SARS-CoV-2-Specific T Lymphocytes Analysis in mRNA-Vaccinated Patients with B-Cell Lymphoid Malignancies on Active Treatment

Author:

García Ramírez Patricia1ORCID,Callejas Charavia Marta1,Oliva Martin Raquel23,Gómez La Hoz Ana María23,Ortega Miguel Ángel23ORCID,García Suárez Julio1,Álvarez-Mon Melchor23ORCID,Monserrat Sanz Jorge23ORCID

Affiliation:

1. Hematology Department, University Hospital “Príncipe de Asturias”, Alcalá de Henares, 28805 Madrid, Spain

2. Department of Medicine, University of Alcalá, Alcalá de Henares, 28871 Madrid, Spain

3. IRYCIS Unit (Instituto Ramón y Cajal de Investigación Sanitaria), 28034 Madrid, Spain

Abstract

Background: Patients with B-lymphocyte malignancies (BCMs) receiving B-lymphocyte-targeted therapies have increased risk of severe COVID-19 outcomes and impaired antibody response to SARS-CoV-2 mRNA vaccination in comparison to non-hematologic oncologic patients or general population. Consequently, it is vital to explore vaccine-induced T-lymphocyte responses in patients referred for the understanding of immune protection against SARS-CoV2 infections. The objective of the present study was to analyze the recall immune responses carried out by T lymphocytes after two COVID-19 mRNA vaccine doses. Methods: We enrolled 40 patients with BCMs and 10 healthy controls (HCs) after 4 weeks from the second mRNA vaccine dose. Spike (S)-specific T-lymphocyte responses were assessed in peripheral blood mononuclear lymphocytes (PBMCs) by intracellular IFN-γ staining combined with flow cytometry. Furthermore, the humoral response was assessed with the measurement of anti-spike antibodies. Results: From March to July 2021, 40 patients (median age 68) received mRNA vaccines. The overall antibody response for BCMs was 52.5% versus 100% for the healthy controls (p = 0.008). The antibody response was different across BCMs: 18.75% for non-Hodgkin lymphoma, 54.5% for chronic lymphocytic leukemia, and 92.3% for multiple myeloma. Responses varied by malignancy type and treatment, with anti-CD20 therapies showing the lowest response (6.7%). T-lymphocyte analysis revealed reduced numbers and altered differentiation stages in patients compared to the controls. However, the vaccine-induced T response was generally robust, with variations in specific T subpopulations. Conclusions: mRNA vaccines induced significant humoral and cellular immune responses in B-cell lymphoid malignancy patients, although responses varied by treatment type and malignancy. Further research is needed to optimize vaccination strategies in this population.

Funder

Fundación para la Investigación Biomédica del Hospital Universitario Príncipe de Asturias

Publisher

MDPI AG

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