Evidence map›Paper›PMID 35192617›Full record

Trial reportPloS one2022

Durable T-cellular and humoral responses in SARS-CoV-2 hospitalized and community patients.

Kristin G-I Mohn, Geir Bredholt, Fan Zhou, Anders Madsen, Therese B Onyango, Elisabeth B Fjelltveit, Sarah L Jalloh, Karl A Brokstad, Diego Cantoni, Martin Mayora-Neto and 4 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 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
1.5field-weighted citation impact, top 17% 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, 15 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

14 authors at 3 institutions in 2 countries.

Kristin G-I MohnInfluenza Centre, Bergen, Norway.ORCID 0000-0002-3249-1719
Geir BredholtInfluenza Centre, Bergen, Norway.ORCID 0000-0002-8953-8821
Fan ZhouInfluenza Centre, Bergen, Norway.
Anders MadsenInfluenza Centre, Bergen, Norway.
Therese B OnyangoInfluenza Centre, Bergen, Norway.
Elisabeth B FjelltveitInfluenza Centre, Bergen, Norway.
Sarah L JallohInfluenza Centre, Bergen, Norway.
Karl A BrokstadDepartment of Clinical Science, Broegelmann Research Laboratory, University of Bergen, Bergen, Norway.
Diego CantoniViral Pseudotype Unit, Medway School of Pharmacy, University of Kent, Chatham, United Kingdom.ORCID 0000-0001-8527-7719
Martin Mayora-NetoViral Pseudotype Unit, Medway School of Pharmacy, University of Kent, Chatham, United Kingdom.ORCID 0000-0002-5331-5554
Nigel TempertonViral Pseudotype Unit, Medway School of Pharmacy, University of Kent, Chatham, United Kingdom.
Nina LangelandInfluenza Centre, Bergen, Norway.
Rebecca J CoxInfluenza Centre, Bergen, Norway.
Bergen COVID-19 research group
University of Bergen · NOMedway School of Pharmacy · GBWestern Norway University of Applied Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeutralizing antibodies are important for protection against the pandemic SARS-CoV-2 virus, and long-term memory responses determine the risk of re-infection or boosting after vaccination. T-cellular responses are considered important for partial protection against novel variants of concern.

methodsA prospective cohort of hospitalized (n = 14) and community (n = 38) patients with rt-PCR confirmed SARS-CoV-2 infection were recruited. Blood samples and clinical data were collected when diagnosed and at 6 months. Serum samples were analyzed for SARS-CoV-2-spike specific antibodies using ELISA (IgG, IgA, IgM), pseudotype neutralization and microneutralization assays. Peripheral blood mononuclear cells were investigated for virus-specific T-cell responses in the interferon-γ and interleukin-2 fluorescent-linked immunosorbent spot (FluroSpot) assay.

resultsWe found durable SARS-CoV-2 spike- and internal protein specific T-cellular responses in patients with persistent antibodies at 6 months. Significantly higher IL-2 and IFN-γ secreting T-cell responses as well as SARS-CoV-2 specific IgG and neutralizing antibodies were detected in hospitalized compared to community patients. The immune response was impacted by age, gender, comorbidity and severity of illness, reflecting clinical observations.

conclusionsSARS-CoV-2 specific T-cellular and antibody responses persisted for 6 months post confirmed infection. In previously infected patients, re-exposure or vaccination will boost long-term immunity, possibly providing protection against re-infection with variant viruses.

Indexed as

Immunity, CellularAdultAgedAged, 80 and overAge FactorsAntibodies, NeutralizingAntibodies, ViralCOVID-19FemaleFollow-Up StudiesHospitalizationHumansInterferon-gammaInterleukin-2MaleMiddle AgedAntibodies, NeutralizingAntibodies, ViralIFNG protein, humanIL2 protein, humanInterferon-gammaInterleukin-2

Identifiers

PMID35192617
PMCPMC8863217
OpenAlexW4212991545

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.