Gustavo Horacio Marín
National University of La Plata
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Publication
Featured researches published by Gustavo Horacio Marín.
Journal of Translational Medicine | 2009
Zhaohui Zhong; Amit N. Patel; Thomas E. Ichim; Neil H. Riordan; Hao Wang; Wei Ping Min; Erik J Woods; Michael A. Reid; Eduardo Mansilla; Gustavo Horacio Marín; Hugo Drago; Michael P. Murphy; Boris Minev
Endometrial Regenerative Cells (ERC) are a population of mesenchymal-like stem cells having pluripotent differentiation activity and ability to induce neoangiogenesis. In vitro and animal studies suggest ERC are immune privileged and in certain situations actively suppress ongoing immune responses. In this paper we describe the production of clinical grade ERC and initial safety experiences in 4 patients with multiple sclerosis treated intravenously and intrathecally. The case with the longest follow up, of more than one year, revealed no immunological reactions or treatment associated adverse effects. These preliminary data suggest feasibility of clinical ERC administration and support further studies with this novel stem cell type.
PLOS ONE | 2013
Nelly Mezzaroba; Sonia Zorzet; Erika Secco; Stefania Biffi; Claudio Tripodo; Marco Calvaruso; Ramiro Mendoza-Maldonado; Sara Capolla; Marilena Granzotto; Ruben Spretz; Gustavo Larsen; Sandra Noriega; Marianna Lucafò; Eduardo Mansilla; Chiara Garrovo; Gustavo Horacio Marín; Gabriele Baj; Valter Gattei; Gabriele Pozzato; Luis Nuñez; Paolo Macor
Current B-cell disorder treatments take advantage of dose-intensive chemotherapy regimens and immunotherapy via use of monoclonal antibodies. Unfortunately, they may lead to insufficient tumor distribution of therapeutic agents, and often cause adverse effects on patients. In this contribution, we propose a novel therapeutic approach in which relatively high doses of Hydroxychloroquine and Chlorambucil were loaded into biodegradable nanoparticles coated with an anti-CD20 antibody. We demonstrate their ability to effectively target and internalize in tumor B-cells. Moreover, these nanoparticles were able to kill not only p53 mutated/deleted lymphoma cell lines expressing a low amount of CD20, but also circulating primary cells purified from chronic lymphocitic leukemia patients. Their safety was demonstrated in healthy mice, and their therapeutic effects in a new model of Burkitts lymphoma. The latter serves as a prototype of an aggressive lympho-proliferative disease. In vitro and in vivo data showed the ability of anti-CD20 nanoparticles loaded with Hydroxychloroquine and Chlorambucil to increase tumor cell killing in comparison to free cytotoxic agents or Rituximab. These results shed light on the potential of anti-CD20 nanoparticles carrying Hydroxychloroquine and Chlorambucil for controlling a disseminated model of aggressive lymphoma, and lend credence to the idea of adopting this therapeutic approach for the treatment of B-cell disorders.
Transplantation Proceedings | 2010
Hugo Drago; Gustavo Horacio Marín; Flavio Sturla; Gustavo Roque; Mártire K; V. Díaz Aquino; R. Lamonega; C. Gardiner; Thomas E. Ichim; Neil H. Riordan; J.C. Raimondi; S. Bossi; Ali Samadikuchaksaraei; M. van Leeuwen; José María Tau; L. Núñez; Gustavo Larsen; Ruben Spretz; Eduardo Mansilla
We describe a novel technology based on nanoengineered multifunctional acellular biologic scaffolds combined with wound dressings and films of the same kind. This method allows selective delivery and release of shielded biomaterials and bioactive substances to a desired wound or damaged tissue while stimulating the selective anchoring and adhesion of endogenous circulating repairing cells, such as mesenchymal stem cells, to obtain a faster and more physiologic healing process. We also present a new controlled enzymatic debridement process for more effective burned tissue scarolysis. In light of our preliminary in vitro and in vivo data, we are convinced that these approaches can include the use of other kinds of adult stem cells, such as endometrial regenerative cells, to improve the vascularization of the constructs, with great potential in the entire tissue and organ regeneration field but especially for the treatment of severely burned patients, changing the way these lesions may be treated in the future.
Stem Cells International | 2011
Eduardo Mansilla; Vanina Díaz Aquino; Daniel Zambón; Gustavo Horacio Marín; Mártire K; Gustavo Roque; Thomas E. Ichim; Neil H. Riordan; Amit N. Patel; Flavio Sturla; Gustavo Larsen; Ruben Spretz; Luis Nuñez; Carlos Soratti; Ricardo Ibar; Michiel van Leeuwen; José María Tau; Hugo Drago; Alberto Maceira
One of the most important and complex diseases of modern society is metabolic syndrome. This syndrome has not been completely understood, and therefore an effective treatment is not available yet. We propose a possible stem cell mechanism involved in the development of metabolic syndrome. This way of thinking lets us consider also other significant pathologies that could have similar etiopathogenic pathways, like lipodystrophic syndromes, progeria, and aging. All these clinical situations could be the consequence of a progressive and persistent stem cell exhaustion syndrome (SCES). The main outcome of this SCES would be an irreversible loss of the effective regenerative mesenchymal stem cells (MSCs) pools. In this way, the normal repairing capacities of the organism could become inefficient. Our point of view could open the possibility for a new strategy of treatment in metabolic syndrome, lipodystrophic syndromes, progeria, and even aging: stem cell therapies.
