Acute relapse and poor immunization following COVID-19 vaccination in a rituximab-treated multiple sclerosis patient.
COVID-19
COVID-19 vaccines
SARS-CoV-2
multiple sclerosis
vaccines
Journal
Human vaccines & immunotherapeutics
ISSN: 2164-554X
Titre abrégé: Hum Vaccin Immunother
Pays: United States
ID NLM: 101572652
Informations de publication
Date de publication:
03 Oct 2021
03 Oct 2021
Historique:
pubmed:
21
5
2021
medline:
16
9
2021
entrez:
20
5
2021
Statut:
ppublish
Résumé
With the progress of COVID-19 vaccination programs worldwide, some new adverse events associated with the available vaccines may unfold, especially in subpopulations, representatives of whom were not included in phase I, II, and III clinical trials of these vaccines, such as patients with autoimmune diseases, including multiple sclerosis (MS). A 34-year-old woman presented with severe right hemiplegia and ataxia. She was diagnosed with relapsing-remitting MS (RRMS) 13 years ago and treated with rituximab (an anti-CD20 monoclonal antibody) during the last 15 months. She had received her first dose of adenovirus-vectored COVID-19 vaccine Gam-COVID-Vac (Sputnik V) three months after her last infusion of rituximab and three days before experiencing her latest MS relapse episode, preceded by mild symptoms (fatigue, myalgia, generalized weakness, etc.). Magnetic resonance imaging revealed several new periventricular, juxtacortical, brainstem, and cerebellar peduncle lesions. She received corticosteroid therapy for five consecutive days, and her neurological deficits slightly improved. Twenty-one days after receiving the first dose of the vaccine, her anti-SARS-CoV-2 antibodies were below the lower detection limit. However, a decision was made to adhere to the vaccination schedule and not risk the patient's safety against an unfortunate COVID-19 contraction, and thus, she was advised to receive the second Gam-COVID-Vac dose after discontinuation of oral steroid taper. The safety of adenovirus-based vaccines in patients with autoimmune diseases requires further investigation. Meanwhile, clinicians should raise awareness among their patients regarding the potentially limited efficacy of COVID-19 vaccination in those treated with anti-CD20 treatments. After careful, individualized risk-benefit assessments, planning a delay/pause in such treatments to create a time window for patients to receive the vaccine and develop anti-SARS-CoV-2 immunity may be recommended.
Identifiants
pubmed: 34015240
doi: 10.1080/21645515.2021.1928463
pmc: PMC8437516
doi:
Substances chimiques
COVID-19 Vaccines
0
Rituximab
4F4X42SYQ6
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3481-3483Références
Cell Rep Med. 2020 Jun 23;1(3):100040
pubmed: 32835303
Lancet. 2021 Jan 9;397(10269):99-111
pubmed: 33306989
Mol Ther. 2020 Nov 4;28(11):2303-2304
pubmed: 33065038
JAMA. 2021 Apr 20;325(15):1535-1544
pubmed: 33704352
Lancet. 2021 Feb 20;397(10275):671-681
pubmed: 33545094
J Neurol. 2021 Apr 12;:
pubmed: 33844056
Clin Exp Immunol. 2020 Nov;202(2):149-161
pubmed: 32671831
Mult Scler Relat Disord. 2020 Nov;46:102482
pubmed: 32916509
J Neurol. 2021 Jan 8;:
pubmed: 33416999