Evidence map›Paper›PMID 35359985›Full record

ArticleFrontiers in immunology2022

Long Lasting Cellular Immune Response Induced by mRNA Vaccination: Implication for Prevention Strategies.

Laura Vitiello, Lucia Gatta, Sara Ilari, Stefano Bonassi, Mario Cristina, Filippo Ciatti, Massimo Fini, Stefania Proietti, Patrizia Russo, Carlo Tomino and 1 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 11 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

11 authors at 4 institutions in 1 country.

Laura VitielloLaboratory of Flow Cytometry, IRCCS San Raffaele Roma, Rome, Italy.
Lucia GattaScientific Direction, IRCCS San Raffaele Roma, Rome, Italy.
Sara IlariDepartment of Health Science, Institute of Research for Food Safety and Health (IRC-FSH), University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Stefano BonassiClinical and Molecular Epidemiology, IRCCS San Raffaele Roma, Rome, Italy.
Mario CristinaMEBIC, IRCCS San Raffaele Roma, Rome, Italy.
Filippo CiattiLaboratory of Clinical Pathology, IRCCS San Raffaele Roma, Rome, Italy.
Massimo FiniScientific Direction, IRCCS San Raffaele Roma, Rome, Italy.
Stefania ProiettiClinical and Molecular Epidemiology, IRCCS San Raffaele Roma, Rome, Italy.
Patrizia RussoClinical and Molecular Epidemiology, IRCCS San Raffaele Roma, Rome, Italy.
Carlo TominoScientific Direction, IRCCS San Raffaele Roma, Rome, Italy.
Dolores LimongiDepartment of Human Sciences and Quality of Life Promotion, San Raffaele University, Rome, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITIstituto di Ricovero e Cura a Carattere Scientifico San RaffaeleMagna Graecia University · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the COVID19 pandemic continues to spread and vaccinations are administered throughout the world at different rates and with different strategies, understanding the multiple aspects of the immune response to vaccinations is required to define more efficient vaccination strategies. To date, the duration of protection induced by COVID19 vaccines is still matter of debate. To assess whether 2-doses vaccination with BNT162b2 mRNA COVID-19 vaccine was sufficient to induce a persistent specific cellular immune response, we evaluated the presence of SARS-COV2 Spike-specific B and T lymphocytes in 28 healthcare workers 1 and 7 months after completing the vaccination cycle. The results showed that at 7 months after second dose a population of Spike-specific B lymphocytes was still present in 86% of the immunized subjects, with a higher frequency when compared to not-immunized controls (0.38% ± 0.07 vs 0.13% ± 0.03, p<0.001). Similarly, specific CD4+ and CD8+ T lymphocytes, able to respond

Indexed as

COVID-19COVID-19 VaccinesBNT162 VaccineHumansImmunity, CellularRNA, MessengerRNA, ViralSARS-CoV-2VaccinationBNT162 VaccineCOVID-19 VaccinesRNA, MessengerRNA, ViralB lymphocytesCOVID-19mRNA vaccinationSARS-CoV2T lymphocytes activation

Identifiers

PMID35359985
PMCPMC8961295
OpenAlexW4220969061

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.