Evidence map›Paper›PMID 35389888›Full record

ArticleJCI insight2022

SARS-CoV-2-specific immune responses in boosted vaccine recipients with breakthrough infections during the Omicron variant surge.

Bezawit A Woldemeskel, Caroline C Garliss, Tihitina Y Aytenfisu, Trevor S Johnston, Evan J Beck, Arbor G Dykema, Nicole Frumento, Desiree A Wright, Andrew H Yang, Alexander I Damanakis and 5 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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

15 authors at 3 institutions in 2 countries.

Bezawit A WoldemeskelDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Caroline C GarlissDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Tihitina Y AytenfisuDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Trevor S JohnstonDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Evan J BeckDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Arbor G DykemaThe Bloomberg~Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA.
Nicole FrumentoDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Desiree A WrightDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Andrew H YangThe Bloomberg~Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA.
Alexander I DamanakisDepartment of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Oliver LaeyendeckerDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Andrea L CoxDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Heba H MostafaDepartment of Pathology, Division of Medical Microbiology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Andrew H KarabaDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Joel N BlanksonDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USBloomberg (United States) · USNational Institute of Allergy and Infectious Diseases · US

Funding

HOPE in Action: A Clinical Trial of HIV-to-HIV Liver TransplantationU01AI138897 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Christine Marie Durand, DORRY L. SEGEV · 2018 to 2026
$25.5M
Medical Scientist Training ProgramT32GM136577 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ANDREA L COX · 2020 to 2026
$13.4M
Virology Resource CoreU54CA260492 · NCI · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L, KLEIN, SABRA L. · 2020 to 2024
$10.4M
Modulation of Herpes Simplex Virus Pathogenesis by Leucine Rich Repeat Kinase 2K08AI156021 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KARABA, ANDREW HOOVER · 2021 to 2025
$994k
Epidemiologic and Immunologic Investigations of SARS-CoV-2 (COVID-19) InfectionsZIAAI001286 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI QUINN, THOMAS · 2020 to 2023
$349k
NCI NIH HHS U54 CA260492NIAID NIH HHS K08 AI156021NIAID NIH HHS U01 AI138897NIGMS NIH HHS T32 GM136577
6 · The paper itself

Abstract

BackgroundBreakthrough SARS-CoV-2 infections in vaccinated individuals have been previously associated with suboptimal humoral immunity. However, less is known about breakthrough infections with the Omicron variant.MethodsWe analyzed SARS-CoV-2-specific antibody and cellular responses in healthy vaccine recipients who experienced breakthrough infections a median of 50 days after receiving a booster mRNA vaccine with an ACE2 binding inhibition assay and an ELISpot assay, respectively.ResultsWe found that high levels of antibodies inhibited vaccine strain spike protein binding to ACE2 but that lower levels inhibited Omicron variant spike protein binding to ACE2 in 4 boosted vaccine recipients prior to infection. The levels of antibodies that inhibited vaccine strain and Omicron spike protein binding after breakthrough in 18 boosted vaccine recipients were similar to levels seen in COVID-19-negative boosted vaccine recipients. In contrast, boosted vaccine recipients had significantly stronger T cell responses to both vaccine strain and Omicron variant spike proteins at the time of breakthrough.ConclusionOur data suggest that breakthrough infections with the Omicron variant can occur despite robust immune responses to the vaccine strain spike protein.FundingThis work was supported by the Johns Hopkins COVID-19 Vaccine-related Research Fund and by funds from the National Institute of Allergy and Infectious Disease intramural program as well as awards from the National Cancer Institute (U54CA260491) and the National Institutes of Allergy and Infectious Disease (K08AI156021 and U01AI138897).

Indexed as

Communicable DiseasesCOVID-19HypersensitivityAngiotensin-Converting Enzyme 2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansImmunitymRNA VaccinesSARS-CoV-2Vaccines, SyntheticAngiotensin-Converting Enzyme 2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesmRNA VaccinesVaccines, SyntheticAdaptive immunityCOVID-19T cells

Identifiers

PMID35389888
PMCPMC9220829
OpenAlexW4225543484

What OpenQuestion holds

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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.