesenchymal stem cells (MSCs) for the treatment of a patient with deep skin burns”. This was the first treatment in the history of medicine that used allogeneic MSCs in a human being with extensive skin burns [superficial to full-thickness skin burn, total area 40 %, full-thickness burn area 30 %]. “Allogeneic fibroblast-like bone marrow MSCs,” as designated at that time by the authors, were placed onto the surface of a deep and large thermal burn of a female patient. The dynamic of healing confirmed a high tempo of wound regeneration in the presence of active neo-angiogenesis after transplantation of these “fibroblast-like MSCs”. Due to this, auto-dermoplasty of the burn wounds could be carried out with good results as early as on day 4 after transplantation of the stem cells, leading to a more rapid healing of the donor zones and an accelerated rehabilitation of the patient . During that same month of January 2005, we published “Human mesenchymal stem cells are tolerized by mice and improve skin and spinal cord injuries,” in which we presented an accelerated healing process of injured mice skins and spinal cords obtained by the use of xenogeneic (human to mice) MSCs. In this way, immunological barriers were trespassed beyond species without no rejection or adverse reactions to the transplanted human stem cells or the mice, respectively, with very good clinical results . In 2006, we found and described for the first time, “Bloodstream cells phenotypically identical to human mesenchymal bone marrow stem cells circulating in large amounts under the influence of acute large skin damage”. This was without any doubt, a new and paradigmatic evidence for the future use of these cells in regenerative medicine procedures, specially for the treatment of human large burns. We also originally proposed in this paper that it could be possible to mobilize MSCs from the bone marrow by induced therapeutic ways. These pharmacological mechanisms could be very similar to those biochemical alarm signals, naturally produced from damaged tissues, in order to accomplish many regenerative mechanisms . In December 2010, we observed and published an “Outstanding survival and regeneration process by the use of intelligent acellular dermal matrices and MSCs”. This study was done in a burned pig model in which an “intelligent” acellular biological pig dermis with nanoparticles and fibers coated with an anti-CD44 monoclonal antibody and loaded with growth factors like GM-CSF were implanted in a deep severe wound bed after escharotomy of the burned tissue . In 2011, we presented to our Argentine regulatory authority for organ, tissue and cell transplantation (INCUCAI) the first clinical trial protocol ever being designed in the world using cadaveric bone marrow mesenchymal stem cells (CMSCs) for the treatment of large burns. This was communicated in an editorial to Burns: “Time and regeneration in burns treatment: heading into the first worldwide clinical trial with cadaveric mesenchymal stem cells”, in which we made special considerations about the importance of time in the accomplishment of the regeneration processes of wound healing, specially when stem cells are used . As this trial was approved (including the INCUCAI Ethic Committee review process and the signed consent form), we treated the first patient by the end of that year. CMSCs will probably be a real scientific opportunity in Regenerative Medicine as well as in Transplantation . We were the first research group in the world to use them for regenerative purposes [5, 7]. There is still a great potential in these cells to be discovered. They might significantly change in the near future the possible sources for stem cells obtention. CMSCs could be very important tools to treat burns as well as many other diseases [8–14]. By now, we have made just a little advance in this new field of regenerative medicine by using CMSCs for the treatment of large and deep burns. Here, we present the first experience in the world with this kind of cell treatment applied to a severe burned patient after more than 3 years of follow-up.
Obtention and preparation of human CMSCs for transplantation
Bone marrow blood was obtained by needle aspiration from the iliac bone of a unique cadaver donor, in a routine procurement procedure of our Province of Buenos Aires, Argentina, Ministry of Health, Transplantation Agency, CUCAIBA, after cardiac arrest and when all other organs and tissues for transplantation were already collected. In this procurement procedure, the donor was selected by his negative tests for all adventitious agents, including hepatitis B and C, AIDS, syphilis, cytomegalovirus, and chagas, among many others, as needed by law, for organ and tissue transplantation. Briefly, 10 ml of heparinized bone marrow blood was sterile and transported to our Tissue Engineering, Regenerative Medicine, and Cell Therapies Laboratory in La Plata, Argentina, and processed in a clean room under sterile and GMP conditions. Each 2 ml of this bone marrow blood was diluted in 15 ml of low-glucose DMEM (Gibco/Life Technologies) and cultured for the isolation of MSC in 75 cm2 tissue culture flasks at 37 °C in a 5 % CO2 incubator at 95 % humidity with 10 % human platelet lysate (HPL) obtained from platelet-rich plasma procured by our Province of Buenos Aires Blood Bank. Few MSCs cells were present in the initial inoculum, but after culture, they expanded rapidly exponentially. MSCs appeared soon as typical round colonies, and a monolayer started to form over 14–17 days. When an 80 % of confluence was obtained, MSCs were detached from the culture flasks, expanded in a second passage, phenotyped as CD105-, CD73-, CD44-, and CD90-positive cells, lacking CD45, CD34, CD14, CD11b, CD79, CD19, and HLA-DR surface molecules expression, microbiologically tested, karyotyped as normal, and cryopreserved as needed. Cultured cells were daily examined under a phase contrast inverted microscope. The final samples before implantation were always negative as tested for adventitious agents, and small amounts of all of them were kept in quarantine for a period of time after transplantation. There is not clearly a certain or definitive amount of cells yet to be used in these procedures, and the selected concentration for this trial was based in previous work done by us in animal studies and data presented by others before in different reports. A final suspension of MSCs at a concentration of 1 × 106 cells/ml was prepared from the adherent cells in the plastic flasks and mixed in a fraction of cryoprecipitate from donor blood, with high amounts of fibrinogen and other clotting factors, obtained from the same blood bank as the HPL. A second component was also prepared with thrombin (Tissucol, Baxter) at a concentration of 5 U/ml of PBS.
