Terapias avanzadas en enfermedades raras

Autores/as

  • Cristina Fillat Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) - Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) https://orcid.org/0000-0002-0801-3338
  • Marcela del Río Universidad Carlos III de Madrid - Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) - Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) - Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD) https://orcid.org/0000-0003-2910-7189
  • Lucía Martínez-Santamaría Universidad Carlos III de Madrid - Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) - Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) - Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD) https://orcid.org/0000-0002-9637-2364
  • Juan A. Bueren Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) - Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) - Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD) https://orcid.org/0000-0002-3228-7013

DOI:

https://doi.org/10.3989/arbor.2018.789n3009

Palabras clave:

Terapia génica, terapia celular, ingeniería de tejidos, enfermedades raras

Resumen


Las terapias avanzadas comprenden un grupo de medicamentos biológicos basados en la terapia génica, la terapia celular y la ingeniería de tejidos. En este artículo se presentan algunos conceptos básicos, se describen las estrategias más prometedoras y se detallan los resultados de diferentes ensayos clínicos para un grupo significativo de enfermedades, especialmente las enfermedades hereditarias monogénicas. Se hace un mayor hincapié en la terapia génica ex vivo en enfermedades del sistema hematopoyético, al ser el grupo de enfermedades pioneras que además han orientado la investigación en el campo. Destacamos también algunos ejemplos de éxito de terapia génica in vivo y señalamos la contribución de la terapia celular y de la ingeniería de tejidos al grupo de enfermedades raras de la piel. Pretendemos con ello dar una visión de la situación de las terapias avanzadas en enfermedades raras y señalamos algunas de las vías de futuro orientadas al desarrollo de tratamientos más eficaces y seguros.

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Citas

Adair, J. E., Sevilla, J., Díaz de Heredia, C., Becker, P. S., Kiem, H-P. y Bueren, J. A. (2016). Lessons Learned from Two Decades of Clinical Trial Experience in Gene Therapy for Fanconi Anemia. Current Gene Therapy, 16 (5), pp. 338-348. https://doi.org/10.2174/1566523217666170119113029 PMid:28103787

Aiuti, A., Biasco, L., Scaramuzza, S., Ferrua, F., Cicalese, M. P., Baricordi […] y Naldini, L. (2013). Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome. Science, 341 (6148), 1233151. https://doi.org/10.1126/science.1233151

Aiuti, A. y Roncarolo, M. G. (2009). Ten years of gene therapy for primary immune deficiencies. Hematology. American Society of Hematology Education Program Book, 2009 (1), pp. 682-689. https://doi.org/10.1182/asheducation-2009.1.682

Aiuti, A., Roncarolo, M. G. y Naldini, L. (2017). Gene therapy for ADA?SCID, the first marketing approval of an ex vivo gene therapy in Europe: paving the road for the next generation of advanced therapy medicinal products. EMBO Molecular Medicine, 9 (6), e201707573. https://doi.org/10.15252/emmm.201707573 PMid:28396566 PMCid:PMC5452047

Aiuti, A., Slavin, S., Aker, M., Ficara, F., Deola, S., Mortellaro, A. […] y Bordignon, C. (2002). Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning. Science, 296 (5577), pp. 2410-2413. https://doi.org/10.1126/science.1070104

Atala, A. (2007) Engineering tissues, organs and cells. Journal of Tissue Engineering and Regenerative. Medicine, 1(2), pp. 83-96. https://doi.org/10.1002/term.18 PMid:18038397

Bainbridge, J. W., Smith, A. J., Barker, S. S., Robbie, S., Henderson, R., Balaggan, K. […] y Ali, R. R. (2008). Effect of gene therapy on visual function in Leber's congenital amaurosis. The New England Journal of Medicine, 358 (21), pp. 2231-2239. https://doi.org/10.1056/NEJMoa0802268 PMid:18441371

Bajaj, P., Schweller, R. M., Khademhosseini, A., West, J. L. y Bashir, R. (2014). 3D biofabrication strategies for tissue engineering and regenerative medicine. Annual Review of Biomedical Engineering, 16, pp. 247-276. https://doi.org/10.1146/annurev-bioeng-071813-105155 PMid:24905875 PMCid:PMC4131759

Bauer, J. W., Koller, J., Murauer, E. M., Rosa, L. de, Enzo, E., Carulli, S. […] y Luca, M. de (2017). Closure of a large chronic wound through transplantation of gene-corrected epidermal stem cells. The Journal of Investigative Dermatology 137 (3), pp. 778-781. https://doi.org/10.1016/j.jid.2016.10.038 PMid:27840234

