2026-07-21T14:05:57Zhttps://repisalud.isciii.es/rest/oai/request
oai:repisalud.isciii.es:20.500.12105/66942024-09-27T08:34:23Zcom_20.500.12105_19604com_20.500.12105_2051col_20.500.12105_19605
Repisalud author Alvino, Valeria Vincenza author Fernandez-Jimenez, Rodrigo author Rodriguez-Arabaolaza, Iker author Slater, Sadie author Mangialardi, Giuseppe author Avolio, Elisa author Spencer, Helen author Culliford, Lucy author Hassan, Sakinah author Sueiro Ballesteros, Lorena author Herman, Andrew author Ayaon-Albarran, Ali author Galan-Arriola, Carlos author Sanchez-Gonzalez, Javier author Hennessey, Helena author Delmege, Catherine author Ascione, Raimondo author Emanueli, Costanza author Angelini, Gianni author Ibáñez, Borja author Madeddu, Paolo funder British Heart Foundation funder Medical Research Council (Reino Unido) funder National Health Service (Reino Unido) funder Ministerio de Economía, Industria y Competitividad (España) funder Fundación Jesús Serra funder Fundación Interhospitalaria de Investigación Cardiovascular funder Centro Nacional de Investigaciones Cardiovasculares Carlos III (España) funder Instituto de Salud Carlos III funder Fundación ProCNIC 2018-11-22T08:10:54Z 2018-11-22T08:10:54Z 2018 J Am Heart Assoc. 2018; 7(2):e006727 10.1161/JAHA.117.006727 2047-9980 Journal of the American Heart Association 29358198 http://hdl.handle.net/20.500.12105/6694 Background-Transplantation of adventitial pericytes (APCs) promotes cardiac repair in murine models of myocardial infarction. The aim of present study was to confirm the benefit of APC therapy in a large animal model. Methods and Results-We performed a blind, randomized, placebo-controlled APC therapy trial in a swine model of reperfused myocardial infarction. A first study used human APCs (hAPCs) from patients undergoing coronary artery bypass graft surgery. A second study used allogeneic swine APCs (sAPCs). Primary end points were (1) ejection fraction as assessed by cardiac magnetic resonance imaging and (2) myocardial vascularization and fibrosis as determined by immunohistochemistry. Transplantation of hAPCs reduced fibrosis but failed to improve the other efficacy end points. Incompatibility of the xenogeneic model was suggested by the occurrence of a cytotoxic response following invitro challenge of hAPCs with swine spleen lymphocytes and the failure to retrieve hAPCs in transplanted hearts. We next considered sAPCs as an alternative. Flow cytometry, immunocytochemistry, and functional/cytotoxic assays indicate that sAPCs are a surrogate of hAPCs. Transplantation of allogeneic sAPCs benefited capillary density and fibrosis but did not improve cardiac magnetic resonance imaging indices of contractility. Transplanted cells were detected in the border zone. Conclusions-Immunologic barriers limit the applicability of a xenogeneic swine model to assess hAPC efficacy. On the other hand, we newly show that transplantation of allogeneic sAPCs is feasible, safe, and immunologically acceptable. The approach induces proangiogenic and antifibrotic benefits, though these effects were not enough to result in functional improvements. eng Angiogenesis Cell therapy Large animal models Myocardial infarction Pericytes Transplantation of Allogeneic Pericytes Improves Myocardial Vascularization and Reduces Interstitial Fibrosis in a Swine Model of Reperfused Acute Myocardial Infarction journal article URL https://repisalud.isciii.es/bitstreams/bb5b58e5-8d18-4ec6-8ad0-d18f82b3bea6/download File MD5 50d83e9fefd83aa6e5f035602213ccb1 6263169 application/pdf TransplantationAllogeneicPericytesImproves_2018.pdf URL https://repisalud.isciii.es/bitstreams/d7ba0d14-9f48-4eb6-8bd4-146745d3063b/download File MD5 f913c395ed7c68e8f10116e6232251b3 456670 application/pdf TransplantationAllogeneicPericytesImproves_2018-sup-0001-supinfo.pdf URL https://repisalud.isciii.es/bitstreams/194cc73d-4728-4423-8d7b-354a5549a798/download File MD5 ec830641a99a9d35b4ea0a8ea08432c7 131932 text/plain TransplantationAllogeneicPericytesImproves_2018.pdf.txt URL https://repisalud.isciii.es/bitstreams/ccb6c988-18e3-43e9-8d20-d422ad79adb0/download File MD5 c6546c712fd6e5fffd4090f35913d5ee 30555 text/plain TransplantationAllogeneicPericytesImproves_2018-sup-0001-supinfo.pdf.txt