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Beatriz Rodriguez

Investigadores de los Hospitales Gregorio Marañón y Niño Jesús descubren un tratamiento para un tipo de ictiosis.

Un equipo de investigadores de los hospitales Gregorio Marañón y Niño Jesús ha identificado una alteración en el sistema inmune de una paciente de tan sólo nueve meses con ictiosis, un grupo de enfermedades raras que provocan alteraciones muy graves en la piel y que pueden producir infecciones recurrentes y un retraso del crecimiento en los niños afectados. El descubrimiento, que ha sido publicado en la revista “New England Journal of Medicine”, se ha basado en la identificación de una alteración en el sistema inmune de una niña de 9 meses, lo que ha permitido un tratamiento específico para “bloquear… Leer más »Investigadores de los Hospitales Gregorio Marañón y Niño Jesús descubren un tratamiento para un tipo de ictiosis.

El Marañón participa en un proyecto europeo de inmunoterapia celular frente a la COVID-19.

El proyecto, que cuenta con una inversión de 5 millones de euros, tiene como objetivo comprender mejor el funcionamiento de la respuesta inmunitaria frente al SARS-CoV-2, para desarrollar terapias celulares con linfocitos T que actúen frente a la infección por SARS-CoV-2 y terapias con células T reguladoras (Treg) para neutralizar la hiper-activación inmune responsable del empeoramiento de los pacientes COVID-19. El Laboratorio de Inmuno-regulación, liderado por Rafael Correa Rocha, del Hospital General Universitario Gregorio Marañón participa en un consorcio europeo de hospitales coordinado por el Clínic-IDIBAPS con el apoyo de la empresa Cellnex Telecom que impulsa la investigación sobre inmunoterapias… Leer más »El Marañón participa en un proyecto europeo de inmunoterapia celular frente a la COVID-19.

Platelet and immune characteristics of immune thrombocy-topaenia patients non-responsive to therapy reveal severeimmune dysregulation.

Elena Monzón Manzano, María Teresa Álvarez Román, Raúl Justo Sanz, Hosvan y Fernández Bello, Diana Hernández, Mónica Martín Salces, Larissa Valor, Isabel Rivas Pollmar, Nora V. Butta1 and Víctor Jiménez Yuste. British Society for Haematology and John Wiley & Sons LtdBritish Journal of Haematology, 2020, 189, 943–953 – 16 january 2020. DOI: 10.1111/bjh.16459 Abstract Multifactorial mechanisms leading to diminished platelet counts in immune thrombocytopaenia (ITP) might condition the ability of patients with ITP to respond to treatments. Examining their platelet and immune features, we aimed to detect singular characteristics of patients with ITP who do not respond to any treatment. We… Leer más »Platelet and immune characteristics of immune thrombocy-topaenia patients non-responsive to therapy reveal severeimmune dysregulation.

ABSTRACT: Novel in vivo tracing of the hepatocyte origin of extracellular vesicles in mice with experimental liver disease.

Elena Blázquez-López, Félix Royo, Elena Vázquez-Ogando, Francisco Javier Cubero, Raquel Herrero, Laura Moreno, José A. Lorente, Angel Cogolludo, Rafael Correa, Marjorie Pion, Yulia Nevzorova, Johanna Sierra, Marta Puerto, Ismael Ranz, Agustin Albillos, Jaime Bosch, Rafael Bañares, Jordi Gracia-Sancho, Juan Falcon-Perez, Javier Vaquero. Journal of Hepatology 2020 vol. 73 | S123–S400 DOI:10.1016/S0168-8278(20)30952-1 ABSTRACT: THU 168 Background and Aims: Most information about hepatocytederived exosomes and extracellular vesicles (EVs) and their role in health and disease derives from cell culture experiments, which do not represent the complexity of whole organisms. The lineage reporter mT/mG mouse strain allows the generation of mice that express… Leer más »ABSTRACT: Novel in vivo tracing of the hepatocyte origin of extracellular vesicles in mice with experimental liver disease.

Pigmented Dermatofibrosarcoma Protuberans: Description of a pediatric case.

L M Nieto-Benito, Beatriz Berenguer-Fröhner, Verónica Parra-Blanco, Minia Campos-Domínguez. Rev Chil Pediatr 2020 Feb;91(1):99-104. Epub 2019 Dec 3. DOI: 10.32641/rchped.v91i1.1303.  Abstract Introduction: Bednar tumor is a rare low-grade sarcoma considered the pigmented variant of dermatofibrosarco ma protuberans (DFSP). Objective: To describe the clinical and histopathological characteristics, treatment and evolution of this rare neoplasm. Clinical case: A 9-year old female presented with a 2-year history of an indurated, asymptomatic papule on the back of her fourth left toe. The incisio nal biopsy was compatible with pigmented DFSP. The immunohistochemical study showed intense positivity for CD34 throughout the lesion, with negative factor XIIIa. We complemented the study with molecular… Leer más »Pigmented Dermatofibrosarcoma Protuberans: Description of a pediatric case.

Imbalance in T-Helper 17 Cells and Targeted Therapy in an Infant with SAM-like Syndrome.