Bennett, J., Ashtari, M., Wellman, J., Marshall, K. A., Cyckowski, L. L., Chung, D. C. […] y Maguire, A. M. (2012). AAV2 gene therapy readministration in three adults with congenital blindness. Science Translational Medicine, 4 (120), 120ra15. https://doi.org/10.1126/scitranslmed.3002865 PMid:22323828 PMCid:PMC4169122

Biffi, A., Montini, E., Lorioli, L., Cesani, M., Fumagalli, F., Plati, T. […] y Naldini, L. (2013). Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy. Science, 341 (6148), 1233158. https://doi.org/10.1126/science.1233158

Blaese, R. M., Culver, K. W., Miller, A. D., Carter, C. S., Fleisher, T., Clerici, M., Shearer, G. […] y Anderson, W. F. (1995). T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 years. Science, 270 (5235), pp. 475-480. https://doi.org/10.1126/science.270.5235.475

Bordignon, C., Mavilio, F., Ferrari, G., Servida, P., Ugazio, A. G., Notarangelo, L. D. […] y Gillio, A. P. (1993). Transfer of the ADA gene into bone marrow cells and peripheral blood lymphocytes for the treatment of patients affected by ADA-deficient SCID. Human Gene Therapy, 4 (4), pp. 513-520. https://doi.org/10.1089/hum.1993.4.4-513 PMid:8399494

Boztug, K., Schmidt, M., Schwarzer, A., Banerjee, P. P., Díez, I. A., Dewey, R. A. […] y Klein, C. (2010). Stem-cell gene therapy for the Wiskott-Aldrich syndrome. The New England Journal of Medicine, 363 (20), pp. 1918- 1927. https://doi.org/10.1056/NEJMoa1003548 PMid:21067383 PMCid:PMC3064520

Braun, C. J., Boztug, K., Paruzynski, A., Witzel, M., Schwarzer, A., Rothe, M. […] y Klein, C. (2014). Gene therapy for Wiskott-Aldrich syndrome--long-term efficacy and genotoxicity. Science Transational. Medicine, 6 (227), 227ra33. https://doi.org/10.1126/scitranslmed.3007280 PMid:24622513

Cartier, N., Hacein-Bey-Abina, S., Bartholomae, C. C., Veres, G., Schmidt, M., Kutschera, I. […] y Aubourg, P. (2009). Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy. Science, 326 (5954), pp. 818-823. https://doi.org/10.1126/science.1171242

Carulli, S., Contin, R., Rosa, L. de, Pellegrini, G., Luca, M. de (2013). The long and winding road that leads to a cure for epidermolysis bullosa. Regenerative Medicine, 8 (4), pp. 467-481. https://doi.org/10.2217/rme.13.33 PMid:23826700

Cavazzana-Calvo, M., Hacein-Bey, S., Saint Basile, G. de, Gross, F., Yvon, E., Nusbaum, P. […] y Fischer, A. (2000). Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science, 288 (5466), pp. 669- 672. https://doi.org/10.1126/science.288.5466.669

Cavazzana-Calvo, M., Payen, E., Negre, O., Wang, G., Hehir, K., Fusil, F. […] y Leboulch, P. (2010). Transfusion independence and HMGA2 activation after gene therapy of human ?-thalassaemia. Nature, 467 (7313), pp. 318-322. https://doi.org/10.1038/nature09328 PMid:20844535 PMCid:PMC3355472

Conget, P., Rodríguez, F., Kramer, S., Allers, C., Simon, V., Palisson, F. […] y Yubero, M. J. (2010). Replenishment of type VII collagen and re-epithelialization of chronically ulcerated skin after intradermal administration of allogeneic mesenchymal stromal cells in two patients with recessive dystrophic epidermolysis bullosa. Cytotherapy, 12 (3), 429-431. https://doi.org/10.3109/14653241003587637 PMid:20230217

Di, W. L., Larcher, F., Semenova, E., Talbot, G. E., Harper, J. I., Río, M. del […] y Qasim, W. (2011). Ex-vivo gene therapy restores LEKTI activity and corrects the architecture of Netherton syndrome-derived skin grafts. Molecular Therapy, 19 (2), pp. 408-416. https://doi.org/10.1038/mt.2010.201 PMid:20877344 PMCid:PMC3034839

