Evidence map›Paper›PMID 35334278›Full record

ArticleMultiple sclerosis and related disorders2022

Persistently reduced humoral and sustained cellular immune response from first to third SARS-CoV-2 mRNA vaccination in anti-CD20-treated multiple sclerosis patients.

Hamza Mahmood Bajwa, Frederik Novak, Anna Christine Nilsson, Christian Nielsen, Dorte K Holm, Kamilla Østergaard, Agnes Hauschultz Witt, Keld-Erik Byg, Isik S Johansen, Kristen Mittl and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Hamza Mahmood BajwaDepartment of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Frederik NovakDepartment of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Anna Christine NilssonDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Christian NielsenDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark.
Dorte K HolmDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark.
Kamilla ØstergaardDepartment of Neurology, Nordsjællands Hospital, Hillerød, Denmark.
Agnes Hauschultz WittDepartment of Neurology, Hospitalsenhed Midt, Viborg, Denmark.
Keld-Erik BygDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Rheumatology, Odense University Hospital, Odense, Denmark.
Isik S JohansenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Kristen MittlWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, USA.
William RowlesWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, USA.
Scott S ZamvilWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, USA.
Riley BoveWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, USA.
Joseph J SabatinoWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, USA.
Tobias SejbaekDepartment of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark. Electronic address: tobias.sejbaek@rsyd.dk.
University of Southern Denmark · DKUniversity of California, San Francisco · USOdense University Hospital · DKNordsjællands Hospital · DKRegional Hospital Central Jutland · DK

Funding

Repertoire selection of AQP4-specific T cells that cause CNS autoimmunediseaseR01AI131624 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAMVIL, SCOTT S · 2019 to 2023
$2.2M
NIAID NIH HHS R01 AI131624
6 · The paper itself

Abstract

objectiveTo examine humoral and cellular response in multiple sclerosis patients on anti-CD20 therapy after third BNT162b2 mRNA SARS-CoV-2 vaccination.

methodsA prospective longitudinal study design from first throughout third vaccination in Danish and American MS centers. All participants were treated with ocrelizumab. Antibody (Ab) levels were assessed before and after third vaccination using SARS-CoV-2 IgG II Quant assay (Abbott Laboratories). B- and T-lymphocytes enumeration was done with BD Multitest™6-color TBNK reagent. Spike-specific T-cell responses were measured through PBMC stimulation with spike peptide pools (JPT Peptide Technologies).

resultsWe found that 14.0%, 37.7%, and 33.3% were seropositive after first, second and third vaccination. The median Ab-levels were 74.2 BAU/mL (range: 8.5-2427) after second vaccination, as well as 43.7 BAU/ml (range: 7.8-366.1) and 31.3 BAU/mL (range: 7.9-507.0) before and after third vaccination, respectively. No difference was found in levels after second and third vaccination (p = 0.1475). Seropositivity dropped to 25.0% of participants before the third vaccination, a relative reduction of 33.3% (p = 0.0020). No difference was found between frequencies of spike reactive CD4

conclusionIn this longitudinal cohort we found no significant increased humoral or cellular response with administration of a third SARS-CoV-2 mRNA vaccination. These findings suggest the need for clinical strategies to include allowance of B cell reconstitution before repeat vaccination and/or provision of pre-exposure prophylactic monoclonal antibodies.

Indexed as

COVID-19Multiple SclerosisAntibodies, ViralAntigens, CD20BNT162 VaccineCD8-Positive T-LymphocytesCOVID-19 VaccinesHumansImmunity, CellularLeukocytes, MononuclearLongitudinal StudiesProspective StudiesRNA, MessengerSARS-CoV-2VaccinationAntibodies, ViralAntigens, CD20BNT162 VaccineCOVID-19 VaccinesRNA, MessengerAntibody responseAnti-CD20BNT162b2Booster vaccinemRNA vaccineMultiple sclerosisOcrelizumabSARS-CoV-2

Identifiers

PMID35334278
PMCPMC8898195
OpenAlexW4220825786

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.