Angela Hernández-Martín, Rebeca Kennedy-Batalla, Elvira Cañedo, Esther Bernaldo-de-Quirós, Begoña Carazo-Gallego, Angel Vera, Antonio Torrelo, Lucero Noguera-Morel, Rogelio González-Sarmiento, Marieke Bolling, Marta Martínez-Bonet, Marjorie Pion, Rafael Correa-Rocha. N Engl J Med  2019 Nov 28;381(22):2176-2178. DOI: 10.1056/NEJMc1908531 The SAM syndrome, which is characterized by severe dermatitis, multiple allergies, and metabolic wasting (Online Mendelian Inheritance in Man number, 615508), is a congenital skin disease caused by mutations in the genes encoding either desmoglein-1 (DSG1) or desmoplakin (DSP). These mutations result in reduced epidermal integrity, which may be lethal in children because of recurrent sepsis and extreme undernourishment. The immunopathogenic mechanisms remain uncertain, and no treatments have been available. A 9-month-old girl was referred to our practice… Leer más »Imbalance in T-Helper 17 Cells and Targeted Therapy in an Infant with SAM-like Syndrome.

Analysis of the dysregulation between regulatory B and T cells (Breg and Treg) in human immunodeficiency virus (HIV)-infected patients.

Carolina Gutiérrez, Jacobo Lopez-Abente, Verónica Pérez-Fernández, Adrián Prieto-Sánchez, Rafael Correa-Rocha, Santiago Moreno-Guillen, María-Ángeles Muñoz-Fernández, Marjorie Pion. PLoS One 2019 Mar 27;14(3):e0213744. eCollection 2019. DOI: 10.1371/journal.pone.0213744 Abstract This study examines the relationship between regulatory B (Breg) and T (Treg) compartments, which play crucial roles in the maintenance of immune homeostasis in the context of HIV. Using flow cytometry, the phenotypes of different Breg and Treg subsets from HIV-infected and healthy individuals were analyzed, along with the suppressive capacity of Breg. Peripheral blood samples of thirteen HIV+ treatment-naïve individuals, fourteen treated-HIV+ individuals with undetectable viral load and twelve healthy individuals were analyzed. The absolute counts of Breg and Treg subsets… Leer más »Analysis of the dysregulation between regulatory B and T cells (Breg and Treg) in human immunodeficiency virus (HIV)-infected patients.

Immune dysregulation and Th2 polarization are associated with atopic dermatitis in heart-transplant children: A delicate balance between risk of rejection or atopic symptoms.

Jacobo López-Abente, Esther Bernaldo-de-Quirós, Manuela Camino, Nuria Gil, Esther Panadero, Minia Campos-Domínguez, Elena Seoane-Reula, Juan M Gil-Jaurena, Marjorie Pion, Rafael Correa-Rocha. Am J Transplant 2019 May;19(5):1536-1544. Epub 2019 Jan 25. DOI: 10.1111/ajt.15245 Abstract Atopic dermatitis (AD) has a high incidence in heart-transplant children, and the reason why there is more AD after transplantation is still unknown. We conducted a cross-sectional study comparing 11 AD and 11 non-AD age-matched heart-transplant children, to assess which immune alterations are related to AD in these patients. AD patients had been transplanted at a younger age compared to non-AD, indicating that age at transplant may be determinant in the onset of AD. The earlier thymectomy… Leer más »Immune dysregulation and Th2 polarization are associated with atopic dermatitis in heart-transplant children: A delicate balance between risk of rejection or atopic symptoms.

Human immunodeficiency virus type-1 induces a regulatory B cell-like phenotype in vitro.

Jacobo Lopez-Abente, Adrián Prieto-Sanchez, Maria-Ángeles Muñoz-Fernandez, Rafael Correa-Rocha, Marjorie Pion. Cell Mol Immunol. 2018 Oct;15(10):917-933. Epub 2017 Jul 17.  DOI: 10.1038/cmi.2017.48.  Abstract Individuals infected with human immunodeficiency virus type-1 (HIV-1) usually show a general dysregulation and hyper-activation of the immune system. A direct influence of HIV-1 particles on B-cell phenotypes and functions has been previously described. However, the consequences of B-cell dysregulation are still poorly understood. We evaluated the phenotypic changes in primary B cells after direct contact with HIV-1 particles in comparison with different types of stimuli. The functionality of treated B cells was challenged in co-culture experiments with autologous CD4+ and CD8+ T… Leer más »Human immunodeficiency virus type-1 induces a regulatory B cell-like phenotype in vitro.

CD72/CD100 and PD-1/PD-L1 markers are increased on T and B cells in HIV-1+ viremic individuals, and CD72/CD100 axis is correlated with T-cell exhaustion.

Rafael Correa-Rocha, Jacobo Lopez-Abente, Carolina Gutierrez, Verónica Astrid Pérez-Fernández, Adrián Prieto-Sánchez, Santiago Moreno-Guillen, María-Ángeles Muñoz-Fernández, Marjorie Pion. PLoS One 2018 Aug 30;13(8):e0203419. eCollection 2018. DOI: 10.1371/journal.pone.0203419.  Abstract In our work, we analyzed the role of the CD100/CD72 and PD-1/PD-L1 axes in immune response dysfunction in human immunodeficiency virus (HIV)-1 infection in which high expressions of PD-1 and PD-L1 were associated with an immunosuppressive state via limitation of the HIV-1-specific T-cell responses. CD100 was demonstrated to play a relevant role in immune responses in various pathological processes and may be responsible for immune dysregulation during HIV-1 infection. We investigated the function of CD72/CD100, and PD-1/PDL-1 axes on T… Leer más »CD72/CD100 and PD-1/PD-L1 markers are increased on T and B cells in HIV-1+ viremic individuals, and CD72/CD100 axis is correlated with T-cell exhaustion.