Immune dysfunction prior to and during vaccination in multiple myeloma: a case study based on COVID-19

Autor: Esperanza Martín-Sánchez, Luis-Esteban Tamariz-Amador, Camila Guerrero, Anastasiia Zherniakova, Aintzane Zabaleta, Catarina Maia, Laura Blanco, Diego Alignani, Maria-Antonia Fortuño, Carlos Grande, Andrea Manubens, Jose-Maria Arguiñano, Clara Gomez, Ernesto Perez-Persona, Iñigo Olazabal, Itziar Oiartzabal, Carlos Panizo, Felipe Prosper, Jesus F. San-Miguel, Paula Rodriguez-Otero, Bruno Paiva, the Asociación Vasco-Navarra de Hematología y Hemoterapia (ASOVASNA) cooperative group

Publikováno v: Blood Cancer Journal, Vol 14, Iss 1, Pp 1-9 (2024)

Abstract Infection is the leading cause of death in multiple myeloma (MM). However, the cellular composition associated with immune dysfunction is not defined. We analyzed immune profiles in the peripheral blood of patients with MM (n = 28) and B-cel

Externí odkaz: https://doaj.org/article/d290946f1de348f38a26beba2fae6800

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P1552: AN IMMUNE ATLAS OF THE DYSFUNCTIONAL CELLULAR AND ANTIBODY RESPONSE TO COVID-19 VACCINATION IN HEMATOLOGICAL PATIENTS WITH A MATURE B-CELL NEOPLASM

Autor: Esperanza Martín-Sánchez, Camila Guerrero, Luis-Esteban Tamariz-Amador, Anastasiia Zherniakova, Aintzane Zabaleta, Catarina Maia, Laura Blanco, Maria-Antonia Fortuño, Carlos Grande, Andrea Manubens, Jose-Maria Arguiñano, Clara Gomez Perez, Ernesto Perez Persona, Iñigo Olazabal Eizaguirre, Itziar Oiartzabal, Carlos Panizo, Felipe Prosper, Jesús San Miguel, Paula Rodríguez-Otero, Bruno Paiva

Publikováno v: HemaSphere, Vol 7, p e4536414 (2023)

Externí odkaz: https://doaj.org/article/15c33901c2724df2a83182e9f4979495

Evaluation of the outcomes of newly diagnosed patients with high-risk myelodysplastic syndrome according to the initial therapeutical strategies chosen in usual clinical practice

Autor: Maria Julia, Montoro, Helena, Pomares, Rosa, Coll, Teresa, Bernal Del Castillo, Mar, Tormo, Ana, Jiménez, Salut, Brunet, Javier, Casaño, Itziar, Oiartzabal, María, Díez-Campelo, Fernando, Ramos, Rafael, Romero, Eduardo, Salido-Fiérrez, Carmen, Pedro, Joan, Bargay, Carolina, Muñoz-Novas, Rocío, López, Montserrat, Rafel, David, Valcárcel

Publikováno v: Scientia

Clinical practice; Myelodysplastic syndrome; Treatment Pràctica clínica; Síndrome mielodisplàstica; Tractament Práctica clínica; Síndrome mielodisplásico; Tratamiento Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases witho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c456de335e71f86eacc9140b91ac9eec
https://doi.org/10.1080/10428194.2022.2154604

Myelodysplastic syndromes with 20q deletion: incidence, prognostic value and impact on response to azacitidine of ASXL1 chromosomal deletion and genetic mutations

Autor: Itziar Oiartzabal, Teresa Bernal, Carlos Solano, Eva Villamón, Míriam Gutiérrez, Rosario Abellán, Míriam Vara, María Díez-Campelo, María José Calasanz, Iván Martín, Sara Alvarez, Marisa Calabuig, Aroa Irigoyen, Guillermo Sanz, Isabel Granada, Esperanza Such, Elvira Mora, Rocío García‐Serra, Mª Laura Blanco, Rosa Collado, Rosana Diez, Andres Jerez, Blanca Xicoy, Angela Gil, Mar Tormo

Publikováno v: BRITISH JOURNAL OF HAEMATOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
British Journal of Haematology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol

In myelodysplastic syndromes (MDS), the 20q deletion [del(20q)] may cause deletion of the ASXL1 gene. We studied 153 patients with MDS and del(20q) to assess the incidence, prognostic value and impact on response to azacitidine (AZA) of ASXL1 chromos

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e0e81ebf5e7444eddb0caf6e4af4054
https://doi.org/10.1111/bjh.17675