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Humoral and Cellular Response to Spike of Delta SARS-CoV-2 Variant in Vaccinated Patients With Multiple Sclerosis.

Authors :
Petrone, Linda
Tortorella, Carla
Aiello, Alessandra
Farroni, Chiara
Ruggieri, Serena
Castilletti, Concetta
Meschi, Silvia
Cuzzi, Gilda
Vanini, Valentina
Palmieri, Fabrizio
Prosperini, Luca
Haggiag, Shalom
Galgani, Simona
Grifoni, Alba
Sette, Alessandro
Gasperini, Claudio
Nicastri, Emanuele
Goletti, Delia
Source :
Frontiers in Neurology; 5/31/2022, Vol. 13, p1-7, 7p
Publication Year :
2022

Abstract

Objectives: We assessed vaccination-induced antibody and cellular response against spike from the ancestral strain and from the Delta Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) variant in patients with Multiple Sclerosis (MS) treated with disease modifying treatments. Methods: We enrolled 47 patients with MS and nine controls ("no MS") having completed the vaccination schedule within 4–6 months from the first dose. The Interferon (IFN)-γ-response to spike peptides derived from the ancestral and the Delta SARS-CoV-2 was measured by enzyme-linked immunoassay (ELISA). Anti-Receptor Binding Domain (RBD) IgG were also evaluated. Results: No significant differences were found comparing the IFN-γ-specific immune response between MS and "no MS" subjects to the ancestral (P = 0.62) or Delta peptide pools (P = 0.68). Nevertheless, a reduced IFN-γ-specific response to the ancestral or to the Delta pools was observed in subjects taking fingolimod or cladribine compared to subjects treated with ocrelizumab or IFN-β. The antibody response was significantly reduced in patients with MS compared to "no MS" subjects (P = 0.0452) mainly in patients taking ocrelizumab or fingolimod. Conclusions: Cellular responses to Delta SARS-CoV-2 variant remain largely intact in patients with MS. However, the magnitude of these responses depends on the specific therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16642295
Volume :
13
Database :
Complementary Index
Journal :
Frontiers in Neurology
Publication Type :
Academic Journal
Accession number :
157190048
Full Text :
https://doi.org/10.3389/fneur.2022.881988