Evidence map›Paper›PMID 34956211›Full record

ArticleFrontiers in immunology2021

Effect of Different Disease-Modifying Therapies on Humoral Response to BNT162b2 Vaccine in Sardinian Multiple Sclerosis Patients.

Maristella Pitzalis, Maria Laura Idda, Valeria Lodde, Annalisa Loizedda, Monia Lobina, Magdalena Zoledziewska, Francesca Virdis, Giuseppe Delogu, Federica Pirinu, Maria Giuseppina Marini and 17 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
3.4field-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

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 56 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 7 institutions in 1 country.

Maristella PitzalisInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Maria Laura IddaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Valeria LoddeDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Annalisa LoizeddaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Monia LobinaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Magdalena ZoledziewskaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Francesca VirdisInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Giuseppe DeloguDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Federica PirinuDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Maria Giuseppina MariniInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Maura MingoiaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Jessica FrauRegional Multiple Sclerosis Center, Azienda SocioSanitaria Locale (ASSL) Cagliari, Azienda Tutela Salute (ATS) Sardegna, Cagliari, Italy.
Lorena LoreficeRegional Multiple Sclerosis Center, Azienda SocioSanitaria Locale (ASSL) Cagliari, Azienda Tutela Salute (ATS) Sardegna, 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.
Valeria OrrùInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Sergio UzzauDepartment of Biomedical Sciences, University of Sassari - Unit of Clinical Microbiology, Azienza Ospedaliera Universitaria (AOU) Sassari, Sassari, Italy.
Paolo SollaDepartment of Medical, Surgical and Experimental Sciences, University of Sassari - Neurology Unit, Azienza Ospedaliera Universitaria (AOU) Sassari, Sassari, Italy.
Federica LoiOsservatorio Epidemiologico Veterinario Regionale, Istituto Zooprofilattico Sperimentale della Sardegna, Cagliari, Italy.
Marcella DevotoInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Maristella SteriInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Edoardo FiorilloInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
Matteo FlorisDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Ignazio Roberto ZarboDepartment of Medical, Surgical and Experimental Sciences, University of Sassari - Neurology Unit, Azienza Ospedaliera Universitaria (AOU) Sassari, Sassari, Italy.
Eleonora CoccoRegional Multiple Sclerosis Center, Azienda SocioSanitaria Locale (ASSL) Cagliari, Azienda Tutela Salute (ATS) Sardegna, Cagliari, Italy.
Francesco CuccaInstitute for Genetic and Biomedical Research, National Research Council, Monserrato, Cagliari, Italy.
National Research Council · ITInstitute of Genetic and Biomedical Research · ITUniversity of Sassari · ITUniversity of Cagliari · ITATS Sardegna (Italy) · ITAzienda Ospedaliero Universitaria di Sassari · ITIstituto Zooprofilattico Sperimentale della Sardegna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Vaccination against COVID-19 is highly recommended to patients affected by multiple sclerosis (MS); however, the impact of MS disease-modifying therapies (DMTs) on the immune response following vaccination has been only partially investigated. Here, we aimed to elucidate the effect of DMTs on the humoral immune response to mRNA-based anti-SARS-CoV-2 vaccines in MS patients. Methods: We obtained sera from 912 Sardinian MS patients and 63 healthy controls 30 days after the second dose of BNT162b2 vaccine and tested them for SARS-CoV-2 response using anti-Spike (S) protein-based serology. Previous SARS-CoV-2 infection was assessed by anti-Nucleocapsid (N) serology. Patients were either untreated or undergoing treatment with a total of 13 different DMTs. Differences between treatment groups comprised of at least 10 patients were assessed by generalized linear mixed-effects model. Demographic and clinical data and smoking status were analyzed as additional factors potentially influencing humoral immunity from COVID-19 vaccine. Results: MS patients treated with natalizumab, teriflunomide, azathioprine, fingolimod, ocrelizumab, and rituximab showed significantly lower humoral responses compared to untreated patients. We did not observe a statistically significant difference in response between patients treated with the other drugs (dimethyl fumarate, interferon, alemtuzumab and glatiramer acetate) and untreated patients. In addition, older age, male sex and active smoking were significantly associated with lower antibody titers against SARS-CoV-2. MS patients previously infected with SARS-CoV-2 had significantly higher humoral responses to vaccine than uninfected patients. Conclusion: Humoral response to BNT162b2 is significantly influenced by the specific DMTs followed by patients, as well as by other factors such as previous SARS-CoV-2 infection, age, sex, and smoking status. These results are important to inform targeted strategies to prevent clinically relevant COVID-19 in MS patients.

Indexed as

AdultAntibodies, ViralAntirheumatic AgentsBNT162 VaccineCOVID-19FemaleHumansImmunogenicity, VaccineItalyMaleMiddle AgedMultiple SclerosisSARS-CoV-2SeroconversionAntibodies, ViralAntirheumatic AgentsBNT162 VaccineBNT162b2COVID-19disease-modifying therapyhumoral immunitymultiple sclerosisSARS-CoV-2vaccine efficacy

Identifiers

PMID34956211
PMCPMC8697018
OpenAlexW4226119749

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.