Ehrenreich, M. y Ruszczak, Z. (2006). Update on tissue-engineered biological dressings. Tissue Engineering, 12 (9), pp. 2407-2424. https://doi.org/10.1089/ten.2006.12.2407 PMid:16995775

El-Darouti, M., Fawzy, M., Amin, I., Abdel Hay, R., Hegazy, R., Gabr, H. y El-Maadawi, Z. (2016). Treatment of dystrophic epidermolysis bullosa with bone marrow non-hematopoeitic stem cells: a randomized controlled trial. Dermatologic Therapy, 29 (2), pp. 96-100. https://doi.org/10.1111/dth.12305 PMid:26439431

Escámez, M. J., Martínez-Santamaría, L., García, M., Guerrero-Aspizua, S., Carretero, M., Larcher, F., Meana, A., Río, M. del (2011). Bioengineered Skin. En Khopkar, U. (ed.). Skin Biopsy. Perspectives. InTech, pp. 261-296.

Fillat, C. y Altafaj, X. (2012). Gene Therapy for Down Syndrome. Progress in Brain Research, 197, pp. 237-247. https://doi.org/10.1016/B978-0-444-54299-1.00012-1 PMid:22541296

Gache, Y., Baldeschi, C., Río, M. del, Gagnoux-Palacios, L., Larcher, F., Lacour, J. P. y Meneguzzi, G. (2004). Construction of skin equivalents for gene therapy of recessive dystrophic epidermolysis bullosa. Human Gene Therapy, 15 (10), pp. 921-933. https://doi.org/10.1089/hum.2004.15.921 PMid:15585108

García-Gómez, M., Calabria, A., García- Bravo, M., Benedicenti, F., Kosinski, P., López-Manzaneda, S. […] y Segovia, J. C. (2016). Safe and Efficient Gene Therapy for Pyruvate Kinase Deficiency. Molecular Therapy, 24 (7), pp. 1187-1198. https://doi.org/10.1038/mt.2016.87 PMid:27138040 PMCid:PMC5088764

Gaspar, H. B., Parsley, K. L., Howe, S., King, D., Gilmour, K. C., Sinclair, J. […] y Thrasher, A. J. (2004). Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector. The Lancet, 364 (9452), pp. 2181-2187. https://doi.org/10.1016/S0140-6736(04)17590-9

Georgiadis, C., Syed, F., Petrova, A., Abdul-Wahab, A., Lwin, S. M., Farzaneh, F. […] y Qasim, W. (2016). Lentiviral engineered fibroblasts expressing codon-optimized COL7A1 restore anchoring fibrils in RDEB. Journal of Investigative Dermatology, 136 (1), pp. 284-292. https://doi.org/10.1038/JID.2015.364 PMCid:PMC4759620

González-Murillo, A., Lozano, M. L., Álvarez, L., Jacome, A., Almarza, E., Navarro, S. […] y Río, P. (2010). Development of lentiviral vectors with optimized transcriptional activity for the gene therapy of patients with Fanconi anemia. Human Gene Therapy, 21(5), pp. 623-630. https://doi.org/10.1089/hum.2009.141 PMid:20001454

Guo, Z., Higgins, C. A., Gillette, B. M., Itoh, M., Umegaki, N., Gledhill, K. […] y Christiano, A. M. (2013). Building a microphysiological skin model from induced pluripotent stem cells. Stem Cell Research Therapy, 4 (1), S2. https://doi.org/10.1186/scrt363 PMid:24564920 PMCid:PMC4029476

Hacein-Bey-Abina, S., Deist, F. Le, Carlier, F., Bouneaud, C., Hue, C., Villartay, J. P. de […] y Cavazzana-Calvo, M. (2002). Sustained correction of X-Linked severe combined immunodeficiency by ex vivo gene therapy. The New England Journal of Medicine, 346 (16), pp. 1185-1193. https://doi.org/10.1056/NEJMoa012616 PMid:11961146

Hacein-Bey-Abina, S., Pai, S. Y., Gaspar, H. B., Armant, M., Berry, C. C., Blanche, S. […] y Thrasher, A. J. (2014). A modified ?-retrovirus vector for X-linked severe combined immunodeficiency. The New England Journal of Medicine, 371 (15), pp. 1407-1417. https://doi.org/10.1056/NEJMoa1404588 PMid:25295500 PMCid:PMC4274995

