Evidence map›Paper›PMID 39266969›Full record

ArticleBMC infectious diseases2024

Longevity of hybrid immunity against SARS-CoV-2 in adults vaccinated with an adenovirus-based COVID-19 vaccine.

Memory Mvula, Fatima Mtonga, Jonathan Mandolo, Chisomo Jowati, Alice Kalirani, Precious Chigamba, Edwin Lisimba, Ndaona Mitole, Marah G Chibwana, Kondwani C Jambo

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Memory MvulaMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Fatima MtongaMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Jonathan MandoloMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Chisomo JowatiMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Alice KaliraniMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Precious ChigambaMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Edwin LisimbaMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Ndaona MitoleMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Marah G ChibwanaMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi.
Kondwani C JamboMalawi-Liverpool-Wellcome Research Programme, Blantyre, Malawi. Kondwani.Jambo@lstmed.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundHybrid immunity provides better protection against COVID-19 than vaccination or prior natural infection alone. It induces high magnitude and broadly cross-reactive neutralising anti-Spike IgG antibodies. However, it is not clear how long these potent antibodies last, especially in the context of adenovirus-based COVID-19 vaccines.

methodsWe conducted a longitudinal cohort study and enrolled 20 adults who had received an adenovirus-based COVID-19 vaccine before a laboratory-confirmed SARS-CoV-2 infection. We followed up the study participants for 390 days post the initial breakthrough infection. We assessed the longevity and cross-reactive breadth of serum antibodies against SARS-CoV-2 variants of concern (VOCs), including Omicron.

resultsThe binding anti-Spike IgG antibodies remained within the reported putative levels for at least 360 days and were cross-neutralising against Beta, Gamma, Delta, and Omicron. During the follow up period, a median of one SARS-CoV-2 re-infection event was observed across the cohort, but none resulted in severe COVID-19. Moreover, the re-exposure events were associated with augmented anti-Spike and anti-RBD IgG antibody titres.

conclusionsThis study confirms that hybrid immunity provides durable broadly cross-reactive antibody immunity against SARS-CoV-2 variants of concern for at least a year (360 days), and that it is further augment by SARS-CoV-2 re-exposure.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19COVID-19 VaccinesCross ReactionsImmunoglobulin GSARS-CoV-2AdenoviridaeAdultAgedCohort StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, CoronavirusBreakthrough infectionHybrid immunityLongevitySARS-CoV-2

Identifiers

PMID39266969
PMCPMC11391831

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LicenceCC BY
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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.