Transplantation Proceedings | 2010
Eduardo Mansilla; Ruben Spretz; Gustavo Larsen; Luis Nuñez; Hugo Drago; Flavio Sturla; Gustavo Horacio Marín; Gustavo Roque; Mártire K; V. Díaz Aquino; S. Bossi; C. Gardiner; R. Lamonega; N. Lauzada; J. Cordone; J.C. Raimondi; José María Tau; N.R. Biasi; J.E. Marini; Amit N. Patel; Thomas E. Ichim; Neil H. Riordan; Alberto Maceira
A pig model with a deep large burn was used to study the regeneration process induced by mesenchymal stem cells (MSCs) and acellular pig dermal matrices, made intelligent by the combination with biodegradable nanofibers loaded with growth factors (granulocyte-macrophage colony-stimulating factor and epidermal growth factor) and coated with the anti-CD44 monoclonal antibody (intelligent acellular dermal matrices, IADMs). These IADMs are specially designed to integrate in the wound bed as new biological scaffolds as well as to specifically recruit and attach circulating and/or externally applied MSCs through the anti-CD44 antibody while delivering precise amounts of growth factors. In this way, the reparative process as well as the aesthetic and functional results were enhanced in our burn model. The animal survived, the wound was completely closed, and total regeneration of the skin was obtained without much scarring. Surprisingly, hair follicles and other skin appendages developed despite the severity and deepness of the burn. Even burned muscles and ribs seemed to have undergone a regenerative process by the end of the study. Based on these findings, we have proposed the use of IADMs and autologous, allogeneic or xenogeneic MSCs, as a new paradigm for the future treatment of large burns and probably other dermatological and cosmetic human conditions.
Cancer Biotherapy and Radiopharmaceuticals | 2010
Eduardo Mansilla; Gustavo Horacio Marín; Luis Nuñez; Hugo Drago; Flavio Sturla; Carol J. Mertz; Luis Rivera; Thomas E. Ichim; Neil H. Riordan; Clemente Raimondi
Nonviral delivery systems are relatively easy to produce in the large scale, are safe, and elicit a negligible immune response. Nanoparticles (NPs) offer promise as nonviral vectors as biocompatible and -degradable carriers of drugs with targeting to specific sites by surface receptors of monoclonal antibodies (mAbs). We investigated the effect of four PEG-PLGA (polyethylene glycol-polylactic-co-glycolic acid) NP systems on drug-resistant B-chronic lymphocytic leukemia (B-CLL) cells in vitro, three of them encapsulating the drug, hydroxylchloroquine (HDQ), two with NP surface coatings of mAbs (NP1) CD20, (NP2) CD19, and CD20, and one (NP3) with no mAb, but tagged with the fluorescent marker, fluorescein isothiocyanate. The fourth NP system (NP4) was coated with anti-CD19/FITC and anti-CD20/Alexa-Fluor((R)) antibodies, but did not contain the active drug, HCQ. Our data indicate that PEG-PLGA nanoparticles with surface mAbs are suitable for selective drug delivery to B-CLL cells and produce a strong apoptotic effect when loaded with the lysosomotropic agent, HDQ.
Journal of Cancer Research and Therapeutics | 2010
Gustavo Horacio Marín; Eduardo Mansilla
BACKGROUND B-cell chronic lymphocytic leukemia (B-CLL) still remains as an uncurable disease. Even the newest antineoplastic agents have demonstrated limitations in their efficacy. For this reason, further research of new compounds must be done. New pharmacological properties can be obtained from a great diversity botanical species. Among these products, Magnolia Grandiflora receives our attention since it mainly contains Honokiol which had demonstrated effect against B-CLL cells activating different cell death pathways. AIM To test the ability of Magnolia Grandiflora extracts to induce apoptosis of B-CLL cells in vitro. MATERIALS AND METHODS Herbs extraction: Twenty grams of powdered material were submitted to three consecutives decoctions with 500 ml of distilled water (96 °C), filtered and followed by ultrafiltration with cellulose membrane, lyophilized and reconstituted in AIM-V medium at a final concentration of 10 mg/ml solution. B-CLL chlorambucil-resistant cells were separated and cultivated in the presence of Magnolias extract. Samples of cells were taken from the cultures at 24, 48 and 72 h for apoptosis analysis by flow cytometry measuring positive annexin V (0.1 μg/ml) cells. STATISTICS Apoptosis values were represented by the mean plus or minus SD (± SD) for five independent experiments. Statistical significance was determined by Students t-test. A P value of 0.05 or less was considered as significant. RESULTS AND CONCLUSION This article discusses the apoptosis properties of Magnolia on B-CLL cells. The evidence suggests a potentially effective repertoire for B-CLL treatment. This herb extract might have promising therapy strategies in treating B-CLL or other hematological disease resistant to alkylating agents in clinical practice.
