Anti-SARS-CoV-2 T-stem cell memory persists in ocrelizumab-treated MS patients. (October 2022)
- Record Type:
- Journal Article
- Title:
- Anti-SARS-CoV-2 T-stem cell memory persists in ocrelizumab-treated MS patients. (October 2022)
- Main Title:
- Anti-SARS-CoV-2 T-stem cell memory persists in ocrelizumab-treated MS patients
- Authors:
- Guerrera, Gisella
Mandelli, Alessandra
Finardi, Annamaria
Orrico, Mario
D'Orso, Silvia
Picozza, Mario
Noviello, Maddalena
Beretta, Valeria
Bonetti, Bruno
Calabrese, Massimiliano
Marastoni, Damiano
De Rossi, Nicola
Capra, Ruggero
Salvetti, Marco
Buscarinu, Maria Chiara
Inglese, Matilde
Uccelli, Antonio
Moiola, Lucia
Raposo, Catarina
Muros-Le Rouzic, Erwan
Pedotti, Rosetta
Filippi, Massimo
Bonini, Chiara
Battistini, Luca
Borsellino, Giovanna
Furlan, Roberto - Abstract:
- Background: Development of long-lasting anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) T-cell responses in persons with multiple sclerosis (pwMS) treated with ocrelizumab is questioned. Objective: Investigate antiviral T-cell responses after infection with SARS-CoV-2 in ocrelizumab-treated pwMS. Control groups included ocrelizumab-treated pwMS without SARS-CoV-2 infection, and non-MS individuals with and without SARS-CoV-2 infection. Methods: Peripheral blood mononuclear cells were stimulated with SARS-CoV-2 peptide pools and T-cell reactivity was assessed by ELISPOT for interferon (IFN)-γ detection, and by multiparametric fluorescence-activated cell sorting (FACS) analyses for assessment and characterization of T-cell activation. Results: ELISPOT assay against the spike and the N protein of SARS-CoV-2 displayed specific T-cell reactivity in 28/29 (96%) pwMS treated with ocrelizumab and infected by SARS-CoV-2, similar to infected persons without MS. This reactivity was present 1 year after infection and independent from the time of ocrelizumab infusion. FACS analysis following stimulation with SARS-CoV-2 peptide pools showed the presence of activation-induced markers (AIMs) in both CD4 + and CD8 + T-cell subsets in 96% and 92% of these individuals, respectively. Within naïve AIM + CD4 + and CD8 + T-cells, we detected T memory stem cells, suggesting the acquisition of long-term memory. Conclusions: B-cell depletion using ocrelizumab does not impair theBackground: Development of long-lasting anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) T-cell responses in persons with multiple sclerosis (pwMS) treated with ocrelizumab is questioned. Objective: Investigate antiviral T-cell responses after infection with SARS-CoV-2 in ocrelizumab-treated pwMS. Control groups included ocrelizumab-treated pwMS without SARS-CoV-2 infection, and non-MS individuals with and without SARS-CoV-2 infection. Methods: Peripheral blood mononuclear cells were stimulated with SARS-CoV-2 peptide pools and T-cell reactivity was assessed by ELISPOT for interferon (IFN)-γ detection, and by multiparametric fluorescence-activated cell sorting (FACS) analyses for assessment and characterization of T-cell activation. Results: ELISPOT assay against the spike and the N protein of SARS-CoV-2 displayed specific T-cell reactivity in 28/29 (96%) pwMS treated with ocrelizumab and infected by SARS-CoV-2, similar to infected persons without MS. This reactivity was present 1 year after infection and independent from the time of ocrelizumab infusion. FACS analysis following stimulation with SARS-CoV-2 peptide pools showed the presence of activation-induced markers (AIMs) in both CD4 + and CD8 + T-cell subsets in 96% and 92% of these individuals, respectively. Within naïve AIM + CD4 + and CD8 + T-cells, we detected T memory stem cells, suggesting the acquisition of long-term memory. Conclusions: B-cell depletion using ocrelizumab does not impair the development of long-lasting anti-SARS-CoV-2 T-cell responses. … (more)
- Is Part Of:
- Multiple sclerosis. Volume 28:Number 12(2022)
- Journal:
- Multiple sclerosis
- Issue:
- Volume 28:Number 12(2022)
- Issue Display:
- Volume 28, Issue 12 (2022)
- Year:
- 2022
- Volume:
- 28
- Issue:
- 12
- Issue Sort Value:
- 2022-0028-0012-0000
- Page Start:
- 1937
- Page End:
- 1943
- Publication Date:
- 2022-10
- Subjects:
- COVID-19 -- multiple sclerosis -- anti-CD20 -- ocrelizumab -- SARS-CoV-2 -- cellular immune response
Central nervous system -- Diseases -- Periodicals
Myelin sheath -- Diseases -- Periodicals
Inflammation -- Periodicals
Multiple sclerosis -- Periodicals
Central Nervous System Diseases -- Periodicals
Demyelinating Diseases -- Periodicals
Inflammation -- Periodicals
Multiple Sclerosis -- Periodicals
Système nerveux central -- Maladies -- Périodiques
Gaine de myéline -- Maladies -- Périodiques
Inflammation (Pathologie) -- Périodiques
Sclérose en plaques -- Périodiques
Electronic journals
616.834005 - Journal URLs:
- http://msj.sagepub.com/ ↗
http://search.ebscohost.com/login.aspx?direct=true&db=a2h&jid=DZL&site=ehost-live ↗
http://www.uk.sagepub.com/home.nav ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1352-4585;screen=info;ECOIP ↗
http://www.arnoldpublishers.com/journals/pages/mul_scl/13524585.htm ↗ - DOI:
- 10.1177/13524585221102158 ↗
- Languages:
- English
- ISSNs:
- 1352-4585
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22997.xml