Repairment of burn wound with CMSCs
Both solutions as mentioned in the “Obtention and preparation of human cadaveric MSCs for transplantation” section, one with the fibrinogen and MSCs and the other one with thrombin, were introduced and preserved in two different sterile conical tubes at room temperature, transported within the next hour to the Burns Unit at the San Martín Hospital of the Province of Buenos Aires, Ministry of Health in La Plata, Argentina, and sprayed onto the burn wound surface of the patient after deep escharotomy at a density of 1 × 106 MSCs per 100 cm2, using a “duplo-jet” system. In this way, thrombin polymerized the fibrinogen of the cryoprecipitate fraction and adhered the cells within a friendly fibrin matrix to the injured surface immediately as it was sprayed over the wounded area. After cell transplantation, the burned surfaces were dressed with a sterile polymeric transparent film that was first changed on day 7 and every other 2/3 days later on. A total of two main courses of this kind of cell therapy were administered to the wounded areas with 2-week difference between each other. Wound healing process and efficacy of the cell therapy was evaluated visually during wound observation on days 1, 3, 6, 7, 9, 11, and 13 and then as needed. As we focused on the question of stem cell persistence and its detection in the treated wound bed after its implantation, we decided for practical methodology and ethical reasons not to do so in this moment besides that it could have been a great idea to finally elucidate MSC fate and possible differentiation times and pathways when they have been transplanted in a human being from an allogeneic source as our cadaver donor. Also, as there is no evidence of immunological rejection events by using allogeneic MSCs, we have designed our procedure using CMSCs without the need of HLA matching between the donor and recipient. Anyway, we performed HLA typification of both the donor and the patient’s cells. Also, we looked for microchimerism  as well as any possible adverse effect related to immune intolerance or rejection. It is very important to emphasize that we were ready to document any possible adverse effect at any time, with safety as being one of the main end points of the trial. We have used as control group all patients with similar type of skin lesions treated in our Burn Unit with standard therapies in the past 10 years. Our efficacy end points were mortality rate, days to complete healing of the lesions, hospitalized total days, amount of surgery procedures performed, functional sequelae, quality of the regenerated skin, and infectious complications, among many others. As this is only one patient presented here, a statistical analysis was not carried on yet to see the differences in wound healing between CMSC-treated wounds and non-CMSC-treated wounds.
Similarity of results obtained in this study and by Rasulov’s group
Our results seem to be very similar to those described by the Rasulov’s group . Both, Rasulov and us, have seen an interesting fasting growth not only of a “granulating dermal-like” tissue but also of a limited new epidermis mainly from the wound edges. At the same time, local infection or necrosis do not seem to be big concerns while using this type of therapy. There was a rapid development of neo-angiogenesis in the lesions treated with MSCs with a simultaneous growth of a granulation-like tissue. Surprisingly, all these surfaces never showed any sign of infection or necrosis. Incipient epithelialization was observed by us soon after the first week of CMSC implantation, may be induced by the capacity of these allogeneic CMSCs to promote epithelial and endothelial growth mainly as it was said before at the periphery of the wounds, decreasing the total burned area. Also, healing by fast epithelial growth was observed inside the meshed spaces of the AMSGs. In further evaluations of the treated deep wounds, limited hair regrowth was observed in some areas. We have seen and described similar results in our burned pig model . Rasulov’s and our patient needed a final epithelium replacement as it was described. We used AMSGs while the other group applied “SGs” without mentioning if they were meshed or not. The accelerated growth of a new epithelium between the meshes that covered the entire empty spaces in a short period of time was really amazing in our patient.
