Cellular and humoral immunogenicity of the mRNA-1273 SARS-CoV-2 vaccine in patients with hematologic malignancies

Moraima Jiménez, Elisa Roldán Galvan, Candela Fernandez-Naval, Guillermo Villacampa Javierre, Mónica Martinez-Gallo, Daniel Medina-Gil, Soraya Peralta-Garzón, Gemma Pujadas, Cristina Hernández, Carlota Pagès-Portabella, Mercedes Gironella, Maria Laura Fox, Guillermo Orti, Pere Barba, Tomàs Pumarola Suñé, Alba Cabirta, Eva Catalá, Mercedes Valentín, Ana Marín-Niebla, Alberto OrfaoMarcos González, Magda Campins Martí, Isabel Ruiz-Camps, David Valcárcel, Francesc Xavier Bosch José, Manuel Hernández, Marta Crespo, Juliana Esperalba, Pau Abrisqueta

Producció científica: Contribució a una revistaArticleRecercaAvaluat per experts

45 Cites (Scopus)

Resum

Recent studies have shown a suboptimal humoral response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) messenger RNA (mRNA) vaccines in patients diagnosed with hematologic malignancies; however, data about cellular immunogenicity are scarce. The aim of this study was to evaluate both the humoral and cellular immunogenicity 1 month after the second dose of the mRNA-1273 vaccine. Antibody titers were measured by using the Elecsys and LIAISON anti-SARS-CoV-2 S assays, and T-cell response was assessed by using interferon-γ release immunoassay technology. Overall, 76.3% (184 of 241) of patients developed humoral immunity, and the cellular response rate was 79% (184 of 233). Hypogammaglobulinemia, lymphopenia, active hematologic treatment, and anti-CD20 therapy during the previous 6 months were associated with an inferior humoral response. Conversely, age >65 years, active disease, lymphopenia, and immunosuppressive treatment of graft-versus-host disease (GVHD) were associated with an impaired cellular response. A significant dissociation between the humoral and cellular responses was observed in patients treated with anti-CD20 therapy (the humoral response was 17.5%, whereas the cellular response was 71.1%). In these patients, B-cell aplasia was confirmed while T-cell counts were preserved. In contrast, humoral response was observed in 77.3% of patients undergoing immunosuppressive treatment of GVHD, whereas only 52.4% had a cellular response. The cellular and humoral responses to the SARS-CoV-2 mRNA-1273 vaccine in patients with hematologic malignancies are highly influenced by the presence of treatments such as anti-CD20 therapy and immunosuppressive agents. This observation has implications for the further management of these patients.
Idioma originalEnglish
Pàgines (de-a)774-784
Nombre de pàgines11
RevistaBlood advances
Volum6
DOIs
Estat de la publicacióPublicada - 2021

Fingerprint

Navegar pels temes de recerca de 'Cellular and humoral immunogenicity of the mRNA-1273 SARS-CoV-2 vaccine in patients with hematologic malignancies'. Junts formen un fingerprint únic.

Com citar-ho