B- and T-Cell Responses After SARS-CoV-2 Vaccination in Patients With Multiple Sclerosis Receiving Disease Modifying Therapies: Immunological Patterns and Clinical Implications.
CD20
COVID
IGRA
T-lymphocyte
fingolimod
natalizumab
ocrelizumab
peptides
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
16
10
2021
accepted:
24
12
2021
entrez:
3
2
2022
pubmed:
4
2
2022
medline:
8
2
2022
Statut:
epublish
Résumé
Vaccination campaign to contrast the spread of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has raised the issue of vaccine immunogenicity in special populations such as people with multiple sclerosis (PwMS) on highly effective disease modifying treatments (DMTs). While humoral responses to SARS-CoV-2 mRNA vaccines have been well characterized in the general population and in PwMS, very little is known about cell-mediated responses in conferring protection from SARS-CoV-2 infection and severe coronavirus disease-2019 (COVID-19). PwMS on ocrelizumab, fingolimod or natalizumab, vaccinated with two doses of mRNABNT162b2 (Comirnaty Thirty PwMS and 9 HDs were enrolled. All the patients were negative for anti-N antibody detection, nor reported previous symptoms of COVID-19. Peripheral blood lymphocyte counts were assessed in PwMS showing: (i) reduction of circulating B-lymphocytes in PwMS on ocrelizumab; (ii) reduction of peripheral blood B- and T-lymphocyte absolute counts in PwMS on fingolimod and (iii) normal B- and T-lymphocyte absolute counts with an increase in circulating CD16+CD56+ NK-cells in PwMS on natalizumab. Three patterns of immunological responses were identified in PwMS. In patients on ocrelizumab, anti-S antibody were lacking or reduced, while T-cell responses were normal. In patients on fingolimod both anti-S titers and T-cell mediated responses were impaired. In patients on natalizumab both anti-S titers and T-cell responses were present and comparable to those observed in HD. The evaluation of T-cell responses, anti-S titers and peripheral blood lymphocyte absolute count in PwMS on DMTs can help to better characterize the immunological response after SARS-CoV-2 vaccination. The evaluation of T-cell responses in longitudinal cohorts of PwMS will help to clarify their protective role in preventing SARS-CoV-2 infection and severe COVID-19. The correlation between DMT treatment and immunological responses to SARS-CoV-2 vaccines could help to better evaluate vaccination strategies in PwMS.
Sections du résumé
Background
Vaccination campaign to contrast the spread of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has raised the issue of vaccine immunogenicity in special populations such as people with multiple sclerosis (PwMS) on highly effective disease modifying treatments (DMTs). While humoral responses to SARS-CoV-2 mRNA vaccines have been well characterized in the general population and in PwMS, very little is known about cell-mediated responses in conferring protection from SARS-CoV-2 infection and severe coronavirus disease-2019 (COVID-19).
Methods
PwMS on ocrelizumab, fingolimod or natalizumab, vaccinated with two doses of mRNABNT162b2 (Comirnaty
Results
Thirty PwMS and 9 HDs were enrolled. All the patients were negative for anti-N antibody detection, nor reported previous symptoms of COVID-19. Peripheral blood lymphocyte counts were assessed in PwMS showing: (i) reduction of circulating B-lymphocytes in PwMS on ocrelizumab; (ii) reduction of peripheral blood B- and T-lymphocyte absolute counts in PwMS on fingolimod and (iii) normal B- and T-lymphocyte absolute counts with an increase in circulating CD16+CD56+ NK-cells in PwMS on natalizumab. Three patterns of immunological responses were identified in PwMS. In patients on ocrelizumab, anti-S antibody were lacking or reduced, while T-cell responses were normal. In patients on fingolimod both anti-S titers and T-cell mediated responses were impaired. In patients on natalizumab both anti-S titers and T-cell responses were present and comparable to those observed in HD.
Conclusions
The evaluation of T-cell responses, anti-S titers and peripheral blood lymphocyte absolute count in PwMS on DMTs can help to better characterize the immunological response after SARS-CoV-2 vaccination. The evaluation of T-cell responses in longitudinal cohorts of PwMS will help to clarify their protective role in preventing SARS-CoV-2 infection and severe COVID-19. The correlation between DMT treatment and immunological responses to SARS-CoV-2 vaccines could help to better evaluate vaccination strategies in PwMS.