Differences observed between the study of Rasulov’s and our’s
Differences between this study and Rasulov’s  were observed by us: (1) the type of cells used by Rasulov were designated as “allogeneic fibroblast FMSCs” but their phenotype, features of the donor, testing for infectious agents, or other data of these cells were not described in their paper. Our’s were bone marrow MSCs obtained from a unique cadaver donor and fulfilled the phenotyping criteria for MSCs as well as all other requirements by local law to be transplantable including all the tests done to detect possible adventitious agents. No microchimerism was observed after several determinations done at different moments of the patient’s follow-up and no immune adverse events were seen at any time. (2) The Russian group did not specify by which way they applied the cells on the surface of the patient’s wounds. We sprayed the CMSCs into a blood cryoprecipitate that polymerized in situ. (3) Our cell culture method did not involve the use of bovine fetal serum but HPL. It was obtained from platelet-rich plasma having an outstanding potential to promote the growth of CMSCs while maintaining their phenotype and differentiation capacities. (4) We have also always used a transparent polymeric film to cover the wounds after the cell treatments. Rasulov’s group employed just gauze. It is interesting to say that every time stem cells with fibrin were used, a yellowish creamy material under the film was always observed with its characteristic appearance but without wound infection. This could be a promoting interesting material for the healing processes of the wounds that surely deserve further studies and maybe also the essence for a future kind of regenerative product. (5) The development of the granulation-like tissue and its “hyper-proliferation” was rapidly observed in all areas treated with CMSCs both by us (as we also did in our previous pig burned model) and Rasulov’s group.
The granulation-like tissue
As far as we know, this is probably a very early vascularized “neo-dermal-like matrix” under an active growth and differentiation natural program, and not just simply a “granulation tissue”. This new matrix behaves as a novel and may be also as a “universal” scaffold allowing very well for AMSG attachment and may be later appearance of keratinocytes and the production of a mature epidermis. In this way, keratinocytes could come at an early time from the edges of the wounds or may be by direct differentiation from resident MSCs later on after neo-matrix organization .
The first experience using CMSCs in the treatment of a burned patient
In any case, our future challenge in relation to the regeneration processes and in order to obtain a faster healing of severe deep burns as well as many other lesions or diseases of the body will surely be, as it was considered in our previous editorial to Burns , a more precise management and understanding of the variable of time. In this way, the needed length of time to completely regenerate a full-thickness wound by the simple application of CMSCs could be too long for this type of patients, even for the potential growth and differentiation capacities of these cells. In this scenario, we waited 35 days to apply the AMSGs, while Rasulov’s group did it as soon as 4 days after the cells were delivered on the wounds. Probably, it does not really mean that MSCs do not have the potential to regenerate a complete skin including the epidermis, only that maybe, more time could be needed as they have in this kind of deep burns a long harder complicated work to do by first rebuilding the vasculature and the matrix of a neo-dermis before they could take care of the final regeneration process for the development of a neo-epidermis. By now, these preliminary results are very promising by themselves. If time finally ends to be the critical point, we might have several new major options to be employed besides waiting for whole recovery by the simple action of the cells: (1) To early apply the AMSGs as soon as the granulation-like tissue induced by MSCs is seen as Rasulov did. (2) To put together the MSCs and the AMSGs or one specially made with “very wide meshes”, expecting that the growth promotion advantages given by MSCs would be stimuli which is enough to rapidly regenerate the whole skin in a shorter period of time while needing and using much less residual healthy skin from the patients for the auto-grafting. (3) To early use cultured keratinocytes/epidermal grafts or just keratinocyte stem cells with MSCs. (4) To deliver MSCs in novel different ways like in the shape of “spheroids” as we have previously described . This could accelerate the time to complete regeneration specially if keratinocytes could also be grown in the outer surface of these spheroids. (5) To potentially use “intelligent matrices” with nanoparticles and stem cells to accelerate the time for healing . It is important to say that the patient did not have any adverse effect at any time even after more than 3 years of follow-up. He always showed a very well tolerance to the treatment with CMSCs. At this moment, we see almost no scar or deformity in the places treated with CMSCs. The patient looks and feels clinically very good. There are no functional sequelae, and he re-started to work very soon after being discharged from the hospital.
This is mainly a descriptive as well as an observational study of all the chronological events seen in this only one and “first patient” treated in the world with CMSCs. Our preliminary experience and our early results show an outstanding safety data in the use of CMSCs in our first severe burned patient treated in this way. Based on all this, we think that improvements in the use of CMSCs for burns might be possible in the near future, and a lot of time as well as many lives could be saved by many other research teams all over the world.