Hacein-Bey-Abina, S., Saint Basile, G. de y Cavazzana-Calvo, M. (2003). Gene therapy of X-linked severe combined immunodeficiency. Methods in Molecular Biology, 215, pp. 247-259. PMid:12512304

Haurigot, V., Marcó, S., Ribera, A., García, M., Ruzo, A., Villacampa, P. […] y Bosch, F. (2013). Whole body correction of mucopolysaccharidosis IIIA by intracerebrospinal fluid gene therapy. The Journal of Clinical Investigation, 123 (8), pp. 3254-3271. https://doi.org/10.1172/JCI66778 PMid:23863627 PMCid:PMC3726158

Hauswirth, W. W., Aleman, T. S., Kaushal, S., Cideciyan, A. V., Schwartz, S. B., Wang, L. […] y Jacobson, S. G. (2008). Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial. Human Gene Therapy, 19 (10), pp. 979-990. https://doi.org/10.1089/hum.2008.107 PMid:18774912 PMCid:PMC2940541

Hickerson, R. P., Smith, F. J., Reeves, R. E., Contag, C. H., Leake, D., Leachman, S. A. […] y Kaspar, R. L. (2008). Single-nucleotide-specific siARN targeting in a dominant-negative skin model. Journal of Investigative Dermatology, 128 (3), pp. 594-605. https://doi.org/10.1038/sj.jid.5701060 PMid:17914454

Hovnanian, A., Bodemer, C. y McGrath, J. A. (2014). Phase I/II ex vivo gene therapy clinical trial for recessive dystrophic epidermolysis bullosa using skin equivalent grafts genetically corrected with a COL7A1-encoding SIN retroviral vector (GENEGRAFT). Human Gene Therapy Clinical Development, 25 (2), pp. 65–66. https://doi.org/10.1089/humc.2014.2508 PMid:24933565

Kelly, P. F., Radtke, S., Kalle, C. von, Balcik, B., Bohn, K., Mueller, R. […] y Williams, D. A. (2007). Stem cell collection and gene transfer in Fanconi anemia. Molecular Therapy, 15 (1), pp. 211-219. https://doi.org/10.1038/sj.mt.6300033 PMid:17164793

Kohn, D. B., Hershfield, M. S., Carbonaro, D., Shigeoka, A., Brooks, J., Smogorzewska, E. M. […] y Parkman, R. (1998). T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates. Nature Medicine, 4 (7), pp. 775-780. https://doi.org/10.1038/nm0798-775

Leachman, S. A., Hickerson, R. P., Schwartz, M. E., Bullough, E. E., Hutcherson, S. L., Boucher, K. M. […] y Kaspar, R. L. (2010). First-in-human mutation-targeted siARN phase Ib trial of an inherited skin disorder. Molecular Therapy, 18 (2), pp. 442-446. https://doi.org/10.1038/mt.2009.273 PMid:19935778 PMCid:PMC2839285

Lee, V., Singh, G., Trasatti, J. P., Bjornsson, C., Xu, X., Tran, T. N. […] y Karande, P. (2014). Design and fabrication of human skin by three-dimensional bioprinting. Tissue Engineering. Part C: Methods, 20 (6), pp. 473- 484. https://doi.org/10.1089/ten.tec.2013.0335 PMid:24188635 PMCid:PMC4024844

León-Rico, D., Aldea, M., Sánchez-Baltasar, R., Mesa-Nú-ez, C., Record, J., Burns, S. O. […] y Almarza, A. (2016). Lentiviral vector mediated correction of a mouse model of Leukocyte Adhesion Deficiency Type I. Human Gene Therapy, 27 (9), pp. 668-678. https://doi.org/10.1089/hum.2016.016 PMid:27056660 PMCid:PMC5035374

Lombardo, A. y Naldini, L. (2014). Genome Editing: A tool for research and therapy: Targeted genome editing hits the clinic. Nature Medicine, 20 (10), pp. 1101-1103. https://doi.org/10.1038/nm.3721 PMid:25295939

Llames, S., García, E., García, V., Río, M. del, Larcher, F., Jorcano, J. L. [...] y Meana, A. (2006). Clinical results of an autologous engineered skin. Cell and Tissue Banking, 7 (1), pp. 47-53. https://doi.org/10.1007/s10561-004-7253-4 PMid:16511664