Identifiants
pubmed: 35111162
doi: 10.3389/fimmu.2021.796482
pmc: PMC8801814
doi:
Substances chimiques
BNT162 Vaccine
N38TVC63NU
Types de publication
Clinical Trial
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
796482Informations de copyright
Copyright © 2022 Iannetta, Landi, Cola, Campogiani, Malagnino, Teti, Coppola, Di Lorenzo, Fraboni, Buccisano, Grelli, Mozzani, Zingaropoli, Ciardi, Nisini, Bernardini, Andreoni, Marfia and Sarmati.
Déclaration de conflit d'intérêts
MI received honoraria for lectures from Biogen Italia, AIM Educational, MICOM srl. DL received travel funding from Biogen, Merk-Serono, Sanofi-Genzyme, Teva, speaking or consultation fees from Sanofi-Genzyme, Merk-Serono, Teva, Biogen, Novartis, Roche. LC received honoraria for lectures from MICOM srl. VM received honoraria for lectures from Janssen-Cilag. ET received honoraria for lectures from Gilead, AbbVie and MSD, and research grants from Gilead, outside the submitted work. FB received honoraria for lectures from Novartis. MA reports honoraria for lectures and research grants from Merk, Gilead, Abbvie, Angelini SpA, outside the submitted work. GM is an Advisory Board member of Biogen Idec, Genzyme, Merck-Serono, Novartis, Teva and received honoraria for speaking or consultation fees from Almirall, Bayer Schering, Biogen Idec, Merck Serono, Novartis, Sanofi-Genzyme, Roche, Mylan, Teva. LS reports honoraria for lectures and research grants from Merk, Gilead, Abbvie, Angelini SpA, outside the submitted work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Neurol Neuroimmunol Neuroinflamm. 2021 Jul 28;8(5):
pubmed: 34321333
Mult Scler Relat Disord. 2021 Oct;55:103157
pubmed: 34418737
Mult Scler Relat Disord. 2020 Oct;45:102442
pubmed: 32777745
J Neurol Sci. 2014 Jun 15;341(1-2):22-7
pubmed: 24731783
Vaccine. 2018 Nov 29;36(50):7632-7640
pubmed: 30392766
Respir Res. 2021 Jun 1;22(1):165
pubmed: 34074288
Neurol Res. 2012 Sep;34(7):730-3
pubmed: 22709910
PLoS One. 2021 Jul 27;16(7):e0255316
pubmed: 34314457
Ann Neurol. 2011 Feb;69(2):408-13
pubmed: 21387383
Nature. 2021 Jul;595(7868):572-577
pubmed: 34044428
Ther Adv Neurol Disord. 2021 Aug 13;14:17562864211038111
pubmed: 34413902
Clin Infect Dis. 2021 Nov 2;73(9):e3130-e3132
pubmed: 33035306
Science. 2021 Dec 3;374(6572):abm0829
pubmed: 34648302
Neurology. 2015 Mar 3;84(9):872-9
pubmed: 25636714
Nat Med. 2021 Jul;27(7):1280-1289
pubmed: 34017137
N Engl J Med. 2020 Feb 20;382(8):727-733
pubmed: 31978945
Ther Adv Neurol Disord. 2021 May 29;14:17562864211020082
pubmed: 34104221
Ther Adv Neurol Disord. 2021 Apr 22;14:17562864211012835
pubmed: 34035836
Ann Clin Transl Neurol. 2021 Aug;8(8):1738-1744
pubmed: 34240579
Cell. 2020 Nov 12;183(4):996-1012.e19
pubmed: 33010815
Immunity. 2021 Sep 14;54(9):2133-2142.e3
pubmed: 34453880
Immunol Res. 2021 Dec;69(6):576-583
pubmed: 34417958
EBioMedicine. 2021 Oct;72:103581
pubmed: 34563483
Nat Med. 2021 Nov;27(11):1990-2001
pubmed: 34522051
Nature. 2021 Feb;590(7847):630-634
pubmed: 33276369
JAMA Neurol. 2021 Dec 1;78(12):1510-1514
pubmed: 34554197
JAMA. 2021 Apr 6;325(13):1318-1320
pubmed: 33635317
Nat Rev Immunol. 2020 Aug;20(8):457-458
pubmed: 32636479
Ther Adv Neurol Disord. 2021 May 31;14:17562864211019567
pubmed: 34104219
Sci Rep. 2021 Jun 17;11(1):12762
pubmed: 34140530
Neurology. 2020 Oct 6;95(14):e1999-e2008
pubmed: 32727835
J Neuroimmunol. 2021 Oct 15;359:577696
pubmed: 34418815
Ann Neurol. 2021 Apr;89(4):780-789
pubmed: 33480077