Immunological response after SARS-CoV-2 infection and mRNA vaccines in patients with myasthenia gravis treated with Rituximab.

Immunological response after SARS-CoV-2 infection and mRNA vaccines in patients with myasthenia gravis treated with Rituximab.
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DOI:
10.1016/j.nmd.2023.02.005
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发表时间:
2023-03
影响因子:
2.8
通讯作者:
Evoli, Amelia
Evoli, Amelia
中科院分区:
医学4区
文献类型:
--
作者:
Damato, Valentina;Spagni, Gregorio;Monte, Gabriele;Scandiffio, Letizia;Cavalcante, Paola;Zampetti, Nicole;Fossati, Marco;Falso, Silvia;Mantegazza, Renato;Battaglia, Alessandra;Fattorossi, Andrea;Evoli, Amelia

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In this study we employed a comprehensive immune profiling approach to determine innate and adaptive immune response to SARS-CoV-2 infection and mRNA vaccines in patients with myasthenia gravis receiving rituximab. By multicolour cytometry, dendritic and natural killer cells, B- and T-cell subsets, including T-cells producing IFN-γ stimulated with SARS-CoV-2 peptides, were analysed after infection and mRNA vaccination. In the same conditions, anti-spike antibodies and cytokines’ levels were measured in sera. Despite the impaired B cell and humoral response, rituximab patients showed an intact innate, CD8 T-cell and IFN-γ specific CD4+ and CD8+ T-cell response after infection and vaccination, comparable to controls. No signs of cytokine mediated inflammatory cascade was observed. Our study provides evidence of protective immune response after SARS-CoV-2 infection and mRNA vaccines in patients with myasthenia gravis on B cell depleting therapy and highlights the need for prospective studies with larger cohorts to clarify the role of B cells in SARS-CoV-2 immune response.
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