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

被引:5
|
作者
Damato, Valentina [1 ,2 ,7 ]
Spagni, Gregorio [1 ,3 ]
Monte, Gabriele [1 ,4 ]
Scandiffio, Letizia [5 ]
Cavalcante, Paola [5 ]
Zampetti, Nicole [6 ]
Fossati, Marco [6 ]
Falso, Silvia [1 ]
Mantegazza, Renato [5 ]
Battaglia, Alessandra [6 ]
Fattorossi, Andrea [6 ]
Evoli, Amelia [1 ,3 ]
机构
[1] Univ Cattolica Sacro Cuore, Dept Neurosci, Rome, Italy
[2] Univ Florence, Dept Neurosci Drugs & Child Hlth, Florence, Italy
[3] Fdn Policlin Univ A Gemelli, IRCCS, Neurol Inst, Rome, Italy
[4] Bambino Gesu Childrens Hosp IRCCS, Neurosci Dept, Rome, Italy
[5] Fdn IRCCS Ist Neurol Carlo Besta, Neurol Neuroimmunol & Neuromuscular Dis Unit 4, Milan, Italy
[6] Fdn Policlin Univ Agostino Gemelli IRCCS, Dept Women Children & Publ Hlth Sci, Rome, Italy
[7] Univ Florence, Dept Neurosci Drugs & Child Hlth, Viale Pieraccini 6, I-50139 Florence, Italy
关键词
Myasthenia gravis; Rituximab; Sars-CoV2; Vaccination;
D O I
10.1016/j.nmd.2023.02.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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-gamma 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-gamma 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. (c) 2023 Elsevier B.V. All rights reserved.
引用
收藏
页码:288 / 294
页数:7
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