Evidence map›Paper›PMID 36059537›Full record

ArticleFrontiers in immunology2022

Cross-sectional analysis of the humoral response after SARS-CoV-2 vaccination in Sardinian multiple sclerosis patients, a follow-up study.

Maria Laura Idda, Maristella Pitzalis, Valeria Lodde, Annalisa Loizedda, Jessica Frau, Monia Lobina, Magdalena Zoledziewska, Francesca Virdis, Giuseppe Delogu, Maria Giuseppina Marini and 19 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Circular RNAs in Immune-Related Diseases.Advances in experimental medicine and biology · 2025
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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

29 authors at 6 institutions in 1 country.

Maria Laura IddaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Maristella PitzalisInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Valeria LoddeDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Annalisa LoizeddaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Jessica FrauRegional Multiple Sclerosis Center, Azienda Sanitaria Locale (ASL) Cagliari, Cagliari, Italy.
Monia LobinaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Magdalena ZoledziewskaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Francesca VirdisInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Giuseppe DeloguDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Maria Giuseppina MariniInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Maura MingoiaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Marco MasalaInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Lorena LoreficeRegional Multiple Sclerosis Center, Azienda Sanitaria Locale (ASL) Cagliari, Cagliari, Italy.
Marzia FronzaDepartment of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Daniele CarmagniniDepartment of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Elisa CartaDepartment of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Silvy PilottoDepartment of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Paolo CastigliaDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari, Italy.
Paola ChessaDepartment of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Sergio UzzauDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Gabriele FarinaNeurology Unit, Azienza Ospedaliera Universitaria (AOU) Sassari, Sassari, Italy.
Paolo SollaDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari, Italy.
Maristella SteriInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Marcella DevotoInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Edoardo FiorilloInstitute for Genetic and Biomedical Research, National Research Council, Cagliari, Italy.
Matteo FlorisDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Roberto Ignazio ZarboDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari, Italy.
Eleonora CoccoRegional Multiple Sclerosis Center, Azienda Sanitaria Locale (ASL) Cagliari, Cagliari, Italy.
Francesco CuccaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
National Research Council · ITUniversity of Sassari · ITUniversity of Cagliari · ITInstitute of Genetic and Biomedical Research · ITASL Roma · ITAzienda Ospedaliero Universitaria di Sassari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring immune responses to SARS-CoV-2 vaccination and its clinical efficacy over time in Multiple Sclerosis (MS) patients treated with disease-modifying therapies (DMTs) help to establish the optimal strategies to ensure adequate COVID-19 protection without compromising disease control offered by DMTs. Following our previous observations on the humoral response one month after two doses of BNT162b2 vaccine (T1) in MS patients differently treated, here we present a cross-sectional and longitudinal follow-up analysis six months following vaccination (T2, n=662) and one month following the first booster (T3, n=185). Consistent with results at T1, humoral responses were decreased in MS patients treated with fingolimod and anti-CD20 therapies compared with untreated patients also at the time points considered here (T2 and T3). Interestingly, a strong upregulation one month after the booster was observed in patients under every DMTs analyzed, including those treated with fingolimod and anti-CD20 therapies. Although patients taking these latter therapies had a higher rate of COVID-19 infection five months after the first booster, only mild symptoms that did not require hospitalization were reported for all the DMTs analyzed here. Based on these findings we anticipate that additional vaccine booster shots will likely further improve immune responses and COVID-19 protection in MS patients treated with any DMT.

Indexed as

COVID-19Multiple SclerosisBNT162 VaccineCOVID-19 VaccinesCross-Sectional StudiesFingolimod HydrochlorideFollow-Up StudiesHumansSARS-CoV-2VaccinationBNT162 VaccineCOVID-19 VaccinesFingolimod HydrochlorideBNT162b2 messenger RNA (mRNA)COVID-19COVID-19 vaccinationdisease-modifying therapy (DMT)humoral immunitymultiple sclerosisSARS-CoV-2vaccine efficacy and effectiveness

Identifiers

PMID36059537
PMCPMC9433902
OpenAlexW4292416123

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.