Llames, S. G., Río, M. del, Larcher, F., García, E., García, M., Escámez, M. J. […] y Meana, A. (2004). Human plasma as a dermal scaffold for the generation of a completely autologous bioengineered skin. Transplantation, 77 (3), pp. 350-355. https://doi.org/10.1097/01.TP.0000112381.80964.85 PMid:14966407

Maguire, A. M., Simonelli, F., Pierce, E. A., Pugh Jr., E. N, Mingozzi, F., Bennicelli, J. […] y Bennett, J. (2008). Safety and efficacy of gene transfer for Leber's congenital amaurosis. The New England Journal Medicine, 358 (21), pp. 2240-2248. https://doi.org/10.1056/NEJMoa0802315 PMid:18441370 PMCid:PMC2829748

Mavilio, F., Pellegrini, G., Ferrari, S., Nunzio, F. di, Iorio, E. di, Recchia, A. […] y Luca, M. de (2006). Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. Nature Medicine, 12 (12), pp. 1397-1402. https://doi.org/10.1038/nm1504 PMid:17115047

Meza, N. W., Alonso-Ferrero, M. E., Navarro, S., Quintana-Bustamante, O., Valeri, A., García-Gómez, M. […] y Segovia, J. C. (2009). Rescue of pyruvate kinase deficiency in mice by gene therapy using the human isoenzyme. Molecular Therapy, 17 (12), pp. 2000-2009. https://doi.org/10.1038/mt.2009.200 PMid:19755962 PMCid:PMC2814388

Mingozzi, F. y High, K. A. (2011). Therapeutic in vivo gene transfer for genetic disease using AAV: progress and challenges. Nature Reviews Genetics, 12 (5), pp. 341-355. https://doi.org/10.1038/nrg2988 PMid:21499295

Modlich, U., Navarro, S., Zychlinski, D., Maetzig, T., Knoess, S., Brugman, M. H. […] y Baum, C. (2009). Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectors. Molecular Therapy, 17 (11), pp. 1919-1928. https://doi.org/10.1038/mt.2009.179 PMid:19672245 PMCid:PMC2835038

Ott, M. G., Schmidt, M., Schwarzwaelder, K., Stein, S., Siler, U., Koehl, U. […] y Grez, M. (2006). Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1. Nature Medicine, 12 (4), pp. 401-409. https://doi.org/10.1038/nm1393 PMid:16582916

Petrof, G., Lwin, S. M., Martínez-Queipo, M., Abdul-Wahab, A., Tso, S., Mellerio, J. E. […] y McGrath, J. A. (2015). Potential of systemic allogeneic mesenchymal stromal cell therapy for children with recessive dystrophic epidermolysis bullosa. The Journal of Investigative Dermatology, 135 (9), pp. 2319-2321. https://doi.org/10.1038/jid.2015.158 PMid:25905587 PMCid:PMC5696540

Petrof, G., Martínez-Queipo, M., Mellerio, J. E., Kemp, P. y McGrath, J. A. (2013). Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial. British Journal of Dermatology, 169 (5), pp. 1025-1033. https://doi.org/10.1111/bjd.12599 PMid:24032424

Río, M. del, Larcher, F., Serrano, F., Meana, A., Mu-oz, M., García, M. [...] y Jorcano, J. L. (2002). A preclinical model for the analysis of genetically modified human skin in vivo. Human Gene Therapy, 13 (8), pp. 959-968. https://doi.org/10.1089/10430340252939069 PMid:12031128

Río, P., Navarro, S., Guenechea, G., Sánchez-Domínguez, R., Lamana, M. L., Ya-ez, R. […] y Bueren, J. (2017). Engraftment and in vivo proliferation advantage of gene corrected mobilized CD34+ cells from Fanconi anemia patients. Blood, 130 (13). https://doi.org/10.1182/blood-2017-03-774174 PMid:28801449

Rosa, L. de, Carulli, S., Cocchiarella, F., Quaglino, D., Enzo, E., Franchini, E. […] y Luca, M. de (2013). Long-term stability and safety of transgenic cultured epidermal stem cells in gene therapy of junctional epidermolysis bullosa. Stem Cell Reports, 2 (1), pp. 1-8. https://doi.org/10.1016/j.stemcr.2013.11.001 PMid:24511464 PMCid:PMC3916757

Salido, E., Rodríguez-Pena, M., Santana, A., Beattie, S. G., Petry, H. y Torres, A. (2011). Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer. Molecular Therapy, 19 (5), pp. 870-875. https://doi.org/10.1038/mt.2010.270 PMid:21119625 PMCid:PMC3098628