Our special thanks to Dr. Jorge Arrúa, former Director of the Burns and Plastic Surgery Department, San Martín Hospital, Province of Buenos Aires Ministry of Health, Argentina, for his contributions and inspiration for the advancement of burns treatment. Also, we acknowledge the CUCAIBA and the Province of Buenos Aires Ministry of Health, Argentina, for funding this Research Project.
Source of funding
All the research was supported by CUCAIBA, Ministry of Health, Province of Buenos Aires, Argentina.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- M. F. Rasulov, A. V. Vasil’chenkov, N. A. Onishchenko, M. E. Krasheninnikov, V. I. Kravchenko, T. L. Gorshenin,R. E. Pidtsan, and I. V. Potapo. First experience in the use of bone marrow mesenchymal stem cells for the treatment of a patient with deep skin burns. Bull Exp Biol Med. 2005;139(1):141-4.Google Scholar
- Mansilla E, Marin GH, Sturla F, Drago HE, Gil MA, Salas E, et al. Human mesenchymal stem cells are tolerized by mice and improve skin and spinal cord injuries. Transplant Proc. 2005;37(1):292–4.View ArticlePubMedGoogle Scholar
- Mansilla E, Marín GH, Drago H, Sturla F, Salas E, Gardiner C, et al. Bloodstream cells phenotypically identical to human mesenchymal bone marrow stem cells circulate in large amounts under the influence of acute large skin damage: new evidence for their use in regenerative medicine. Transplant Proc. 2006;38(3):967–9.View ArticlePubMedGoogle Scholar
- Mansilla E, Spretz R, Larsen G, Nuñez L, Drago H, Sturla F, et al. Outstanding survival and regeneration process by the use of intelligent acellular dermal matrices and mesenchymal stem cells in a burn pig model. Transplant Proc. 2010;42(10):4275. 8.View ArticlePubMedGoogle Scholar
- Mansilla E, Aquino VD, Roque G, Tau JM, Maceira A. Time and regeneration in burns treatment: heading into the first worldwide clinical trial with cadaveric mesenchymal stem cells. Burns. 2012;38(3):450–2.View ArticlePubMedGoogle Scholar
- Mansilla E, Mártire K, Roque G, Tau JM, Marín GH, Castuma MV, Orlandi G, Tarditti A. salvage of cadaver stem cells (CSCs) as a routine procedure: history or future for regenerative medicine. J Transplant Technol Res. 2013; 3(118). doi:10.4172/2161-0991.1000118.
- Sharma RK, John JR. Role of stem cells in the management of chronic wounds. Indian J Plast Surg. 2012;45(2):237–43. doi:10.4103/0970-0358.101286.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang S, Okun MS, Suslov O, Zheng T, McFarland NR, Vedam-Mai V, et al. Neurogenic potential of progenitor cells isolated from postmortem human Parkinsonian brains. Brain Res. 2012;1464:61–72.View ArticlePubMedPubMed CentralGoogle Scholar
- Klassen H, Ziaeian B, Kirov II, Young MJ, Schwartz PH. Isolation of retinal progenitor cells from post-mortem human tissue and comparison with autologous brain progenitors. J Neurosci Res. 2004;77(3):334–43.View ArticlePubMedGoogle Scholar
- Mugishima H, Terasaki P, Sueyoshi A. Bone marrow from cadaver donors for transplantation. Blood. 1985;65(2):392–6.PubMedGoogle Scholar
- Michalova J, Savvulidi F, Sefc L, Forgacova K, Necas E. Cadaveric bone marrow as potential source of hematopoietic stem cells for transplantation. Chimerism. 2011;2(3):86–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Ray RN, Cassell M, Chaplin Jr H. A new method for the preparation of human cadaver bone marrow for transfusion. Blood. 1961;17:97–108.PubMedGoogle Scholar
- Liu PL, Ogawa M, Crook L, Ochia R, Upshur JK. Proliferative function of cadaveric bone marrow cells. Am J Hematol. 1978;5(2):145–50.View ArticlePubMedGoogle Scholar
- Rao AS, Fontes P, Zeevi A, Trucco M, Shapiro R, Demetris AJ, et al. Combined bone marrow and whole organ transplantation from the same donor. Transplant Proc. 1994;26(6):3377–8.PubMedPubMed CentralGoogle Scholar
- Mansilla E, Díaz Aquino V, Roque G, Tau JM, Maceira A, Ichim T. Building small spheroids/regenerative units for hair loss treatment: just imitating nature in an industrialized manner. Hair : Therap Transplantat. 2011;1:1.Google Scholar