Atencion Primaria | 2008
Gustavo Horacio Marín; Patricia Rivadulla; Laura Negro; Marta Gelemur; Graciela Etchegoyen
Objetivo Establecer la prevalencia de anemia en poblacion adulta y determinar los factores asociados. Diseno Estudio poblacional de corte transversal, con etapa descriptiva y analitica. Emplazamiento Estudio realizado en La Plata, Argentina. Participantes Muestra aleatoria, con estratificacion trietapica considerando area geografica, aspectos sanitarios y nivel socioeconomico de adultos mayores de 18 anos. Resultados y mediciones principales Encuestas socioeconomica y nutricional, estudios hematologico y serico. A quienes se detecto anemia, se les aseguro un tratamiento completo o estudios ulteriores hasta el diagnostico de certeza. Se valoro: peso y talla, hemoglobina, hematies, hematocrito, ferremia, transferrina, ferritina, ingesta diaria de calorias, hidratos de carbono, lipidos, proteinas, calcio, hierro y vitamina C. Se analizo a 1.136 pacientes de los 1.200 seleccionados. La prevalencia de anemia en adultos fue del 26,3%. Numerosas variables, como nivel socioeconomico, aspectos nutricionales o frecuencia de consulta medica, se asocian al riesgo de anemia. Sin embargo, las necesidades basicas insatisfechas —variable compuesta por vivienda precaria y bajo nivel de instruccion—, sexo femenino y residencia en suburbios mantienen la significacion en el analisis multivariable (odds ratio > 2,5). Conclusiones Una de cada 4 personas adultas presenta anemia, y la ferropenia es la causa mas importante. El diagnostico de anemia se asocio, predominantemente, a aspectos sociales, el sexo o el area geografica de residencia. Dicha informacion, utilizada por el Estado para planificar las medidas preventivas, oportunas y focalizadas, podra lograr beneficios no solo en los adultos, sino en toda la comunidad que depende economicamente de ellos.
Current Clinical Pharmacology | 2010
Gustavo Horacio Marín; Eduardo Mansilla; Nelly Mezzaroba; Sonia Zorzet; Luis Nuñez; Gustavo Larsen; Jose M. Tau; Alberto Maceira; Ruben Spretz; Carol J. Mertz; Sabrina Ingrao; Claudio Tripodo; Francesco Tedesco; Paolo Macor
The aim of this study was to determine if Rituximab coated Biodegradable Nanoparticles (BNPs) loaded with Chlorambucil and Hydroxychloroquine could induce apoptosis of B-Chronic Lymphocytic Leukemia (B-CLL), MEC-1 and BJAB cells in vitro and evaluate their toxic and therapeutic effects on a Human/Mouse Model of Burkitt Lymphoma at an exploratory, proof of concept scale. We found that Rituximab-Chlorambucil-Hydroxychloroquine BNPs induce a decrease in cell viability of malignant B cells in a dose-dependent manner. The mediated cytotoxicity resulted from apoptosis, and was confirmed by monitoring the B-CLL cells after Annexin V/propidium iodide staining. Additional data revealed that these BNPs were non toxic for healthy animals, and had prolonged survival in this mice model of human lymphoma.
Gaceta Sanitaria | 2009
Gustavo Horacio Marín; Cecilia Homar; Germán Niedfeld; Graciela Matcovick; Mario Mamonde
OBJECTIVE This paper evaluates the effectiveness of a Public Health program for the elderly based on health promotion and pathologies prevention, in order to avoid complications associated with illnesses and improves the quality of life (QOL) in elderly adults (EA). METHODS A 12 month intervention studies used 700 EA randomized in 2 groups: intervention and control. Each group was submitted to pre-post intervention measurements that included weight, height, blood pressure (BP), cholesterol, lipids, glycaemia, cardiovascular (infarct, stroke) and bone fractures events, hospitalization, and a QOL survey. Intervention consisted of periodic physical activity to fortify muscular groups, as well as recreational activities, nutritional and food manipulation training visits. A medical student was assigned to each participant from the intervention group to assure periodical contact and to share activities. The control group continued with their normal activities during observational period. RESULTS The intervention group showed a significant reduction in the BP, lipids and cholesterol values compared to control group. Reduction on cardiovascular events (-31%), hip fractures (-18.2%) and number of hospital admittance (-21.1%) were obtained for group A in relation to B. The QOL survey showed 28.7% improvement for group A compared with 33.4% improvement compared with control group. CONCLUSION The health program with exhaustive follow-up administration, significantly reduced risk factors and complications associated with aging.