Schröder, A. R., Shinn, P., Chen, H., Berry, C., Ecker, J. R. y Bushman, F. (2002). HIV-1 integration in the human genome favors active genes and local hotspots. Cell, 110 (4), pp. 521-529. https://doi.org/10.1016/S0092-8674(02)00864-4

Siprashvili, Z., Nguyen, N. T., Gorell, E. S., Loutit, K., Khuu, P., Furukawa, L. K. […] y Marinkovich, M. P. (2016). Safety and wound outcomes following genetically corrected autologous epidermal grafts in patients with recessive dystrophic epidermolysis bullosa. JAMA, 316 (17), pp. 1808-1817. https://doi.org/10.1001/jama.2016.15588 PMid:27802546

Song, J. J. y Ott, H. C. (2011). Organ engineering based on decellularized matrix scaffolds. Trends in Molecular Medicine, 17 (8), pp. 424-432. https://doi.org/10.1016/j.molmed.2011.03.005 PMid:21514224

Stein, S., Ott, M. G., Schultze-Strasser, S., Jauch, A., Burwinkel, B., Kinner, A. […] y Grez, M. (2010). Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease. Nature Medicine, 16 (2), pp. 198- 204. https://doi.org/10.1038/nm.2088 PMid:20098431

Tamai, K., Yamazaki, T., Chino, T., Ishii, M., Otsuru, S., Kikuchi, Y. […] y Kaneda, Y. (2011). PDGFRalpha-positive cells in bone marrow are mobilized by high mobility group box 1 (HMGB1) to regenerate injured epithelia. Proceedings of the National Academy of Sciences USA, 108 (16), pp. 6609- 6614. https://doi.org/10.1073/pnas.1016753108 PMid:21464317 PMCid:PMC3081004

Tolar, J., Becker, P. S., Clapp, D. W., Hanenberg, H., Heredia, C. D. de, Kiem, H. P. […] y Bueren, J. (2012). Gene therapy for Fanconi anemia: one step closer to the clinic. Human Gene Therapy, 23 (2), pp. 141-144. https://doi.org/10.1089/hum.2011.237 PMid:22248350 PMCid:PMC3277737

Tolar, J. y Wagner, J. E. (2013). Allogeneic blood and bone marrow cells for the treatment of severe epidermolysis bullosa: repair of the extracellular matrix. The Lancet, 382 (9899), pp. 1214-1223. https://doi.org/10.1016/S0140-6736(13)61897-8

Torres-Torronteras, J., Viscomi, C., Cabrera-Pérez, R., Cámara, Y., Meo, I. di, Barquinero, J. [...] y Martí, R. (2014). Gene therapy using a liver-targeted AAV vector restores nucleoside and nucleotide homeostasis in a murine model of MNGIE. Molecular Therapy, 22 (5), pp. 901-907. https://doi.org/10.1038/mt.2014.6 PMid:24448160 PMCid:PMC4015233

Venugopal, S. S., Yan, W., Frew, J. W., Cohn, H. I., Rhodes, L. M., Tran, K. […] y Murrell, D. F. (2013). A phase II randomized vehicle-controlled trial of intradermal allogeneic fibroblasts for recessive dystrophic epidermolysis bullosa. Journal of American Academy of Dermatology, 69 (6), pp. 898-908. https://doi.org/10.1016/j.jaad.2013.08.014 PMid:24075228

Wagner, J. E., Ishida-Yamamoto, A., McGrath, J. A., Hordinsky, M., Keene, D. R., Woodley, D. T. […] y Tolar, J. (2010). Bone marrow transplantation for recessive dystrophic epidermolysis bullosa. The New England Journal of Medicine, 363 (7), pp. 629-639. https://doi.org/10.1056/NEJMoa0910501 PMid:20818854 PMCid:PMC2967187

Wong, T., McGrath, J. A. y Navsaria, H. (2007). The role of fibroblasts in tissue engineering and regeneration. British Journal of Dermatology, 156 (6), pp. 1149-1155. https://doi.org/10.1111/j.1365-2133.2007.07914.x PMid:17535219

Publicado

2018-09-30

Cómo citar

Fillat, C., del Río, M., Martínez-Santamaría, L., & Bueren, J. A. (2018). Terapias avanzadas en enfermedades raras. Arbor, 194(789), a467. https://doi.org/10.3989/arbor.2018.789n3009

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